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2014 WPC recap
Global perfumery summit
cis-Jasmone in avors
Biotechnology-derived ingredients,
mountain savory oil, avor and
fragrance materials, and more.
NATURALS IN F&F
PF1409_Cover.indd 1 8/6/14 1:38 PM
2014 Sigma-Aldrich Co. LLC. All rights reserved. SIGMA-ALDRICH is a trademark of Sigma-Aldrich Co. LLC, registered in the US and other countries.
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Untitled-1 1 7/25/14 9:29 AM
2 Vol. 39 September 2014 | Perfumer & Flavorist www.PerfumerFlavorist.com
VOL. 39 SEPTEMBER 2014
FLAVOR
30
cis-Jasmone
John Wright
This ingredient excels in fruit avors, adding a level of depth,
realism and complexity that has few rivals.
66
Organoleptic Characteristics of Flavor Materials
Judith Michalski
Methyl laurate, ethyl phenylacetate, 2-octanone, isophorone
and more.
FRAGRANCE
38
2014 World Perfumery Congress Addresses Rapid Changes
Impacting Global Industry
Victoria Frolova
Focused on regulations, innovation, sustainability and new
markets, the WPC provided inspiration for the industrys
creative minds.
56
International Perfumer Meeting: Enhancing the Recognition of
Perfumery Worldwide
The rst meeting of the international societies of perfumers,
held at the 2014 World Perfumery Congress, addressed global
cooperation to support perfumery.
58
2014 World Perfumery Congress Exhibition News & Notes
Photos and company news from the exhibition oor.
80
The Last Word: Honoring Contributions to Perfumer Societies
& Perfumery
INGREDIENTS
26
Raw Material Bulletin
Passion fruit aroma, cinnamyl acetate, Karmawood, dimethyl
sulde and more.
32
Biotechnology Enters Its Next Phase
Recent ingredient launches signal increasing complexity of
biotechnologically derived avor and fragrance materials.
68
Progress in Essential Oils
Brian M. Lawrence
Mountain savory oil.
INDUSTRY
6
Editors Note: Perfumery, Acquisitions & More
8
Industry: News, Events and Analysis
25
Events
77
Worldwide Sources
79
Ad Index
ON THIS MONTHS COVER
This month, P&F explores naturals in F&F, including
biotechnology-derived natural ingredients (Page 32),
mountain savory oil (Page 68), and avor and fragrance
materials from various sources (Pages 26 and 66).
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warmth of amber and a dark woody character
reminiscent of patchouli.
Clearwood
b-bisabolene (1.1%)
geranyl acetate (2.1%)
nerol (1.1%)
geraniol (5.0%)
thymol (45.2%)
carvacrol (5.3%)
(0.9%)
caryophyllene oxide (1.1%)
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Untitled-1 1 7/25/14 9:30 AM
72 Ingredients Vol. 39 September 2014 | Perfumer & Flavorist www.PerfumerFlavorist.com
in T-3. The trace components (<0.5%)
that were reported to be characterized
in one or both oils were cis-p-mentha-
2,8-dien-1-ol, piperitenone oxide,
a-calacorene, 1-epi-cubenol, T-cadinol
and 14-hydroxy-a-muurolene.
A carvacrol-rich commercial oil of S.
montana of Slovenian origin was ana-
lyzed using GC-FID and GC/MS by
Stoilova et al. (2008). The constituents
characterized in this oil were as follows:
a-thujene (0.6%)
a-pinene (2.8%)
camphene (0.6%)
sabinene (0.1%)
1-octen-3-ol (1.1%)
b-pinene (0.2%)
myrcene (1.1%)
3-octanol (0.5%)
a-phellandrene (0.5%)
p-cymene (11.0%)
a-terpinene (1.3%)
limonene (1.3%)
1,8-cineole (1.0%)
(Z)-b-ocimene (2.1%)
(E)-b-ocimene (0.1%)
g-terpinene (6.2%)
trans-sabinene hydrate (0.1%)
terpinolene (0.2%)
cis-sabinene hydrate (0.7%)
linalool (1.6%)
a-thujone (0.1%)
camphol (0.8%)
borneol (2.4%)
terpinen-4-ol (0.5%)
g-terpineol
(0.2%)
a-terpineol (1.4%)
methyl carvacrol (0.6%)
neral (0.1%)
geraniol (0.1%)
carvone (0.5%)
piperitone (0.1%)
geranial (0.1%)
thymol (8.6%)
carvacrol (41.5%)
carvacrol acetate (0.1%)
geranyl acetate (0.1%)
b-bourbonene (0.1%)
b-caryophyllene (4.1%)
a-humulene (0.3%)
aromadendrene (0.2%)
germacrene D (0.1%)
bicyclogermacrene (0.1%)
b-bisabolene (1.0%)
0.1 -
trans-p-menth-2-en-1-ol t 0.5
trans-verbenol 0.2 0.2
borneol 2.9 4.8
cis-linalool oxide
p
0.2 -
trans-linalool oxide
p
0.2 -
terpinen-4-ol 0.8 10.3
p-cymen-8-ol 1.8 1.4
a-terpineol 1.9 1.5
cis-piperitol - 0.2
myrtenol - 0.1
trans-piperitol 0.1 0.4
nerol - 2.0
methyl thymol - 0.5
trans-chrysanthenyl acetate
- 0.1
cuminaldehyde t 0.2
neral - 0.5
methyl carvacrol - 1.1
thymoquinone 2.8 0.1
geraniol 0.1 22.3
geranial - 1.1
2-ethyl menthone
0.2 -
bornyl acetate - 0.1
thymol 31.7 3.8
o-acetanisole
- 0.4
cuminyl alcohol - 0.2
carvacrol 23.3 10.6
cis-piperityl acetate - 0.1
a-terpinyl acetate - 0.1
thymol acetate 0.1 -
eugenol 0.1 t
a-copaene - 0.1
b-bourbonene - 0.4
geranyl acetate - 0.1
b-elemene - 0.1
b-caryophyllene - 2.9
b-copaene - 0.1
aromadendrene - 0.1
4-t-butylcatechol
1.1 -
a-humulene - 0.1
allo-aromadendrene - 0.1
g-muurolene - 0.1
germacrene D - 1.9
bicyclogermacrene - 1.0
b-bisabolene - 0.7
g-cadinene - 0.1
PF1409_Lawrence_fcx.indd 72 8/6/14 2:07 PM
73
was hydrodistilled for 2 hr. The oil, which
was analyzed by Vidic et al. (2009) using
GC/MS only, was determined to possess
the following composition:
1-octen-3-ol (1.4%)
3-octanol (0.2%)
a-terpinene (0.1%)
p-cymene (0.3%)
1,8-cineole (0.1%)
g-terpinene (0.1%)
cis-sabinene hydrate (0.3%)
trans-sabinene hydrate (0.1%)
linalool (0.3%)
cis-p-menth-2-en-1-ol (0.1%)
trans-p-menth-1-en-1-ol (0.1%)
camphor (0.1%)
borneol (5.3%)
terpinen-4-ol (1.0%)
p-cymen-8-ol (0.2%)
a-terpineol (0.3%)
cis-dihydrocarvone (0.1%)
trans-dihydrocarvone (0.1%)
methyl thymol (0.3%)
methyl carvacrol (0.5%)
thymoquinone (0.6%)
thymol (20.1%)
carvacrol (59.1%)
thymol acetate (0.2%)
carvacrol acetate (0.3%)
b-caryophyllene (1.8%)
a-gurjunene (0.1%)
aromadendrene (0.4%)
a-humulene (0.1%)
allo-aromadendrene (0.1%)
g-muurolene (0.1%)
viridiorene (0.2%)
b-bisabolene (2.0%)
d-cadinene (0.1%)
thymohydroquinone (0.2%)
spathulenol (0.6%)
caryophyllene oxide (1.9%)
globulol (0.1%)
cubeban-11-ol (0.1%)
rosifoliol (0.1%)
humulene epoxide II (0.1%)
14-hydroxy-9-epi-b-caryophyllene (0.2%)
epi-a-bisabolol (0.1%)
Tr ace amount s ( <0. 1%) of
trans-piperitol, isobornyl formate, cis-
piperitenone oxide, bornyl acetate,
b-bourbonene, b-cubebene, g-amorphene,
a-muurol ene, g-cadi nene, trans-
cycloisolongifol-5-ol (doubtful correct
identication), a-cadinene, a-calacorene,
caryophylla-4(12),8(13)-dien-5a-ol,
caryophylla-4(12),8(13)-dien-5b-ol and
T-muurolol were also reported as con-
stituents of this oil.
A lab-distilled oil of Satureja montana,
which was produced from dried leaves
grown in Evora (Portugal), was screened
T-3. Comparative percentage composition of the oils of two populations of
Satureja montana from Bosnia Herzegovina (Cont.)
Compound Population 1 oil Population 2 oil
butylated hydroxytoluene
0.1 0.1
d-cadinene t 0.2
dihydroactinodiolide
0.4 0.1
a-cadinene - 0.1
salviadienol
*
- 0.1
(E)-nerolidol 0.3 -
spathulenol 3.0 3.1
caryophyllene oxide 7.7 5.2
viridiorol 0.3 -
salvial-4(14)-en-1-one t 0.2
humulene epoxide II 0.3 0.3
guaia-6(10),14-dien-4b-ol - 0.1
torilenol 0.2 0.3
caryophylla-3(15),7(14)-dien-6a-ol 0.5 0.1
caryophylla-3(15),7(14)-dien-6b-ol 2.2 0.4
isospathulenol t 0.2
3-isothujopsanone
0.2 0.2
b-eudesmol 0.2 -
a-cadinol 0.5 -
14-hydroxy-b-caryophyllene 2.6 0.4
14-hydroxy-9-epi-b-caryophyllene 4.1 0.8
khusinol
0.5 0.4
6a-hydroxygermacra-1(10),4-diene
- 0.1
eudesma-4(15),7-dien-1b-ol t 0.1
oplopanone 0.1 -
benzyl benzoate 0.2 -
hexadecanoic acid 1.0 -
heneicosane t 0.1
docosane t 0.2
tricosane 0.1 0.6
tetracosane 0.3 1.2
pentacosane 0.3 1.6
hexacosane 0.3 2.4
incorrect identication
*
correct isomer not determined
f
furanoid form
p
pyranoid form
t=trace (<0.05%)
supercritical fluid CO
2
extracts of S.
montana (performed under different
pressures) collected at their full ower-
ing stage from a medicinal garden at Ejea
(Spain). The results of the analyses per-
formed using GC-FID and GC/MS can
be seen summarized in T-4. The yield of
oil from the dried plant material, which
was reduced to different particle sizes
(0.4, 0.6 and 0.8 mm), was 1.11.6%;
the smaller the particle size, the higher
the oil yield. The yield of volatiles found
in the supercritical uid extracts ranged
from 0.91.8%, the highest being found
with dried plant material with a mean
particle size of 0.6 mm at 40C and 100
bar pressure, and a 1.1 kg/hr ow rate
of CO
2
.
Silva et al. (2009) also compared the
compositions of a hydrodistilled oil and a
supercritical uid extract of S. montana;
however, these results were previously
published by Grosso et al. (2009).
Satureja montana plants collected
at the commencement of flowering
near the village of Pijavicino (Peljesac
Peninsula, Croatia) were dried at
ambient temperatures, and a 10 g sample
PF1409_Lawrence_fcx.indd 73 8/6/14 2:07 PM
74 Ingredients Vol. 39 September 2014 | Perfumer & Flavorist www.PerfumerFlavorist.com
for its nematicidal activity by Barbosa et
al. (2010). Analysis of this oil by GC-FID
and GC/MS revealed that it possessed
the following composition:
a-thujene (2.3%)
a-pinene (1.5%)
camphene (0.1%)
1-octen-3-ol (0.3%)
b-pinene (0.5%)
myrcene (2.5%)
a-phellandrene (0.4%)
d-3-carene (0.1%)
a-terpinene (4.1%)
p-cymene (7.1%)
b-phellandrene (0.2%)
limonene (0.4%)
g-terpinene (39.8%)
trans-sabinene hydrate (0.6%)
cis-sabinene hydrate (0.1%)
borneol (0.1%)
terpinen-4-ol (0.4%)
methyl carvacrol (0.2%)
carvacrol (38.8%)
b-caryophyllene (0.5%)
Trace amounts (<0.05%) of 3-octanol,
(E)-b-ocimene, terpinolene, cis-dihy-
drocarvone, a-terpineol, thymol and
b-bisabolene were also found in this oil.
Grosso et al. (2010) screened the oil
and supercritical uid CO
2
extract for
their anticholinesterase and antimicro-
bial activities. They reported the same
compositional data, as was reported by
Grosso et al. (2009) and Silva (2009).
Finally, a summary of the published
data on the composition of savory oil
(Lawrence, 1979, 1981, 1988, 1992,
1996, 2003) reveals that S. montana
oil possesses six chemotypic forms. A
comparison of the major components
found in these six chemotypic oils is
shown in T-5.
L.G. Angelini, G. Carpanese, P.L. Cioni, I. Morelli,
M. Macchia and G. Flamini, Essential oils
from Mediterranean Lamiaceae as weed
germination inhibitors. J. Agric. Food Chem.,
51, 61586164 (2003).
R. Chizzola, Volatile oil composition of four
populations of Satureja montana L. from
southern France. Acta Hort., 598, 143147
(2003).
A. Radonic and M. Milos, Chemical composition and
in vitro evaluation of antioxidant effect of free
volatile compounds from Satureja montana L.
Free Radical Res., 18, 17 (2003).
M. Skocibusic and N. Bezic, Phytochemical analysis
and in vitro antimicrobial activity of two
Satureja species essential oils. Phytotherap.
Res., 967970 (2004).
T-4. Comparative percentage composition of the oil and the volatiles of supercritical
uid CO
2
extracts of Satureja montana produced under different pressures
T-5. Percentage composition of the oils of six chemical forms of Satureja montana
Compound Oil SFE 90 bar SFE 100 bar
a-thujene 0.40.6 0.10.3 0.20.3
a-pinene 0.40.7 00.3 0.2
camphene 0t 00.1 0t
sabinene 0.10.2 00.1 t0.1
1-octen-3-ol 0.10.2 t0.2 0.1
b-pinene 0.50.8 0.40.6 0.71.2
myrcene 0.71.1 0.30.6 0.40.8
a-phellandrene 0.2 0.10.2 0.10.3
d-3-carene t0.1 0t t
a-terpinene 1.21.8 0.71.4 1.01.9
p-cymene 6.912.8 6.010.9 8.917.8
1,8-cineole 0.30.5 0.20.4 0.30.6
b-phellandrene 0.30.5 0.20.4 0.30.6
limonene 0.20.4 0.10.3 0.3
(Z)-b-ocimene 00.1 00.1 -
g-terpinene 6.49.4 2.35.5 3.16.0
trans-sabinene hydrate 0.40.5 0.30.7 0.30.6
terpinolene 0.2 0.10.2 0.10.3
cis-sabinene hydrate 0.1 00.2 0.1
linalool 0.60.8 0.51.1 0.91.0
borneol 0.70.8 0.70.9 0.60.8
terpinen-4-ol 0.60.7 0.4 0.40.6
a-terpineol 0.2 0.10.2 0.20.3
carvone 00.1 0.10.3 0.10.3
thymoquinone 0.2 1.63.1 2.52.9
methyl carvacrol 0.1 - 0t
thymol 8.611.0 6.010.9 9.111.3
carvacrol 52.262.0 52.764.5 41.752.8
b-bourbonene t0.1 t0.1 0.1
b-caryophyllene 1.31.5 1.41.5 1.32.1
trans-a-bergamotene 0.10.2 t0.3 t0.5
g-muurolene 0.1 00.2 0.1
germacrene D 0.20.3 00.3 0.30.5
b-bisabolene 2.02.7 2.53.0 2.23.5
d-cadinene 0.2 00.2 0.20.3
thymohydroquinone 0.30.4 0.30.5 0.40.6
caryophyllene oxide 0.20.3 0.10.2 0.10.2
a-bisabolol 0t 0t 0t
t=trace (<0.05%)
Compound 1 2 3 4 5 6
a-pinene 0.41.4 t1.1 1.71.8 0.1 0.4 0.2
myrcene t0.2 t1.2 t0.2 0.1 0.51.9 4.9
g-terpinene 3.510.3 1.815.1 8.111.6 1.3 1.96.4 1.0
p-cymene 2.513.0 2.214.6 4.68.9 0.9 3.712.5 0.6
linalool 0.30.6 0.10.6 0.20.4 72.2 27.829.9 0.6
terpinen-4-ol 0.11.2 3.14.1 0.10.6 8.5 6.811.5 14.9
a-terpineol 0.33.1 2.44.4 0.20.7 1.9 11.527.7 18.0
thymol 53.565.7 1.08.0 22.342.6 0.6 2.29.0 14.5
carvacrol t6.8 46.575.0 17.631.0 t 04.2 3.7
t=trace amount (<0.05%)
PF1409_Lawrence_fcx.indd 74 8/6/14 2:07 PM
Speaker Lineup:
Ken Bickerton, CIH, CSP, Phase Associates LLC
Patrick McNamara, Scarinci & Hollenbeck
William Brugger, Ph.D., Global Directions, Inc.
Mike Bloom, Flavor & Fragrance Specialties
Craig Hagelin, Frutarom USA
Joe Piazza, Comax Flavors
Henry Sethness, Sethness Products Company
Steve Somers, Vigon International
John Wright, Flavorist
Steve Pearce, Omega Ingredients Ltd.
Chef Gary Patterson, McCormick & Co.
How FIavor & Ingredient Companies are Meeting
Customers' New Food Safety Requirements
97
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October 23-26, 2014
The Resort at Longboat Key CIub,
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Presentations & nteractive Sessions:
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Untitled-5 1 7/24/14 11:46 AM
76 Ingredients Vol. 39 September 2014 | Perfumer & Flavorist www.PerfumerFlavorist.com
M. Skocibusic and N. Bazic, Chemical composition
and antimicrobial variability of Satureja
montana L. essential oils produced during
ontogenesis. J. Essent. Oil Res., 16, 387391
(2004).
D.I. Bezbradica, J.M. Tomovic, M.S. Vukasinovic, S.
Siler-Marinkovic and M.M. Ristic, Composition
and antimicrobial activity of essential oil of
Satureja montana L. collected in Serbia and
Montenegro. J. Essent. Oil Res., 17, 462465
(2005).
S. Cavar, M. Maksimovic, M.E. Solic, A. Jerkovic-
Mujkic and R. Besta, Chemical composition
and antioxidant and antimicrobial activity of
two Satureja essential oils. Food Chem., 111,
648653 (2008).
R. Omidbaigi, S. Rahimi and Sh. Kazemi,
Comparison between essential oil content
and compositions of winter (perennial) and
summer (annual) savory. J. Essent. Oil Bear.
Plants, 10, 480485 (2007).
I. Stoilova, S. Bail, G. Buchbauer, A. Krastanov,
A. Stoyanova, E. Schmidt and L. Jirovetz,
Chemical composition, olfactory evaluation
and antioxidant effects of the essential oil of
Satureja montana L. Nat. Prod. Comm., 3,
10351042 (2008).
C. Grosso, A.C. Figueiredo, J. Burillo, A.M.
Mainar, J.S. Urieta, J.G. Barroso, J.A. Coelho
and A.M.F. Palavra, Enrichment of the
thymoquinone content in volatile oil from
Satureja montana using supercritical uid
extraction. J. Sep. Sci., 32, 328334 (2009).
F.V.M. Silva, A. Martins, J. Salta, N.R. Neng, J.M.F.
Nogueira, D. Mira, N. Gaspar, J. Justino,
C. Grosso, J.S. Urieta, A.M.S. Palavra and
A.P. Rauter, Phytochemical profile and
anticholinesterase and antimicrobial activities
of supercritical versus conventional extracts
of Satureja montana. J. Agric. Food Chem.,
57, 1155711563 (2009).
D. Vidic, M. Maksimovic, S. Cavar and M.E.
Solic, Comparison of essential oil proles of
Satureja montana L. and endemic Satureja
visianii Silic. J. Essent. Oil Bear. Plants, 12,
273281 (2009).
P. Barbosa, A.S. Lima, P. Viera, L.S. Dias, M.T.
Tinoco, J.G. Barbosa, L.G. Pedro, A.C.
Figueiredo and M. Mota, Nematicidal
activity of essential oils and volatiles derived
from Portuguese aromatic flora against
the pinewood nematode Bursaphelenchus
xylophilus. J. Nematology, 42, 816 (2010).
C. Grosso, J.A. Coelho, J.S. Urieta, A.M.F. Palavra
and J.G. Barroso, Herbicidal activity of
volatiles from coriander, winter savory,
cotton lavender and thyme isolated by
hydrodistillation and supercritical fluid
extraction. J. Agric. Food Chem., 58,
1100711013 (2010).
B.M. Lawrence, Savory oil. In: Progress in Essential
Oils. Perfum. Flav., 3(6), 5758 (1979); 6(4),
7677 (1981); 13(1), 4658 (1988); 17(1),
5254 (1992); 21(6), 5557 (1996); 28(6),
5863 (2003).
To purchase a copy of this article or others,
visit www.PerfumerFlavorist.com/magazine.
PF1409_Lawrence_fcx.indd 76 8/6/14 2:07 PM
77
CHINA EGYPT
HAITI
Worldwide Sources
INDIA
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79
Advertiser Web site Page
Advanced Biotech www.adv-bio.com 23
Alluredbooks www.Alluredbooks.com 79
Axxence Aromatic GmbH www.axxence.com 49
Bedoukian Research, Inc. www.bedoukian.com 63
Berj, Inc. www.berjeinc.com 15
Cedar Oil Works LLC www.cedaroilworks.com 57
Dhler Group www.doehler.com 71
drom fragrances international www.drom.com 69
DRT www.drt-france.com 76
Ernesto Ventos SA www.ventos.com 4041
Excellentia International www.excellentiaint.com 37
Firmenich, Inc. www.rmenich.com 39
Fleurchem, Inc. www.eurchem.com 31
Fricke Abfulltechnik GmbH & Co. www.fricke-dos.com 53
Galen-N www.galen-n.com 25
Global Essence, Inc. www.globalessence.com 17
Gulcicek Kimya www.gulcicek.com 5
Gusmer Enterprises, Specialty Products www.gusmerenterprises.com 36
Hangzhou Grascent Co., Ltd. www.grascent.com 55
I.P. Callison & Sons www.ipcallison.com 57
Indesso Aroma, PT www.indesso.com 43
Indukern www.indukern-fngredients.com 2829
International Flavors & Fragrances, Inc. www.iff.com 21
Kunshan Monza Import & export Co. Ltd. www.ksmonza.com 67
Les Aromes du Maroc www.aromes.ma 59
Mane USA www.mane.com 7
Mitsubishi Gas Chemical America, Inc. www.aromaticchemicals.com 24
NAFFS www.naffs.org 75
Natural Advantage www.natural-advantage.net 11
Norex Flavours Pvt. Ltd. www.menthol-mint.com 27
Penta Manufacturing Co. www.pentamfg.com Cover 4
PT Van Aroma www.vanaroma.com 64
Renessenz www.renessenz.com 3
Robertet SA www.robertet.com 45
Sigma Aldrich Flavors & Fragrances www.sigma-aldrich.com/avors-fragrances Cover 2
SAF-ISIS USA www.sasis.com 33
Som Extracts Limited www.somextracts.com 24
Sonarome Pvt. Ltd. www.sonarome.com 61
Symrise www.symrise.com 1
Takasago Intl Corp. www.takasago.com 51
Ultra International Ltd. www.ultrainternational.com 35
Vigon International, Inc. www.vigoninternational.com Cover 3
Xiamen Bestally Biotechnology Co., Ltd. www.bestally.com.cn 65
Ad Index
PF1409_Ad Index_fcx.indd 79 8/6/14 3:13 PM
80 The Last Word Vol. 39 September 2014 | Perfumer & Flavorist www.PerfumerFlavorist.com
This conversation brought to you by:
We make it happen . . . together.
Honoring Contributions to Perfumer
Societies & Perfumery
T
he 2014 World Perfumery Congress (WPC) celebrated
perfumery and the perfumers, in addition to hosting
the rst meeting of global perfumery societies, which
included the Socit Franaise des Parfumeurs (SFP), Deutsche
Gesellschaft der Parfmeure in der SEPAWA (DGP), British
Society of Perfumers (BSP) and American Society of Perfumers
(ASP).
On the closing day of the conference, the ASP and SFP
presented their awards, which recognized achievements in
fragrance creation and devotion to service.
First, Sylvie Jourdet (president of the SFP; Crassence),
Maurice Roucel (SFP; Symrise), and Patrick de Vilmorin (SFP;
Firmenich) introduced the winner of the Prix International du
Parfumeur Crateur 2014. The award honors perfumers 35
years old and younger, who are encouraged to freely express
their creativity.
Designed by Chanel, the trophy symbolized the dedication
and perseverance required to create great fragrances, Vilmorin
noted, as well as the complexity, richness and uniqueness of
fragrance.
This years winner was Alice Lavenat, junior perfumer
with Jean Niel. Her fragrance was selected following two jury
reviews, one of which was technical, comprising perfumers and
evaluators, and a second, which evaluated the scent submissions
on an artistic level from the point of view of the customer.
All scents were built around bourgeons de cassis (blackcurrant
buds) absolute.
Next, Chris Diienno (president of ASP; drom) presented
the 2014 William Lambert Award to Jim Fassold (nancial
administrator of ASP; Robertet). Diienno called Fassold a man
you can count on.
Diienno continued, He can keep a condence, and can nd
common ground with anyone. In Jims mind, difcult personali-
ties are just challenges to be won over. He is generous with his
time and knowledge and always has an open door to a colleague
who needs nancial advice or otherwise.
Finally, in honor of its 50th anniversary, the BSP launched
British PerfumeryA Fragrant History (www.bsp.org.uk/bsp-
book-2/) and presented it at the WPC. The book is a celebration
of British perfumery past and present, inviting readers to share
personal stories and experiences of the many perfumers who,
over the years, have made British perfumery as full of creativity
and talent as it is today.
From left: Sylvie Jourdet (president of the SFP; Crassence); Maurice Roucel
(SFP; Symrise); Prix International du Parfumeur Crateur 2014 winner, Alice
Lavenat (Jean Niel); and Patrick de Vilmorin (SFP; Firmenich).
From left: Jim Fassold (ASP; Robertet), recipient of the William Lambert Award,
and Chris Diienno (ASP president; drom).
PF1409_Last Word_fcx.indd 80 8/6/14 2:12 PM
Untitled-4 1 8/6/14 2:29 PM
50 Okner Parkway, Livingston, New Jersey 07039-1604 Phone: (973) 740-2300 Fax: (973) 740-1839
E-Mail: sales@pentamfg.com Web: www.pentamfg.com
Developing Better Products
through Natural Chemistry
Penta Manufacturing Company is Family Owned and Operated for Over 30 Years.
For a complete list of all our natural, natural identical & synthetic ingredients
visit us at our web: www.pentamfg.com
Here is a partial listing of our Naturally derived avor & fragrance ingredients.
All items are Food Grade Kosher & Organic Compliant.
A Division of Penta International Corporation
Penta Manufacturing Company
Acetal
Acetic Acid
Acetol
Acetone
Acetyl Butyryl
Allyl Heptoate
Acetophenone
Alpha-Damascone
Beta-Damascone
3,4-Dimethyl-1,2-
Cyclopentadione
Dimethyl Disulde
Cis-Jasmone
Mesityl Oxide
Methyl Alcohol
Myrcene
Delta-Nonalactone
CIS-6-NONENAL
CIS-6-NONENOL
4-Nonanone
Cis-6-Nonenal
3-Nonen-2-One
2,4-Octadienal
3-Octanol
Trans-2-Octenal
2-Octen-4-One
3-Octyl Acetate
Octyl Butyrate
Oleic Acid
Piperine
Prenyl Acetate
Prenyl Mercaptan
L-Proline
Propionaldehyde
Propionic Acid
2-Propionyl
Thiophene
Propyl Acetate
Propyl Alcohol
Propyl Butyrate
Propyl Caproate
Propyl Caprylate
Propyl Disulde
Propylene Glycol
Propyl Isobutyrate
Propyl Mercaptan
Propyl-
2-MethylButyrate
Propyl
ThioAcetate
D-Pulegone
Pyrazine
Ethanethiol
2-Pyridine
Methanethiol
Quinine
Rhodinol
D-Ribose
Rum Ether
Safranal
Sclareolide
Skatole
Stearic Acid
Styrallyl Acetate
Styrallyl Alcohol
Styrallyl
Isobutyrate
Succinic Acid
Gamma-
Terpinene
Terpinyl Acetate
Delta-
Tetradecalactone
5,6,7,8-Tetrahy-
droquinoxaline
2,3,5,6-Tetramethyl
Pyrazine
Theaspirane
Theobromine
2,2-
(Thiodimethylene)
Difuran
Thiogeraniol
Thiophenol
Thymol Crystals
Delta-
Tridecalactone
Triethyl Citrate
2,4,6-Triisobutyl-
5,6-dihydro-4h-
1,3,5-dithiazine
Trimethylamine
2,6,6-
Trimethylcyclohex-
2-ene-1,4-dione
2,3,5-Trimethyl
Pyrazine
2,4,5-Trimethyl
Thiazole
Trithioacetone
Turpentine
L-Tyrosine
2,4-Undecadienal
Delta-
Undecalactone
Trans-2-
Undecenal
Undecylenic Acid
Valencene
Gamma-
Valerolactone
Valeraldehyde
Valeric Acid
Valspice
Vanillin
Vanillin Acetate
Vanillin
Isobutyrate
4-Vinyl Guaiacol
Vitamin E
Wintergreen Oil
Xylitol
D-Xylose
Zingerone
PF1409_Penta.indd 1 7/21/14 3:35 PM