Disclosure to Promote the Right To Information

Whereas the Parliament of India has set out to provide a practical regime of right to
information for citizens to secure access to information under the control of public authorities,
in order to promote transparency and accountability in the working of every public authority,
and whereas the attached publication of the Bureau of Indian Standards is of particular interest
to the public, particularly disadvantaged communities and those engaged in the pursuit of
education and knowledge, the attached public safety standard is made available to promote the
timely dissemination of this information in an accurate manner to the public.
1 +, 1 +

01 ' 5

The Right to Information, The Right to Live

Step Out From the Old to the New

Mazdoor Kisan Shakti Sangathan

Jawaharlal Nehru

IS 885 (1994): Common Names for Pesticides and other

Agrochemicals (Excluding Fertilizers) [FAD 1: Pesticides
and Pesticides Residue Analysis]

! $ ' +-
Satyanarayan Gangaram Pitroda

Invent a New India Using Knowledge

! > 0 B

BharthariNtiatakam

Knowledge is such a treasure which cannot be stolen

( Reaffirmed 2004 )

2009

Indian Standard

COMMON NAMESFORPESTICIDESAND OTHER

AGROCHEMTCALS (EXCLUDINGFERTILIZERS)
( Second Revision )

UDC 632.951 COM

Q BIS 1994

BUREAU

OF

INDIAN

STANDARDS

MANAK BHAVAN, 9 BAHADUR SHAH ZAFAR MARG

NEW DELHI 110002
July 1994

Price Group 15

Pesticides Sectional Committee, FAD 1

FOREWORD
This Indian Standard was adopted by the Bureau of Indian Standards, after the draft finalized by the
Pesticides Sectional Committee had been approved by the Food and Agriculture Division Council.
This standard lists the common names of certain pesticides and other agrochemicals used in agriculture,
animal husbandry and public health.
This Indian Standard was first issued in 1956. The first revision was brought out in 1967. This second
revision is being brought out incorporating common names of several chemicals being used in the country
and also to bring the standard in line with the international work being done in this field. In this
revision, effort has been made to prepare a list of chemicals that do not require common names.
The common names used in this standard are the chemical names, in conformity with the English rules
of the International Union of Pure and Applied Chemistry ( IUPAC ) and the International Organization for Standard ( IS0 ), wherever, common names approved by IUPAC and IS0 do not exist, names
as listed in the Chemical Abstracts has been included in this standard.
In the preparation of this standard, reference has been made to the following publications:
IS0 257 : 1976 Pest control chemicals and plant growth regulators - Principles for the selection
of common names.
IS0 765 : 1976 Pesticides considered not to require common names.
IS0 1750 : 1981 cPesticides and other agro chemicals - Common names.
The Pesticide Manual, Seventh Edition, 1983. The British Crop Protection Council, Croydon CR0
2TD.

IS 885 : 1994

Indian Standard

COMMONNAMESFOR PESTICIDESANDOTHER
AGROCHEMICALS [EXCLUDINGFERTILIZERS]
( Second Revision )
1 SCOPE
1.1 This standard comprises of an alphabetical list of
common names for pesticides and other agrochemicals
(excluding fertilizers), together with their correspond:
ing chemical names, structural and molecular formulae
and use.
1.2 This standard also contains a list of chemicals
which have been considered not to require common
natnes.
2 OBJECTIVE .

Acommon name is to provide a short, easily pronounciable name for a compound, whose full chemical name
is too long and complicated, for use in commerce,
industry, official regulations and specifications.
3 PRINCIPLES FOR SELECTION OF
COMMON NAMES
3.1 The common names shall be written or printed in
lower case letters, for example, malathion.
3.2 In the exceptional cases where the names are
formed from the initials, they shall be written in capitals
without intervening full stop, for example, BHC.
3.3 When numerals and letters both occur in a common
name, the numerals shall be started from one another
by commas and from letters (capitals only) by a hyphen,
for example, 2,4-D.
3.4 The common name shall normally apply to the pure
chemical of known structure, but in exceptional cases
it may be given to a mixture of isomers, in which not

all. the isomers may have established biological

activities, for example, BHC.
3.5 Consideration may be given to the coining of
common names for reaction products having an
incompletely defined chemical composition but not for
deliberate mixture of active ingredients.
3.6 A proprietary name shall not be considered as a
commc& name unless the manufacturer has formally
agreed to:
a) not to use it as a.trade-mark; and
b) to permit its use as a common name by giving
up rights to it by any other means conforming
to the statutory provisions.
4 USE
The use of each compound is given according to the
following classification:
Acaricide = A
Molluscicide
=M
Bactericide = B
Nematicide
=N
F u n g i c i d e = F Plant growth regulalors = P
Herbicide = H
Rodenticide
=R
=\
Insecticide = I
Avicide

5 COMMON NAMES
5.1 The common names of different pesticides and
other agrochemicals (excluding fertilizers) have been
listed in Table 1 in an alphabetical order.
5.2 The chemicals considered not to requiie common
names have been listed at Annex A.

Table 1 Common Names for Pest Control Chemicals

( Clause 5.1)
Sl No.

Common Name

(1)

(2)

Use

Chemical Name

(3)

Chemical Structure

(4)

1.

acephate phoramidothioate

0, S-dimethyl acetylphos =

2.

acrylonitrile

acrylonitrile

CH3 S

Cz =

3.

alachlor

2-chloro-2, 6-diethyl
N- methoxymethylacetanilide

4.

aldicarb

2-methyl-2-(methylthio) =

(6)

L - N H y---COCtr~

CH3_0 >

propionaldehyde
carbnmoyloxime

Molecular Formula

C.-_CN

C4HI,,NOjPS

C,H3N

CzHs
C14 %o GINO,

FH3

O-methyl CH3:S -_c - CH = N - O- CO -NH - CH3

I

C7H14N202S

CH3
5.

aldrin

Product containing 95% of HHDN

(see Sl No. 194)
.

C1 2H9C16

CH 3

CH 3

CH2CH = C H ,

C=CH
6.

allethrin

(MS)-3-allyl-2-methyl-4oxocyclopent- 2enyl (lRS)- ck-transchrysanthemate

CH 3

CH 3

0
c19H2603

,alphamethrin

(S)-a&a-cyano-3-phenoxybenzyl

(1 R, 3R)-3(2,2_dichlorovinyl)-2
2-dimethylcyclopropanecarboxyIate
and
(R)-alpha-cyano-3-phenoxybenzyl
(1 S, 3S)-3-(2,2-dichlorovinyl)-2,
2dimenthylcyclopropanecarboxvlatc
in the ratio 1 : 1

CH3S u;& NHCH,CH,

8.

ametryne

C9HuN5S

N-ethyl-N-isopropyl-6 methylthio-I,
3,5-triazine -2,4-diyldiamine

NHCH(CH,),

9.

amidithion

C,H,,NO&

S-2-methoxyethylcarbamoyl =

methyl 0, Odimenthyl phospho =

dithioate

(CH30)2;-S-CHZ-CO

- N H -CH2-CH2-0CH3

s
i

Table 1 ( Corrt@w/

S1 No.

Common Name

(1)

(2)

Use

.=

Chemical Name

(3)

Chemical Structure

(4)

Molecular Forsnuln

(9

(6)

CH3

10.

amitraz

N-methylbis (2, +xylyliminu

CH3

CH3 - /

methyl] wninc

C19H23N3

N=

CHNCH=N

~H3

CH3

.!/
/N\
-

11.

amitm[e

3-ii t71ir10- 1}/-1,

2,

4-traizole

1(

N.
12.

NH 2
anilofos

Ii

~..

S-44kwo-N-isopropyl
=
carbaniloyhnclhyl
O.
O-dimetlwl

C,3H1QCIN03PS3

CI

[Jhosp}~]rt}n~dltl]lotitc

/_\

~COoCli#(OCH3)

-o-

CH(CH ~2

&

13.

antu

.!!IHC.S6NH2
R

1-(1-naphthyI)-2-thiourea

)
@\/
14.

asularn

11

methyl sulphimil ylcarbamate

\
I

Hz~

/
G

15.

altwine

24c~m-4*ttiyloarltiti-tipmpylamin
0-1,3, S-triazine

~02_

~H_~Q

OCH3

(CI+3 )2CH

NH

c1

YN)
N /N
Y
NH C2H5

CJ+10N204S

*
z

..
m
m,
x

Iii.

.
azvnethiphos

C..HIOCIN:O+S

3dih@o-2*xn.$6-chloro-2,
OXWOIO-[4, 5-4 pyridin-11-ylmethyl

0,0-ctirnell@ phosphnmlhiwte]

iXi2!W(OCH3)2

17.

18.

hydm-&oxcJwmo-

azinphos

S-[.3,

ethyl

[d] [1, 2,3] triazin-3-@wthyl) 0,0diethyl phosphorodithmate

azinptws

S(3. 4dihydro-4+xo@w.o

methyl

mi;win-3-vIrnethyl) O, CWmethyl
phosphorodiothioale

bartxm

d-chlombut-2-ynyl
Ialc

J-di

[d] [1,2,3]

m
19.

3-chlorocarbani-

./~
Q
-

NH CO0CI+2C==C

CI

20.

benalaxyl

I?

rncthyl N-phcnylacetyl-N-Z
DL- idanillate

6-xylyl-

/ J
0\
.-..

cti3;
~~2~~\

&j_~3

N
CH3

CH ~

o J
21.

bendkwarb

-d

2,2-dimeihyl-1, 3Aenwdioxol-4-yl
rncthylcarbatrliite

:}
. c
Q)(

0
CH3
& . ...Cj--.-...NH ct+~

CI+2CI

c~#Igclyl:

t;

Tabk 1 (Continued)
S1 No.

Common Name

-,

(1)

(4

22.

henodanil

Use

(3)
I:

Molecuk- Formula

Chemical Structure

Chemical Name

(61

(5)

(2%;

Q-

Z-iodobenzanilide

CO____N

q-J

%HldNO

co- NH(CH&CH,
23.

24.

2.5.

26.

benomyl

bensulide

bentazone

benzoylpropethyl

l-(butylcarbamoyl)
methyl
zimidazol- 2-ylcarbamate

ben-

S-2-benzenesulphonamidoethyl 0, Odi-isoprophyl phosphrodithioate

3-isopropyl-Q-H)-benzo-7
1 ,
thiadiazin-&one 2.2-dioxide

ethyl-N-benzoyl-IV
(3,
dichlorophenyl)- DL-alaninate

C14WJ403

NH - CO - OCHs

o/

C,,H,,NO,PS, ^

SO,-NH-

3-

4-

o-

./
-

Cl-i3

co

LHCO-oCH, CH 3
IN/

3
oI

Cl

.E.

27.

bcnzethiazumn

(JY

LbenzothiazoI-2yI-3 -mctiyluma

:1

CO NHCH3

NH

i
o

c1

29

13HC

(.2
I

1, 2, 3, 4, 5, 6-hexachlorocydo
hcxane (Mixed isomcra)

cl

cl

cl

29.

binapacryl

A
F

2-sec-butyl-4,
6-dinitrophenyl
methyl but-2-enoate

,NQ2
.

3-

-Q-

02N

K. \

0-CO-CH=C(CH3)2
,

\cHc2H 5
tH3

3(?.

bitertanol

aU-mc-l+iphenyj 4yk@-3,

dimethyl-l<w-1,
2, 4..tnazol.l-y?j
butane-2@l [ratio of raceinatea (M/S,
2Rs) and (MS. Xl?) is about 20: 80]

-4

m
/

o-7H4H-c(cH3)3
N\
IjJ

31.

IWMC

2-sec-butylphenyl methykwbarnate

;,.,
0

CH3NHC0-~

- fN3

&H-CH2-CH3

..

Table 1 ( Continued)
!<I No.

Common Name

Use

Chemical Structure

Chemical Name

32.

brodifacoum

3-[3-(l-bromobiphenyL4-yl)-1,
Metrtmhgdro-1-naphthyl]-4hydroxycoumarin

2, 3,

33.

bromacil

5bromo-3-set-butyl-6-methyluracil

34.

bromadiolone

3-[3-(4-bromobiphenyM-yI)-3-hydw
xy-l-phenylpropyll- 4
hydroxycoumarin

35.

bromophos

0-4-bromo-2,5dichlorophenyl 0, O- _
dimethyl phosphorothioate

Molecular Formula

B
..

36.

hromophos-ethyl

0-4-bromo-2, 5-dicholorophenyl 0 ,
0-diethyl phosphorothioate

Br

Cl
37.

bromopropylate

isopropyl 1, -I-dibromobenzilate

OH

CN
38.

bromoxynil

3,5-dibromo-+hvdroxvbenzonitrilc
_

C$IiBr2N0

Br

Br
OH

3Y.

brompyrazon

5-amino-4-bromo-2-phenylpyridazin-3
(2H)-one

lo.

bufenwrb

An isomeric rextion mixture contain-

ing approximately 3 parts by mass 01.

(i) j-(1-methylbutyl) phenyl meth+
carbamate and 1 part by mass of (ii)
3-(1-ethyl=propyl) phenyl methylwrbama te

Table 1 ( Continrred >

Sl No.

Common Name

IJse
(3)

Chemical Name

Chemical Structure

Molecular

:.

Formula

(1)

(2)

41.

buprofczin

2-tert-butylimino-3-isopropyl-5-phe
nyl-1,3,5thiadiazinan&one

Ct,H2,N,0S

42.

butachlor

N-butoxymethyl-2-chloro-2,
6-diethyl=acetanilide

C,,H,~CINO~

43.

buturon

I-1

3-(4-chlorophenyl)-l-methyl-l-( l-m
ethyl = prop-2-ynyl) urea

44.

butylate

S-ethyl di-isobutyl (thiocarbanl.ltc

(4)

(6)

CH, .
NH-CO-Nd-HC=CH

[(CH,)2CHCH2]2-NCO- S-CH2-CH,

C,,II,,CINIO

Ci ,H23NOS

0
45.

captafol

2-tetrachloroetylthioj
N-(1, 1, 2,
cyclohex-4-ene-1,2- dicarboximide

0
46.

captan

1V-(trichloromethylthio)
ene-1,2-dicarboximide

cyclohex-4-

-CHCI 2

C,,H,CI,NO,S

C,II,CI,NOZS

E
3E
01
..
5

OCO-NHCH,

48.

carbendazim

2 NH-CO-OCH,

methyl benzimidazol-7-yI~mdmate

OCO-NHC.Y3
49.

carbofuran

2-dimethylhen3-di hvdro-2,
2,
zofuran-7-91 methylcarbamate

50.

carbophe = nothion

A
I

S-J-chlorophcnylthiomethyl
dicthyl phosphorodithioate

51.

carboxin

5,6-dihydro-Z-methyl-l, 4-oxathi-invScarboxanilide

52.

cartap

S-2-dimethylaminotrimethylcnc
S,
his (thiocarbamate)

53.

chinomelhi = onate

A
F

6-methyl-l, Sdithiolo[4,
quinoxalin-2-one

54.

chloramben

II

S-amino-Z, 5-dichlorobenzolc acid

0 , O-

5-b]

_- /
3
SCH ,SP(OC,H& 2
(CH3),NCH(CH&ONHd2

/cc3

CO-OH

Cl

Cl
NH2

Table 1 ( Con~inrred )
Sl No.

(1)

Common Name

USC

(2)

(3)

Molecular Formula

Chemical Structure

Chemical Name
(4

55.

chlorbenside

+chlorobenzyl 4chloropkenyl
phide

56.

chlorMam (BIPC)

II

l-methylprop-2-ynyi 3-chlorocarhanilate

57.

chlordanc

1,2,&j, 6,7,8, S-octachloro-2,3,3a,

5, 7. ?a-hesahydro-4, 7-methanoindcne

chlorfenac

1-I

(2, 3,6-trichlorophenyl) acetic acid

59.

chlorfenson

l-chlorophenyl_I-chlc~robenzcne
phonate

60.

chlorfensul = phide

l-chlorophnzyl 2,-I, Qrichloro = bcnzenediazosulphidc

C,,N,,~CI,S
(6)

sul-

C,H,CI,

=suI-

Cl
/ \
u-

Cl
Cl

C,,lI,CI,NIS

61.

Chlorfelwinphm

2-chloro-l-(2, 4-dichlorophenyl) vinyl

diethyl

phosphitfe

CHCI
62.

chlorrnequat @ should be
P
stated which anion is present,
for example, chlornwquat chloride)

2-chloroethyltri methyl = ammonium

ion

ClC/+ CH2N+(CH3)3

,
63.

COOCH2-CH3
chlorobenzilate

ethyl 4, 4dichlorobenzilate

CKYe
AH

6<.

chloroneb

l,4dIcbloro-2,

65.

chloroph;l = cinone

2-[2?4-chlorophenyl)-2-phenyl=ace
tyll Mm-1, %lione

66.

chloropicrin

trichlorwritrornethane

5-dkrjeChoxybenzene

~!\
C-N02
~,/-

C5H,3CIN

Table 1( Continued )
St No.
(1)
67.

Common Name

Use

(2)

(3)

chlorothaldnil

Chemical Name

Molecular Formula

Chemical Structure

(6)

CgCl,N~

tetrachloruisophthalonitrile

CN

68.

chloroxuron

3-[4-(4-chlorophenoxy) phenyll-1, ldimethylurea

69.

chlorpropham

isopropyl 3-chlorophenylcarbamate

cl+

N-CO-N&H, )*

S
70.

chlorpyrifos

0, O-diethyl O-3, 5,6-trichloro-2pyridyl phosphorothioate

Cl

0;(OCH2CH &

Cl.

Cl
S

71.

Chlorpyrifos methyl

9, 0-dimethyl O-3, 5, 6-trichloro-2pyridyl phosphorothioate

Cl

08(0CH&

Cl

Cl

ClsHlsClN202

!-4

z*
fq,

EC

z .,

15

.,.

t+

C4

......

Table 1 ( Continued)
Common Name

Use

(1)

(2)

(3)

78.

coumaphos

SI No.

Molecular Formula

Chemical Structure

Chemical Name

(6)

(5)

(4)

O-3-chloro-4-methyl-2-oxo-2H-chr
o m e n 7-yl 0, 0-diethy) p h o r
phorothioate
CH3
.~

79.

coumatetralyl

4-hydroxy-3-(1, 2, 3, 4-tetrahydro-1-.
naphthyl) coumarin

80.

cyanazine

2-(4-chlorod-ethylamino-1,
azin-2-ylamino)-2methylpropionitrile

C19H1403

3, 5-&i-

tiH-CHp-CH3
81.

cycloate

S-ethyl N-cyclohexyl-N-ethyl(thiocarbamate)

C,,H,$OS
NCO-SCH2 -CH,
LH2 CH,

NH-CO-N(CH3j2
82.

Cycl uron

3-cyclooctyl-1, I-dimethylurea

C~lH$20

t;
00
%

..

83.

cyfluthrin

cyano-(4-fluoro-3-phenoxyphenyl)methyl-3- ( 2 , 2-dichloroethyl)-2, 2dimethyl-cyclopropane carboxylate

:;;

_I

D&&i lf

CH,

84.

Cyhalorhrin

(RS)-a&a-cyano-3-phenoxybenzyl(2)
-(IRS, 3RT)i2-Chloro-3i_~~~t~~:.
fluoropropenyl)-2,
cyclopropane = carboxylate

85.

cyhexa ti n

tticyclohexyltin hydroxide

86.

cymoxanil

1-(2-cyano-2-methoxyiminoacetyl)-3ethylurea

cypermethrin

(RS)-a&z-cyano-3-phenoxybenzyl( lR
S)-cb-truns-3-(2,2- dichlotovinyl)-2,
2-dimethylcycloptopanecatboxylatc

(23H,gClF3N03

c,/c=ctl

C19H3d)Sn

6H
CN
CH 3-CH2 - N H - C O - N H - C O - & N O C H 3

87.

cz:rO

CH,

CN

CF,

C7H,o%%

tf

Table 1 ( Continrted)
SI No.

Common Name

Use

(2)

(3)

(1)

Molecular Formula

Cheinical Structure

Chemical Name

(6)

(5)

(4)

--c-sCl

88.

2,4-D

(2,4-dichlocophenoxy)

acetic acid

Cl

89.

dalapon

2,2-dichloropropionic acid

/ \
- -

%H6C1203

OCH2-COOH

C3H4a202

O(CH &-COOH

90.

daminozide

CH3-y-COo#:

N-dimethylaminosuccinamic acid

WGV3

Cl

91.

dazomet

t e t r a h y d r o - 3 , Sdimethyl-1, 3, 5thiadiazine-Zthione

92.

2,4-DB

4-(2,4-dichlorophenoxy) butyric acid

93.

DBCP

1,2-dibromo-3chloropropane

94.

D-D mixture

mixture
of
1,
2Reaction
dichloropropane (see Sl No. 109) and
1, 3-dichloropropene (see SI No. 110)

(CH,),NNHCO-CH2CH&OOH

WloW2

c10bOa203

C3H5Br2CI

Br-CH2-CHBr-CH2CI

CICH &HCH 3
+

CH2 \c=c F CH2 \c=c /

H

(9

\C,

Cl

..

5;

95.

DDD

1, 1-dichloro-2, 2-bis (4-chlorohenyl)

ethane

CHCI,
96.

DDT

1, 1, 1-trichloro-2,
chIorophenyl)-ethane

2-bis

(4-

CI qH +u

CCI,
97.

delthamethrin

(S) - alpha-cyano-3-phenoxybenzyl
(lR)-ck-3-(2,2-dibromovinyl)-2,
dimethyl =cyclopropanecarboxylate 2-

98.

demeton-0

A
I

O,O-diethyl o-2-ethylthioethyl phos =

phorothioate

99.

demeton-O-methyl

A
I

0-2-ethylthioethyl 0 ,
phos = phorothioate

iir

(C,H, O),P-0-CH 2-Cb++-CH2-CH3

C,H ,903PSi

S
0-dimethyl

(w,O)2 !-O-CH2 -CH,-S-CH&CH,

100.

demeton-S

A
I

0, 0-diethyl S-2-ethylthioethyl phos =

phorothioate

101.

demeton-S-methyl

A
I

S-Zethylthioethyl 0, 0-dimethyl phos

= phorothioate

it
(C2H50)+-S-CH2-CH2-S-CH2-CH3

(CH3 O& P-S-CH, -CH2-S-CH2-CH3

(%H1903PS2

,-.

(1)

(3)

(4)

(5)

cH3y>yNHcH(cH)
102.

desmctryw

2-isf~prOpYhtmino-4-mcthylamino.~
-n_t{!th-ylth
if)- 1, ~, .fLtdazine

C&15N5S

NHCH3

CH3
103.

diazinon

A
I

1
\N

O, 0-diethyl O-2-isopropyl-&methyl
= pyrimidin-4-yl phnsphomthioate

CH(CH3)2
C12H21N20#S

Y
0:(OC2HJ2

s
N

104.

dibrommchlompmpnc

1, 2-dit)~]mf}-3-ehlorf>ptipane

8rCH2CHBt-CH2CI

/
(!X
COOH

10.5. dicarnba

3, 6-dichlom-o-atisic

acid

cl

0CH3

,,

106.

dichtobetil

2, 6dichlombnmnitilc

107.

dichlone

~, 3dichlom-1,

4-naphthoqtinonc

OH
I
108. dichkwophen

Ii
B

4, 4-dichlmn-2, 2
methyltxtediphcnol

I
cl

1(!9.

I. ?-dichlo

=mprqxdnc

110.

1, %-dio!)lu

rup:upcnc
i

111.

dichlorvos

2, 2-dichlorovinyl dimethyl ph~s~hiit~

cl
[:

5-dimethyl

PI

>

/\No
-

..
)

c1

.;:,.

l,$it:$,,!

!.CH30)2p-ocH=cci

-I
.,.

CH 3
CH s

. . . ..

-- .-. ...
; t,.], nwrl Nit IIW

il,i

1al)lt! I ( <:0)11;////(?(/ ,

...
IJsc

(2)

C!wtnimrl PfiIIUC

(3)

(4)

..

2,2. 2-trichloro-1, l-bis(cI

chlmophcnyl) ethanol

(~-z-dif.nt~thylalrba rr.wyl)-l.-mdhylv
inyl dirwthyl phwphak

,- .

,tlllcitfik

KIoIw-uIw

i<:
.

i 16.

.. ..
(hcwttu,

Formuln

(6)

(CH30)2P~,

(tHJ6NO#

,H
C=c

i .,
1:

117.

dit:ldrin

produci

contitining 85

percent

of

Ci2H8C160(IiEOD)

HEOI) (see fafer-)

118.

dimrochlor

perchloro-1, 1bicyclopcnta-2,
4-dicnyl

119.

dicthyl = Ioluarnidc

N, N-diethyl-m-toluarnidc

..
l.z
&

yl-i 2

-?
dirxr]tcrpbos

/d
\

CO- N(C2ii5)
I

CH3

C, ZH,7N0

0
LL

.-

lahle 1 ( Co,Uil?lrtri )
- SI IVI,.
,

; !t\

tommon Name

1 ke

..~,i~tl,.cl_;ri-~,i-.

Chemical Structure

themical Nanir

*.
_.
,,I.

::
3;

c4

i
:.-

dlmidaznn

(CH ,)2CHO-CO-0

2-see-butyl-4,6_dinitrophenyl
isopropyl carbnnate

An isomeric reaction mixture ot (1) 2.

6-dinitro-4-octylphenyl
crolonztcsand
4-dinitro-6-c,ccylphenyl
(if)
2.
crotonate\ NOTE - I he mixture normaliv contains bchvecri 4 and 5 parts
ofisbmen ol2.4-dlnitro-6octylphenyl
crotonates to Z 1l.1~ vf the 15omtrs ol
0 2N
2, 6-dinitro-l-oc:t\rll~tl~,~\,~ crotrinntv\

FH 3

O-CO-CH=CHCH,

I
CHdCH,),,CH(CH&,CH~
a
[Til

CH,(CH2),,CH(CHzjs_nCCi3
[n=O,l,Z]
04

1 2 9 . dinosauj

2-(1-methyIbutyl)-4,6dinitrophenol

O.,N
CHCH2CH2CH,
0 I
CHS

CH3
130.

dinoseb

C&uW~

2-see-butyl_4,6dinitrophenol

NO2
131.

dinoseb acetate

2-see-butyl-4,6dinitrophenyl acetalc

132.

dioxathion

S, S-(l, 4dioxane-2,3diyl) 0, 0, O,
O-tetraethyl bis(phosphorodithioate)

CH3CO-0

cH3
C,,NdW,

O2N

NO2
s

C,&,0&S4

Sb(OCHzCHa),
S;@CtizcH~ )2
S

133.

diphacinone

2-(diphenyIacetyI) indan-1,3-dione

c,,Pl@,

Table 1 ( Continued )
SI No.

Common Name

Use

(2)

(3)

(1)

134.

diphenamid

Chemical Name

Chemical Structure

(6)

(41

N,

Molecular Formula

Cl6Hl7NO

N-dimethyldiphenylactamide

bd2
135.

dipropetryn

2-ethylthio-4,6-bis (isopropylamino)1,3,5triazine

136.

diquat (it should be stated

which anion is present,
for instance diquat dibromide
or diquat dichloride)

9 , lo-dihydro-Sa, lOadiazoniaphenanthrene ion

2-(2,4dichlorophenoxy)
ethyl hydrogen sulphate

1 3 7 . disul

138.

disulfoton

0, 0-diethyl S-2-ethylthioethyl phosphorodithioate

%H:,N~S

C&$@@
0CH2CH20S0,0H

(C2H50),PSCH2CH2SCH2CH3

i3
%
(II
..

\
I/

(4

QQ

\
I/

-n

Jib

Table 1 ( Contimed)
SI No.

Common Name

Use

(2)

(3)

(1)

Chemical Name

Chemical Structure

(4

Molehuhr Formula

5)

Cl
145.

endosulfao

A
I

6,7,8, 9, lo-hexachloro-1,5,3a, 6,9,

9a-hexahydro-6, 9- methano-2, 4, 3benzodi-oxathiepin 3-oxide

J@

Cl

Cl
Cl

O$20

Cl

146.

endothalsodium

disodium 7-oxabicyclo [2. 2. l] heptane-2,3-dicarboxylate

COONa
COONa

147.

endrin

I
V

1, 2, 3, 4, 10, lo-hexachloro-6, 7epoxy-l, 4,4a, 5,6,7,8,8a-octahydroendo-1,4-exe-5,

S-dimethanonaphthalene

148.

EPN

O-ethyl 0-4-nitrophenyl phenylphos = .

phonothioate

149.

EPTC

S-ethyl dipropyl (thiocarbamate)

150.

erbon

242, 4, 5trichlorophenoxy)
2dichIoropropionate

ethyl-2,

_~~
[CHS(CH2),],NCO-SW2 CHs

0-CH2 -CH2-0-CO-Ccl2 -CH,

C,I-I,,NOS

C,,H9C&

1.51.

e~halfluralin

N-ethyl-N-(methylallvl)-2, 6-dinitro4-trifluoromethylaniline

HI
F

CH2 -C=CH2

CFs

CH2 CH,
0
152.

ethepon

CICHICHzk0H)2

2chloroethylphosphonic acid

8
[C, Hs 0) ,PS
153.

ethion

A
I

0, 0, 0; O-tetraethyl S, Smethylene-bis (phosphorodithioate)

2
$2 HI 0) 2Ps
!

154.

ethoprophos

O-ethyl S, S-dipropyl
phosphorodithioate

155.

etrimfos

0-6-ethoxy-2-ethylpyrimidin-4-yl
0-dimethyl phosphorothioate

156.

fenamiphos

ethvl, 3-methyl+(methylthio)-phenyl
isopropyl = phosphoramidate

0,

C,d-I,7W,PS

OiNHUi(CH;)
I
0CH2 CH.

C,,H,W,E
2

Table 1 ( Continued )
SI No.
(1)

157.

Common Name
(2)

fenarimol

Use
(3)

158. fenazaflor
P

4:

159.

fenchlorphos

(4)

(*)-2, 4-dichloro-alpha-(pyrimidin5-y]) benzhydryl alcohol

C,~H,ZCI~N,O

phenyl5,6-dichloro-2trifluoromethylbenzimidazole-l-car
boxylate

0, 0-dimethyl O-2,4,5trichlorophenyl phosphorothioate

0
160. fenfuram

ZE
Molecular Formula +.JI
..
&
(6)
E

Chemical Structure

Chemical Name

Cl

2-methyl-3-furanilide

(Y

Co-NH
161.

fenitrothion

0, Odimethyl O-4-nitro-m-tolyl phosphorothioate

162.

fenoprop

(T)-2-(2, 4, S-trichlorophenoxy)
propionic acid

C9H7Cl303

\
[

/
O
o

-n

s=.

..-

Table 1 ( Continued )
SI No;

Common Name

Use

(2)

(3)

(1)

169. fenuron

Chemical Name

Molecular Formula

Chemical Structure

(5)

(4)

NH.CO.N(CH&

l, l-dimethyl-3-phenylurea

/0\
Cl

170.

fenvalerate

(RS )-alpkr-cyano-3-phenoxybenxyi(RS )-2-(4-chlorophenyl)-3-methylbutyrate

(CH & CH.CH.CO.OdH

-+
171.

ferbam

iron tris (dimethyldithiocarbamate)

[(cH~& NCSS-1 5 3

172.

fluazifop

(RS)-2-[4-(5trifluoromethyl-2pytidy
loxy) phenoxy] propionic acid

CF,o 0 0 O:;iO.OH
NO2

173.

fluchloralin

N-(2-chloroethyl)-aI@m, alpha
alpha-trifluoro-2,6-dinitro-N- propyiP-toluidine

cF3

N/CH2cH2C

\ (CH 2)2W

GNO2

174.

flucythrinate

(RS)-alpha-cyano-3-phenoxybenzyl(S)
-2-(4-difluoromethoxyphenyl)- 3
methybutyrate

175.

fluometuron

1, 1-dimethyl-3-(alpha, alpha, alphatrifluoro-m-tolyl) urea

NH.CO.N(CH 3 jz

GhVW

CF3
176.

fluvalinate

177.

fonofos

178. formothion

O-ethyl S-phenyl (RS)-ethyl phosphonddithibate

~1&50ps2

S-(N-formyl-N-metS.ylcarbamoylmetfiyl)
-0, O-dimethyl phosphorodithioate

C&NWS,
0

il

179.

fosetyl

ethyl hydrogen phosphonate

CH2CH30ToH

c2H@3p

Sl No.
(1)

Common Name

Use

(2)

(3)

Chemical Name

Molecular Formula F

Chemical Structure

(4)

CH3 CH3
I
I
?.CO.N-S-NCO.O(CH 2)3CH3

180.

Furathiocarb

butvl 2,3-dihydro-2, 2-dimclhylbcnzofkran-7-yl N , N-dimethyl-N. Ndithiocarbamate

ox
<I0

181.

furrnecyclox

methyl N-cyclohexyl-2, 5-dimcrhylfuran-3-carbohydroxamate

182.

gamma-HCH or gamn~a-BHC

(1, 2, 4,5/3,6)-l, 2, 3, 4, 5,6-hexa =

chlorocyclohexane

!li

CH3

Cl

CH3

Cl
/OH

183.

gibberellic acid

(3S, 3aS, 4S,4aS,7S,9aR, 9bR, lZS)7,12-dihydtoxy-3-methyl&

methylene-2_oxoperhydnMa,
7-methano-9b, 3-pmpeno- [ 1,
3-bifuran-4] carboxylic acid
-.

pJ-g
CH2

.O
184.

glufosinate

LX-homoalanin-Cyl (methyl) phosphinic acid

CH3,!CH 2CH CHCO

2,
.Ot
6H

i4H2

W 12NW

185.

glyodin

2-heptadecyl -2-imidazoiine acetate

C&(cH

NH

2) ,5 -CH3,CH3-COOH

I
N

(Y

o
186.

glyphosate

N-(phosphonomethyl)glycine

H0.COCH2NHCH2!(OH)2

o
187.

glyphosine

N, i?-bis (phosphosmethyl)

18ti.

gwtzatine

1,1 -iminodi (octamethylene)

HO. COCH2 N[cH$(oH)-2]

gl ycine

NH
II
NH2 CNH(CH fla NH(CH2)aNHCNH z
~H

diguanidine

-.
w

cl

189.

HCH or BHC

Mixed isomers of 1,2,3,4,5,

chlomcydohexane

c1

6-hexa-

c!

cl
:+.

cfjH&l~

c1

cl
cl

190.

H~OD

(IR,4S, 40LY,3R,6R, 7S, &S, 8uR)-1, 2,

3,4, 10, Whexachloro-1, 4, 4a, 5.6,

7,8, 8a-odahy&o-6, 7-epoxy-1.4, 5,

8- dirnetharmraphlhakme

cl
cl

c1
cl

o
&

c1

c&cl&r

Table 1 ( Confinued
Common Name

S1 No.

Use

~hcmkal Name

)
Chemical Structure

Molecular

Formula

(1)

(2)

(3)

(4)

(5)

(6)

cl

c1

c1
191.

h@ach]or

1,4,5,6,
7,8, fi-heptachloro-la, 4.7,
7a-!etrrrh@[u-4,7.. methfinoindene

cl
192.

hCXWhlOrohenzene

hexachlcumhenzene

I
@

c1
c1

cl

c1

/-

cl
u
m
193.

hexrzinone

M:yk)l]cxyl-rj.di methy+rminn-1-met

hyl-1, 3, 5-trinzine-2, 4 (Ilf, 3H)-dionc

cl

-%

I
c,

CH3)2NW
C12H20N402

Nf4

l-f
Q

194.

195.

HHDN

IM

0:

1,2,3,4.10, 10-hexiictrlofo-1, 4, &$,

8: fla-hexahydm-tio-l,
4-errdo.5, fJdrmethano-naphtalenc
.

indol-3-ylac@ic acjd

C12H8C[6
.

N.=

(l-J/

CHCO.OH,

C10H9NC)2

196. IBA

4-indol-3-ylbuttyric acid

197.

S-benzyl 0, 0-diethyl
phosphorothioate

IBP

198.

ioxynil

4-hydroxy-3, S-di-iodobenzonitrile

Cl
199. iprodione

rt;

3-(3, Sdichiorophenyl)-Nisopropyl2,4-dioxoimidaaolidine-lcarboxamide

Cl

/D-\

CO.NHCH(CH&

w3)2CH\N_
200. isazofos

O-khloro-I-isopropyl-W-1, 2, 4-triOdiethyl
phosazol-3-yl 0 ,
phorothioate

C7H&NO

OH

N.

aANA &(OC2H5) 2

Cl

Cl

S
Cl

201. isobenzan

1,3,4,.5,6,7,8, ILoctachioro-1,3,3a,
4,7,7a-hexahydro-4,7
methanoisobenzofuran

Cl

'Cl

Cl

Cl

(-%H9Ci20

E
z
Molecular Formula (n
..

Table 1 ( Contimed)
S1 No.
(1)
202.

203.

Common Name

IJse

(2)

(3)

isofenphos

isonorunon

II

Chemical Structure

Chemical Name

(6)

(5)

(4

CdbW,~

O-2-isopropoxycarh~l~~ lO-ethyl
phosisopropyl
phenyl
phoramidothioate

07CH*CH3
NHCH(CH &

, NH-CO-N(CH &

A mixture of the two isomers: 1, Idimethyl-3-(perhydro4,7- methano =

inden-1-yl) urea and l, l-dimethyl-3(perhydro-4,7- methano = inden-2-yl)
urea

/0

Cdb,W

?CO.NHCH 3

204.

isoprocarb

I-isopropylphenyl methylcarbamate

2 0 5 . isaprothiolane

di-isopropyl 1,
ylidenemalonate

206.

3-(4-isopropylphenyl)-1,
urea

isoproturon

CWH,) *

%H,W,

3dithiolan-2-

ldimethyl

NH.cO.N(cH,),

C12HlSNZO

207.

kasugamyoin

1 L - 1,3,4&S, 6-l-deoxy--2,3,4,5,
6- penta =
hydroxycyclohexyl-2-amino-2,3,4,6
- tetra =
d e o x y -4- ( a!pho - iminoglycirio) U&I -D- arabino- hexopyranoside

C14HAW9

I!%.

kinoprcne

prop-2-ynyl (1) - (E, E) -3, 7, 11 trimethyldodeca- 2,4-dienoate

(C,),CC,C,C

C, ,I 12&O,

2CHCT

H c=c$=c<Io .OC C C
2 C,
H
A
g

209.

lenacil

3-cyclohexyl-l,S, 6,7tetmhydroxyclo = pen tapyrimidine-2,

4 (33 - dione

.- \
I

0
Y
N

Qrf
0
0

210.

leptophos

O-4-bromo-2, S-dichlorophenyl
methyl phenylphosphonothioate

211.

lindane

Product containing not less than 99

percent of gamma - HCH or gamma BHC (see SI no. 182).

212.

linuron

3-(3,4-dichlorophenyl) -l-methoxy-lmethylurea

O-

Cl

C, ,l-l,sN202

Table 1 ( Continued )

St No.

Common Name

Use

(2)

(3)

(1)

213.

malathinon

Chemical Name

Chemical Structure

S-l, 2-bis (ethoxycarbonyl)ethyIO,Odimethyl phosphorodithioate

(6)

(5)

(9

%
Molecular Formula (h
..

CH2C0.COC2H5

(CH &CH (

%1~1904f%

C0.0C2HS

214.

maleic hydrazide

1,2-dihydropyridazine-3,6dione

C4H4N,02

215.

mancozeb

manganese ethylenebis (dithiocarbamate) (polymeric) complex \vith

zinc salt [complex of zinc and maneb
containing 20 percent of manganese
and 2.5 percent of zinc. It should he
stated which salt is present, for example, mancozeb chloride] (Chemical
structure is fully not known)

[C,HeMnN&]*
(ZN)

216.

mancb

manganese ethylenebis (di thiocarbamate) (polymeric) [chemical structure of the product is not yet fully
known]

217.

mazidox

tetramethylazidophosphonic diamide

W3W\ 4 0

C,H&OP
(CHS)~N/ , Ns

218.

MCPA

4-chloro-0-tolyloxyacetic acid

219.

MCPEi

4-(4-chloro-0-tolyloxy) butyric acid

220.

mecarbam

A
I

S-(N-ethoxycarbonyl-Wmethylcarb
amoyl = methyl) 0, O-diethyl phosphorodithioate

2 2 1 . mecoprop

(*)-2-(4-chIoro-O-tolyluxy) propionic
acid

C,H&Q

C,,H13C03

-CH3
I
CzH50.CO.NCO.C 2SP(OC2 5)2
# Cl&,lC~O3
.

Cl
\

222.

MEMC

2-methoxyethylmercury chloride

A
I

S-4, 6-diamino-1, 3, 5triazin-2-yl =

methyl 0, 0-dimethyl phosphor0 =

CH ,O-(CH 2) ,-HgCI

C3H7ClHg0

S
223.

menazon

H2Ny NY CH,S&OCH,),

WWW2%

dithioate

224.

mephosfolan

diethylj-methyl-l, 3-dithiolan-2-yli =
denephosphoramidate

C8H16N03PS2

Table 1 ( Continued )
SI No. Common Name
(1)
225.

(2)

Metalaxyl

2 2 6 . metaldehyde

USC

M o l e c u l a r Formula E

Chemical Structure

Chemical Name

(3)

methyl N-(2-methoxyacetyl) -N-(2,6xylyl) - LX-alaninate

r-2, c-4, c-6, c-8-tetramethyl -1, 3, 5,

7-tetraoxocane

227.

metam sodium

sodium methyldithiocarbamate

228.

methabenzth= iazuron

1-benzothiazol-2-yl-1,3-dimethylurea

229.

methacrifos

O,O-dimethyl (E)-0-2-methoxycarbonylprop-l-enyl phosphorothioate

CSH1604

CH3-N-Na=CS-SH

C2H4NNaS2

C7H13WS

(CH3wO;\C=C,cH3
d
I

0, S-dimethyl phosphoramidothin:rrt

I
I
CH30PSCH 3
I
NH2

H/

CO.OCH,
C2H9N0,PS

231.

methidathion

S-2, 3-dihydro-5-methoxy-2oxo-1, 3,
4-thiadiazol-3-ylmethl 0, 0-dimethyl
phosphorodithioate

CH30XS~:H2S~(OC,),
NCH3S

232.

methomyl

233.

methoprene

234.

methoxychlor

S-methyl N-(methylcarbamoyloxy) =
thioacetamidate

C=N-OCO.NHCH3

CHs /

isopropyl F-E) - W9 -ll-methox~-3~

7,11-trimethyldodeca-2,4- dienoatq

1, 1, 1-trichloro-2, 2-bis (4-methoxy- - c+=& f 0 OCH;

phenyl) ethane
CCI

.235.

zinc ammoniate ethylenebis

(dithiocarbamate) - poly [ethylenebis
(thiuram disulphide)]

metiram

236. metobromuron

3-(Cbromophenyl) -l-method
1-methylurea

W15Wh

3
Not oken
r

[(-S.CS.NH.CHzCH2NH.CS.S-)--ih(NH3~~,
(-S.CS.NH.CH2CH2NH.CS.S-)
[
,

Table 1 ( Continued )
SI No.
(1)
237.

Common Name

Use

(2)

(3)

metolachlor

238. metoxuron

Chemical Name

(4)

2~~oro-6ethyl-~~2-methoxy-l-met
hyl = ethyl) acet -0-toluidide

3-(3-chloro-4-methoxyphenyl) -1, Idimethylurea

(6)

(3

C1+I,,CIW,

NH.C0.N(CH3),

N
239.

metribuzin

4-amino 6-tert-butyld, 5-dihydro-3methylthio-1,2,4-triazin-5- one

2-methoxycarbonyl-1-methylvinyl
dimethyl phosphate (It should be stated
which isomer is present, for example,
trun.s-mevinphos)

Molecular Formula

Chemical Structure

0
240.

mevinphos

C,H,,OQ

(CH30)2!OC=CH.C0.0CH~
bH3

t;
g
VI
..

5
z

241.

mesacarbamale

I-dimcthylamino-3, 5-xylyl methylcarbamate

242.

molinate

S-ethyl N, N-hexamethylenethiocrbamate

353.

monocrotophos

dimethyl (E)-1-methyl-2-(methylcarbamoyl) vinly phosphate

NC0.SC2H5

II

(CH30)2po\

C,H,,NOS

c,H14N05P
,H

CH 3/c=c\C0.NHCH3

244.

monolinuron

3-(4-chlorophenyl)-1-methoxy-l-me
thylurea

245.

monuron

3-(4-chlorophenyl)-1, 1-dimethylurea

216.

MSh4A

methylarsonic acid

nabam

disodium
bama te)

317.

ethylenebis (dithiocar-

C,H,,ClN,O,

cl

----($-

NH.CO.N(CH~)~

CH, - N H - C S - S N a
I
CH2-NH-CS-SNq

C9H11CN20

C&N2N&

t3

Table 1 ( Continued )
51 No.

Common Name

(1

(2)

IJse

(6)

(5)

(4)

(3)

Molecular Formula

Chemical Structure

Chemical Name

?I

_-is.

naled

BrCI,CCHOP(OCH,)i

1,2-dibromo-2,2-dichloroethyl
dimethyl phosphate

Qr
~H2m60.0H

3JY.

a@o-naph-thaleneaceti~ acid

250.

naptalam

251.

neburon

2-( 1 -naphthyl)

C12H1002

acetic acid

C1sHnN03

N-1-naphthylphthlamic acid

l-butyl-3-(3,4-dichlorophenyl)1-methylurea

a.-&

YH3

NH.CO.N(CH& CH,

Cl

OH
252.

niclosamide

5-chloro-N-(2-chloro-4-nitrophenyl) =
salicylamide

02NeNH-! Q
\

Cl

Cl

E
WI

..

5;
if

253

nilrolerr

2, 4-dicMompbenyl
ether

4-nitnrphcnyl
.
.

c1
254.

noruron

255.

(ml(!lhoal(!

7.56.

oxatjazon

1,
l-dimcthyl-3-(perhydro-4,
rnclhano = indcn-5-yl) urea

7-

0,
O-dimethyl
S-rr]ethylwbarnoylethyl phosphorothioa!c

II

(CH3)3L

C13H22N20

c&f3NHco.(342sp(0(3+

(Y
NN

0CH(CH3)

\/.

C+ ~2N0415

3)2,
;

C15H19C12N@3

.o-

&.
d

cl
2.57.

exam yl

N, Ndmtbyl-2-metifi6timoylo~.
. imirto-2-(rnethyithio) +wktamide
.

2-hydroxethyldirrrethylammoniurn
6&hydr0-@o&l,

(CH3)2NW.C=N0.C0.

NHCH3.

C7H13N303S

!CH s

5-

NH+-COOH.(CFQ

phU@pyTidaZin-4-yloxamate
of~

~~
O*

Ji4

t4HC0.N(CH3)2

N-CH2 CH2UH
CHBrTv

S1 N(I.

(1)

{;olimlon Nnme

Use

Chemicrd Name

(q

(3)

[4)

oxine-qper

260.

exintKu

ox ywrboxin

],

bis (quirroli n-t+ oh[o) copper or cupric

tkpinolimxide

5, 6dlhydrrK2-melhyl-1, 4-oxathi-in3-carboxanilide 4. 4dloxide

A
[

S-2-ethylsulphinylelhyl O, O-dime =
thyl phosplrorilthioste

oriydemetrm meUryl

Molecular Formuln

C%emitad Structure

(6)

Clotl#uN202

-:
261.

m
Qe

Table 1 ( Conthwd )

fi

(CH30)2PSCH2CH2

C6H],504PS~

SC2HS
/ O-CH ~-CH3

262.

ox ylkrorfcn

2-chioru-alfia, alpha, alpha, -@ifluoro-p-tolyl-3-ethoxy-4- nitrophenjt

ether

F3C

-cya-,
cl

fJ

C15111
@5N04

.,m

263.

l, l-dimethyl-4,4-bipyridinium
paraquat
H
[It should be stated
which anion is presenb for instance, paraquat dichloride or paraquat bis (methyl sulphate)]

264. parathion

A
I

0, 0-diethyl 0-4-nitrophenyl phosphorothioate

Cl&l4N%~

265.

A
I

0, 0-dimethyl 0-4-nitrophenyl phosphorothioate

C9H,,-,N05PS

II

.v-propyl butyl (ettiyl) thiocarbamate

parathion methyl

CH3(CH2)3-IC0.SCH pCp H,
2 6 6 . pehulate

C,o%WS
C2H,

267.

pendimethalin

N-l (l-ethylpropyl)-2, 6-dinitro-3, 4xylidine

268.

permethrin

3-phenoxybenzyl (IRS)-&s-from-!( 2 , 2-dichlorovmyl)-2, 2- dimethylcyclopropanecarboxylate

tl

E..
5
P

S1No.

Common Name

use

(2)

(3)

(1)

Molecular Fonda

Chemical Structure

Chemical Name

(6)

(5)

(4)

5
%
~
..

G
x

269.

3-phenoxyhenzyl

phenothnn

c:Jt~~o~

(UK-)-ciWwr.\-

Chrysanthernate

$
270,

phenthoate

A
I

VI
9

271.

phorate

/O
\

(CH30)2 PS:H.C0.0C2H5

ethyl 2-dimethoxythiophosphorylihios-iJlpilli2-phenylacetate
or
cthoxycsrbonylberizyl 0, CJ-dimcthyl
phosphoroc!ithioate
0, O-diethyl S-ethylthiomethyl
phorodhhioate

C1lH170.iPs~

phos-

C7HI ~02PS2

(C2tiS0)2f%CH2SC2H5

272.

phosdone

3-dihydm-2~xobenz =
oxazol-3-ylglelhyl 0, 0- dieth yl phos phomcthhioate

S-6-chloro-2,,

00

c1

cl/

o
phosmet

Odimethyl S-phthalimidomeihyl
phosphorodithioate
,
O,

\
a

b-..
)

IY

273.

C12H15CIN04PS2

N CH2SP(OC2H5)2

s
II

N-cH#w3cH3)~

6\/

A,

--,

. . ._..,____

,,, !.! -w

tl

Table 1 ( Continued )
SI No.

Common Name

Use

(2)

(3)

(1)
279.

pindone

2 8 0 . piperonyl butoxide

Chemical Name

Molecular Formula

themical Structure

(4)

(6)

(5)
0

I-pivaloylindan-1, 3-dione

2-Pbutoxyethoxy) ethyl ~-P~OPY~ = CH,(CH~)~OCH+H,OCH, CH,OCH,

CO.C(CH &

piperonyl ether

CHdCHdz
281. piperophos

S-2-methylpiperidinocarbonylmethyl
0, 0-dipropyl phosphorodithioate

I:

N-CO.CH ,SP(OCH 2CH2CH 3)2

c

CH,

282. pirimiphos methyl

A
I
N

0-2-diethylamino-6-methylpyrimidi
0-dimethyl
phosn-4-yl-0,
phorothioate

283. pretilachlor

2chloro-2, 6-diethyl-N-(2-propoxy
= ethyl) acetanilide

C 2H5

C14H1403

8
..
F

284.

prochlcmw

:)*CH3
c/\

l-fWpropyl-iV-[2-( 2,4,6 -trichloKI

=
phenoxy) cthvl~ carbamoylirnidazolc

y0,NCH2CH Zo
N
285.

04-bmmo-2+tiflrophenyl

O-e(hylS-

propyl phosphorothioale

e,

286.

prometiync

2, Mis

(isopropylamino) -6-methylthio-1, 3, Mriazinc

-Pc,

c1

I
L>
profenofos

c@l@3N30~

Q
/

o!-OCZHS
kCH2C2H3
cl
NHCH(Cti&

CH3S

c~(,H19N5s

K.
Y%
N/
f

iJHCH(CH3)2
287.

propanil

(:J-l@7N0

3, ~dichkJropKipiOnSnilidc
c,/\

u
w

NH.C0.CH2CH3

f(CH3)3

Q
/

288.

propargite

2-(4-tert-butylphenoxy)
prry+myl Sulphk?

+30hexyl

OSO.0CH2C5CH

cl

C~91_lZ40@

Table 1 ( Continued )
Sl No.

Common Name

Use

(2)

(3)

(1)

Chemical Name

(4)

Chemical Structure

(5)

Molecular Formula

#
z
..

(6)

8
289. propetamphos

isopropyl (3-[ethylamino(methoxy) =
phosphinothioyloxy] isocrotonate

290.

propham

isopropyl carbanilate or isopropyl

phenylcarbamate

291.

propiconazole

(A)-l-[2-(2,4-dichlorophenyl)-4-pro
pyl-1,3-dioxolan-2- ylmethyll-l-H-1,
2,4-triazole

CH3CHzNHPO\

, H
c=c
CWCH/
CO.OCH(CH&
3
NH.CO.OCH(CH&

C,ob0N04PS

C,&dO2

CH, (CH 2)2

CH3
292.

propineb

polymeric zinc propylenebis

(dithiocarbamate)

293.

propoxur

2-isopropoxyphenyl methylcarbamate

294.

propyzamide

3,5-dichloro-N-( 1,l
dimethylpropynyl) = benzamide

[-S.CS.NHCH2CHNHCS.S.Znw] x
O.CO.NHCH 3

O.CH(CH 3)2

(C5H&%Znh

295.

prothoate

A .

0 , O-diethyl S-isopropylcarbamoylmethyl phosphorodithioate

C,H,,NO&

(c3),CNco.c,s~(*c~~)~
CH3
,

296.

prynachlor

2-chloro-N
acetanilide

C,,H,,CINO

(1-methylprop-2-ynyi)

297.

pyracarbolid

3, 4-dihydrod-methyl-2ff-pyran-jcarboxanilide

298.

pyrazon (chloridazon)

5-amino-4-chloro-2-phenylpyridazin
-3
(2-)-one

N\CO_CH 2 Cl

CH3 CH20.C0
299.

pyrazophos

AH-C-CH

ethyl 2diethoxythiophosphorylo~~ - j
methyl = pyrazolo [l, S-a] pyrimldme6-carboxylate

CH3

St No.
(1)
300.

Common Name

1Jse

(2)

(3)

Chemical Name

Chemical Structure

(9
cinerin I-(lS)-3-[(Z)-bul-2-enyl]-2methyl-4-oxocyclopent-2-enyl (lRjtrans-chrysanthemate

pyrethrins (the term is used

collectively for 6 insecticidal
constituents, cinerin I, cinerin II,
jasmolin I, jasmolin II,
pyrethrin I, and
pyrethrin II

cinerln II - (lS)-3-[(Z)-but-2-enyl]-2methyl-4-oxocyclopent-2- enyl (lR)trans-3-i(E)-2-methoxycarbonylprop

-1 enyl]-2,2dimethylcyclopropanecarboxylate
jasmolin I- (lS)-2-methyl-4-oxo-3[(Z)-pent-2-enyl] cyclopent- 2-enyl
(lR)-rruns-chrysanthemate
jasmolin II-(CT)-2-methyl-4-oxo-3[(Z)-pent-2enyl) cyclopent-2- e n y l
(lR)-lrunsd-[Q-2methoxycarbonyl
prop-l-enyll-2,
2- dimethylcyclopropanecarboxylate
pyrethrin I- (PC)-2-methyl-4-0x0-3[(.Z)-penta-2, 4dienyl] cyclopent-2enyl (lR)-trans-chrysanthemate

301. pyrinuron

pyrethrin II-(2-methyl-loxo-3[(z)-penta-2, 4dienyl] cyclopent-2enyl

(JR)-truns-3-[(E)-2-methoxycarbonyl
prop-I-enyl]- 2,
2dimethylcyclopropanecarboxylate
l-(4-nitrophenyl)-3-(3-pyridylmethyl)
urea

Cl-l2 NH-CO-NH

Molecular Formula

fz

Ii

fi-chl oro-3-phcl]~lpy ridazil]-4-yl

octyl Ilrioca rhona [C

cl

.$-

Clul [2f(:lN

,K

b
il

CH3(CH2)7
I

(), O-die[hvl O-auirmxdin-2-yl

phorolhimk

ph{N-

Scoo

\
/
C121115N203PS

.()-s
.-

O@CH2CH3)2

o
N02

yu.

quintmcne (1CNSJ

c1

-J

305.

rcwtcthrin

fRS~-ci\-

C(,CIJQ

c1
u,

cl

c1

cl
( .

.il..,,~l

(CH3)2C=CH
.H~c00cH2
CH3

~
o
c

CH s
/

&=CHZ

H
t

0--%-

..

CH30
6CH3

--3
i

Table I ( Confinrrd )
Sl

No.

Common Name

1 se

Chemical Name

Chcmiml Structure

Molecular

Formula

E
P
..

(1

121

3)

OH

309.

sethoxydim

OCH 2CH3

(*)-24 I-ethoxyiminobutyl)-5-[2-(et
hylthio) =
propyI]-3- hydroxycyclohex-2 enom

!J

&CH,),CH,
CH3
I CH3 CH ,&HCH,

310.

simazine

2-chloro-4, 6-bis (ethylamino)-1,3,5triazine

CpHSNH

OH
y,;-(

C7H12CINS

\
N
r

NHC2H5

311.

sirmate (dichloromale)

Ii

3, 4-dichlorobenzyl methyl carbamatc

312.

strychnine

strichnidin-IO-one

313.

sul fometuron

2-[3-(4, 6-dimethylpyrimidin-2-)I)
urei = dosulphonyl] benzoic acid

CH3 NH.CO.OCH 2

C-3

Table 1 ( Conlinueri )
S1No.

Common Name

[kc

(q

(3)

(1)

Chmnical Name

Molccul;w FormuliI

Chemical Struclure
i:

(4)

(6)

Ss
314

Sullr)kp

,4

0,0,0,0
-tcm]clhyl
dithiopyrnphospha[c

315.

sulphnxiclc

l-nlcthyl-2<3,4 -mcthylcncdit>x? }jt]l.

nyi) ~thyl octyl mlphbxidr

316.

SU@phOS

O-ethyl
pruplyl

()-4 -meth!llhio@cnyl

(C2H50)2kk*2Hd2

CH2 CHMe.SO(CH2)7Me

~;--.~

>

i
:~H,s

/\

phosphomdiihinate

CJ,JI@$

~H2C2%

0C2H5

-c)-

cl
317.

2.4, 5--r

C9H5C1303

(2, 4 Mrichkmrpherroxy) arxtic acid

~,
,

i
t~

~~,~~

cl

318.

r(x (S(dhJti dt)

sodium Iridrloroacelate

c13C.C0.0-Na+

. (j

31Y.

320.

tebuthiuron

tecnazene

321. temephos

l-(5tert-butyl-1,3,4-thiadiazol-2-yl)1,3dimethylurea

1,2,4,5-tetrachloro-3-nitrobenzene

U,O,O,O-tetramethyl 0 , O-thiodip-phenylene his (phosphorothioate)

CyH16N,0S
(CH3)3C y Sk ~~.NHCH3

C,HCI,N02

(C, O$)&_ S 0 o,~,l%,,,r,.~

322.

TEPP

tetraethyl pyrophosphate

C&oO,f2

323.

terbacil

3-reti-butyl-khlorod-methyluracil

CyH,,CIN,O,
0
NHC(CH 3j3

324.

terbuthyl = azine

2-rert-butylamino-4-chlorod-ethylami
no-l, 3,5,-triazine

CyH,,CIN5

NHCzH5

t;

.E.
5

Table 1 ( Continued )
Sl No.

(1)

Common Name

Use

Chemical Structure

Chemical Name

(6)

(3

(2)

Molecular Formula

@HsS y N y NHC(CH3)3,

N
32.5.

terbutryne

2-krt-butylamino-4-ethylamino-6-m
ethylthio-1,3, S-triazine

AN
C,oH,,W

NHC~H~

326.

tetrachlor = vinphos

(Z)-2-chloro-1-(2,4,5-trichlorophenyl)
= vinyl diiethyl phosphate

Cl

327.

tetradifon

-I-chlorophenyl 2 4 S-trichlorophenyl
sulfone

Cl

328.

tetramethrin

3,4, 5,6-tetrahydrophthalimidomethyl
(IRS)-cis-trans- chrysanthemate

-a/

Cl

Fi
E

(II
..
b

329.

thiabendazole

330. thiobencarb

2-(thiazol-4-yl) bcnzimidazole

f-1

S-4-chlorobenzyl d i e t h y l (thiocarbamate)

331.

thiocyclam

332.

thiometon

A
I

S-2ethyhhioethyl0, Odimethyl phos phorodithioate

333.

thionazin

I
N

O,O-diethyl 0-pyrazin-2-yl phosphorothioate

.I

N, A-dimethyl-1,
ylamine

2 ,

~,&7N3S

3-trithian-5-

G%W3

S
II
(CSO),PS(C~,SC~S

S
-?

O!(OC,H,),
NHCS.NHCO.OCHS

334.

thiophanate methyl

dimethyl 4, 4-(0-phenylene) bis (3thioallophanate)

NHCS.i4HC0.0CHI

335.

thiram

bis (dimethylthiocarbamoyl) disulphide or tetramethylthiuram disulphide

(CH,),NCS.S
I
(cH~)~NCS.S

C,H,&S,

Table 1 ( Continued )
SI No.

Common Name

IJse

(2)

(3)

(1)

336.

tolclofosmethyl

Chemical Structure

Chemical Name

2,6,dichloro-I?-tolyl
phosphorothioate

O,O-dimethyl

CHS

O$OCH&

A reaction mixture of chlorinated camphenes containing 67 to 69 percent

chlorine

triadimefon

1-(4-chlorophenoxy)-3,3dimethyl-l(lif-I, 2,4-triazol-1-yl) butanone

triadimenol

l-(4chlorophenoxy)-3,3dimethyl-l(UT-1,2,4-triazol-l-yl) butan-2-01; it is
a mixture of 2 diastereoisomeric forma

Cl

[(CH3) CH& NC0.SCH,k=CC12

337.

toxaphene

338.

339.

Molecular Formula

340.

tri-allate

1-I

S, 2, 3, 3-trichloroallyl di-isopropyl
(thiocarbamate)

341.

triazophos

0, 0-diethyl 0-1-phenyl-W-1, 2, 4triazol-3-yl phosphorothioate

STRUCTURE UNKNOWN

CtdI,nCI, (approx)

OH
I.
0-CH-CH.C(CH&
I
N\
/
d-!!f
C&,&I,NOS

t:OP(OC.H,),
II

iz

..

342.

Tributyl phosphorotrithioite

tributyl phosphorotrithioite

343.

trichlorphon

2-trichloro-ldimethyl
2,
2,
hydroxyethylphosphonate

Cl3 CCHP(OCH&
I

344.

triclopyr

II

3 , 5 , 6-trichloro-2-pyridyloxyacetic
acid

Cl

345.

tricyclazole

S-methyl-l, 2,4-triazolo [3, 4- b] benzothiazole

C12H27PS,

I:

C,H&I,O,P

OCH,CO.OH

C,H&S

346.

tridemorph

2,6, dimethyl-4-tridecylmorpholine

347.

trifluralin

2, Gdinitro-N, N-dipropyl-4-trifluoro=
methylaniline

cu_

/-(

CHS -(CH 2), 2 - N,

C,,H,,F&O,

Cl, CFHNQCHO

triforine

1 , 4 - b i s ( 2 , 2 , 2-trichloro-l-formamidoethyl) = piperazine

0
/

2-CH 2-CH,)2

348.

CH3

0
N

CI,CCHNHCHO

t;

Table 1 ( Concluded )
SI No.
(1)
349.

Common Name

Use

(2)

(3)

validamycin

Chemical Name

Molecular Formula

Chemical Structure

(5)

(4)

OH

&(I, 3, 4/2, 6)-2, 3dihydroxy-6hydroxymethyl-4-[(lS, 4R, 5% 69 -6

5, 6-trihydroxy-3-hydroxy=methylcyclohexyl
cyclohex-2-enylamino]
beta-D-glucopyranoside

HO

OH

0-dimethyl S-2-(l-methylcarphosethyl
bamoylethylthio)
phorothioate

vernolate

S-propyl dipropylthiocarbamate

vinclozolin

3 - ( 3 , 5dichlorophenyl)~S-methyl-5
vinyl-l, 3-oxazolidine-2,4- dione

350.

vamidothion

351.

35.
i

0,

CH3
I
CH3NHC0.CHSCH 2CH 2SP(OCH 3)2

..

353.

warfarin

4-hydroxy-3-(3-oxo-1-phenylbutyl)
coumarin

354.

zineb

Zinc ethylenebis (dithiocarbamate)

(polymeric) (the chemical structure is
not yet fully known)

355.

Gram

zinc bis (dimethyldithiocarbamate)

C19H1604

.E.
tx

IS 885 : 1994

ANNEX A
( Clause 5.2 )
PESTICIDES NOT REQUIRING COMMON NAMES
Sl

No.

Sf
No.

Name ofpesticide

Name of Pesticide

1. Aluminium phosphide

28. Ethyl mercury phosphate

2. Ammonium sulphamate

29. Ethylene dibromide

3. Barium carbonate

30; Ethylene dichloride

4. Barium fluorosilicate

3 1. Hydrogen cyanide

5. Barium polysulphide

32. Hydrogen phosphide

6. Boric acid

33. Lead arsenate

7. Cadmium based compounds

34. Lime sulphur

8. Calcium arsenate

35. Magnesium phosphide

9. Calcium cyanide

36. Mercuric chloride

10. Carbon disulphide

37. Methyl bromide

11. Carbon tatrachloride

38. Methyl mercury chloride

12. Copper acetoarsenite (Paris Green)

39. Methylene chloride

13. Copper arsenate

40. Nickel chloride

14. Copper cyanide

41. Nicotine. sulphate

15. Copper hydroxide

42. Pentachlorophenol

16. Copper naphthanate

43. Phenyl mercury acetate

17. Copper oxychloride

44. Phenyl mercury chloride

18. Copper sulphate

4.5. Phenyl mercury salicylate

19. Cuprous oxide

46. Phenyl mercury urea

20. y-dichlorobenzene

47. Phosphorus paste

21. Dusting sulphur

48. Potassium cyanide

22. EDCT mixture

49. Sodium cyanide

23. E t h o x y e t hmercury
yl chloride

50. Sodium flouroac

24. Ethyl fonnate

51. Sodium fluorosietate

25. Ethyl mercury acetate

52. Sulphurlicate

26. Ethyl mercury bromide

53. Tar acid

27. Ethyl mercury chloride

54. Zinc phosphide

Brueau of Indian Standards

BIS is a statutory institution established under the Bureau of Indian Standards Act, 1986 to promote
harmonious development of the activities of standardization, marking and qualit!. certification of goods
and attending to connected matters in the country.
Copyrigbl
BIS has the copyright
form without the prior
of implementing the
designations. Enquiries

of all its publications. No part of these publications

permission in writing of BIS. This does not preclude
standard, of necessary details, such as symbols
relating to copyright be addressed to the Director (

may be reproduced in any

the free use, in the course
and sizes, type or grade
Publications ), BIS.

Review of Indian Standards

Amendments are issued to standards as the need arises on the basis of comments. Standards are also
reviewed periodically; a standard along with amendments is reaffirmed when such review indicates that
no changes are needed; if the review indicates that changes. are needed, it is taken up for revision.
Users of Indian Standards should ascertain that they are in possession of the latest amendments or
edition.
This Indian Standard has been developed from Dot : No. FAD I ( 4009 ).

Amendments Issued Since Publication

Date of Issue

Amend No.

Text Affected

BUREAU OF INDIAN STANDARDS

Headquarters:
Telegrams : Manaksanstha .
( Common to all offices )

Manak Bhavan, 9 Bahadur Shah Zafar Marg, New Delhi 1 lb002

Telephones : 331 01 31, 331 13 75

Telephone

Regional Offices :

331 01 31
331 13 75

Central : Manak Bhavan, 9 Bahadur Shah Zafar Marg

_. I
NEW DELHI 110002
- ** !
Eastern : l/14 C. I. T. Scheme VII M, V. I. P. Road, Maniktola
_I
CALCUTTA 700054
_
Northern : SC0 445-446, Sector 35-C, CHANDIGARH 160036
_

Southern : C. I. T. Campus, IV Cross Road, MADRAS 600113

Western : Manakalaya, E9 MIDC, Marol, Andheri ( East )
BOMBAY 400093

..

.37 84 99, 37 85 61
37 86 26, 37 86 62
53 38 43, 53 16 40
53 23 84

I 235 02 16, 235 04 42

235 15 19, 235 23 15
632 92 95, 632 78 58
632 78 91, 632 78 92

..

BHUBANESHWAR.
BANGALORE. BHOPAL.
Branches : AHMADABAD.
COIMBATORE. FARIDABAD. GHAZIABAD. .GUWAHATI. HYDERABAD.
J A I P U R . K A N P U R . LUCKNOW. . P A T N A . THIRUVANANTHAPURAM.
.
9
e

..!;*;,.

Pri@d ~$EW h~dfhP*~ P~E%E, Ehurja, India

..-

_,
i

. _,*
---

.I.
.

.;.*