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The Good Scents Company - Aromatic/Hydrocarbon/Inorganic Ingredients Catalog information

phenoxyacetaldehyde 50% in benzyl alcohol
cortex aldehyde 50 (IFF)

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    2120-70-9 Acetaldehyde,2-phenoxy- 95%
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    16-18540 PHENOXY ACETALDEHYDE 50% IN BENZYL ALCOHOL
  • The John D. Walsh Company

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    The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
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    History
    CODE101881 CODE101881
    Product(s):
    Cortex Aldehyde 50% Benzyl Alcohol
    SDS
  • Ernesto Ventós

Name:2-phenoxyacetaldehyde
CAS Number: 2120-70-9Picture of molecule3D/inchi
% from:50.00%
ECHA EINECS - REACH Pre-Reg:218-329-5
FDA UNII: Search
Nikkaji Web:J33.410C
Beilstein Number:0970857
MDL:MFCD00134414
XlogP3:1.80 (est)
Molecular Weight:136.15016000
Formula:C8 H8 O2
NMR Predictor:Predict (works with chrome, Edge or firefox)
Also(can) Contains:benzyl alcohol 50.00%

Category: fragrance agents

US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:

Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search

Physical Properties:

Appearance:colorless clear viscous liquid (est)
Assay: 45.00 to 55.00
Food Chemicals Codex Listed: No
Specific Gravity:1.12000 to 1.14000 @ 25.00 °C.
Pounds per Gallon - (est).: 9.320 to 9.486
Specific Gravity:1.12100 to 1.14100 @ 20.00 °C.
Pounds per Gallon - est.: 9.339 to 9.505
Refractive Index:1.54500 to 1.56500 @ 20.00 °C.
Boiling Point: 220.39 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.113000 mmHg @ 25.00 °C. (est)
Flash Point: 185.00 °F. TCC ( 85.00 °C. )
logP (o/w): 1.134 (est)
Soluble in:
 alcohol
 water, 1.048e+004 mg/L @ 25 °C (est)
Insoluble in:
 water
Similar Items:note
para-anisyl acetaldehyde
cumin acetaldehyde
cuminyl acetaldehyde
lilac acetaldehyde
mercaptoacetaldehyde
phenoxyacetaldehyde 50% in peomosa
phenyl acetaldehyde
pinoacetaldehyde

Organoleptic Properties:

Odor Type: green
Odor Strength:medium ,
recommend smelling in a 10.00 % solution or less
Substantivity:188 hour(s) at 100.00 %
fresh green cortex leafy hyacinth ozone leathery
Odor Description:at 10.00 % in dipropylene glycol. fresh green cortex leafy hyacinth ozone leather
Luebke, William tgsc, (1990)
Odor sample from: International Flavors & Fragrances Inc.
Flavor Type: green
green cortex leafy melon rind watery phenolic
Taste Description: green cortex leafy melon rind watery phenolic
Luebke, William tgsc, (1990)
Odor and/or flavor descriptions from others (if found).
IFF
Cortex Aldehyde 50% Benzyl Alcohol
Odor Description:Green (stem like), floral (flower shop). Used in fragrances to give 'outdoors' character and freshness

Cosmetic Information:

Suppliers:

Augustus Oils
Cortex Aldehyde 50
Services
Azelis UK
Cortex ald benz alc 50 PCT
BOC Sciences
For experimental / research use only.
Acetaldehyde,2-phenoxy- 95%
Ernesto Ventós
ALDEHYDE CORTEX 50 IFF

Odor: GREEN, FLORAL, SAPPY-GREEN, WOOD

IFF
Cortex Aldehyde 50% Benzyl Alcohol

Odor: Green (stem like), floral (flower shop). Used in fragrances to give 'outdoors' character and freshness

Lluch Essence
CORTEX ALDEHYDE 50% BENZYL ALCOHOL

Odor: FLORAL, HYACINTH, GREEN

M&U International
Cortex Aldehyde 50 Benzyl Alcohol
Moellhausen
ALDEHYDE CORTEX
Penta International
PHENOXY ACETALDEHYDE 50% IN BENZYL ALCOHOL
Sigma-Aldrich: Aldrich
For experimental / research use only.
Phenoxyacetaldehyde
The John D. Walsh Company
Cortex Aldehyde 50% Benzyl Alcohol

Safety Information:

Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for phenoxyacetaldehyde 50% in benzyl alcohol usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Recommendation for phenoxyacetaldehyde 50% in benzyl alcohol flavor usage levels up to:
 not for flavor use.

Safety References:

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):2120-70-9
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :75033
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
2-phenoxyacetaldehyde
Chemidplus:0002120709
RTECS:AB2990000 for cas# 2120-70-9

References:

Other Information:

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):Search
ChemSpider:View

Potential Blenders and core components note

For Odor
aldehydic
muguet undecadienal
FR
animal

para-

cresyl phenyl acetate
FL/FR
balsamic
cinnamyl alcohol
FL/FR

3-

phenyl propyl alcohol
FL/FR

2-

phenyl propyl alcohol
FL/FR
propyl cinnamate
FL/FR
tetrahydrofurfuryl cinnamate
FL/FR
chemical
styralyl alcohol
FL/FR
citrus
neroli ketone
FR
petitgrain combava oil
FR
fatty

(E)-2-

octenal
FL/FR
fermented
hexanal diethyl acetal
FL/FR
floral
allyl anthranilate
FL/FR
anisyl propanal / methyl anthranilate schiff's base
FR
dimethyl benzyl carbinol
FL/FR

2,4-

dimethyl cyclohexyl methyl acetate
FR
ethyl hydrocinnamate
FL/FR
floral fragrance
FR
hyacinth ether
FR
hyacinth fragrance
FR
hyacinth specialty
FR
kewda oil
CS

para-

methyl benzyl acetate
FL/FR
narcissus absolute replacer
FR
narcissus fragrance
FR
narcissus specialty
FR
ocean propanal / methyl anthranilate schiff's base
FR

bitter

orangeflower absolute morocco
FL/FR

bitter

orangeflower absolute tunisia
FL/FR
phenethyl formate
FL/FR
phenethyl salicylate
FL/FR
phenyl acetaldehyde / methyl anthranilate schiff's base
FR
phenyl acetaldehyde diisobutyl acetal
FL/FR
phenyl glycol diacetate
FR

2-

phenyl propionaldehyde dimethyl acetal
FL/FR

2-

phenyl propyl acetate
FL/FR

(R)-2-

phenyl propyl alcohol
FL/FR

3-

phenyl propyl formate
FL/FR
phenyl propyl phenyl acetate
FR

3-

phenyl propyl propionate
FL/FR

(E)-2-

phenyl-1(2)-propene-1-yl acetate
FR

iso

propyl phenyl acetate
FL/FR
reseda absolute
FR
reseda absolute replacer
FR
reseda acetal
FR
rose absolute (rosa damascena) bulgaria
FL/FR

laevo-

rose oxide
FL/FR
tea acetate
FR
fresh

3-(3-

propen-2-yl phenyl) butanal
FR
fruity
acetaldehyde dihexyl acetal
FL/FR
benzyl methyl ether
FL/FR
ethyl 2-ethyl acetoacetate
FL/FR
heptanal cyclic ethylene acetal
FR

2-

hexen-1-ol
FL/FR

(E)-2-

hexen-1-ol
FL/FR
green
acetaldehyde butyl phenethyl acetal
FL/FR
acetaldehyde di-(Z)-3-hexen-1-yl acetal
FL/FR
acetaldehyde ethyl phenethyl acetal
FL/FR
acetaldehyde methyl hexyl acetal
FR

2-iso

butyl thiazole
FL/FR
citrus carbaldehyde / methyl anthranilate schiff's base
FR
cumin acetaldehyde
FL/FR

homo

cuminic aldehyde
FR

3,5,6-neo

cyclocitral
FR
diphenyl oxide
FL/FR
fern specialty
FR
galbanum oil
FL/FR
galbanum oil replacer
FR
galbanum oil terpeneless
FL/FR
galbanum oleoresin
FL/FR
galbascone (IFF)
FR
geranium absolute
FL/FR
green ether
FL/FR
green specialty
FR
heptyl cinnamate
FL/FR

(E)-3-

hexen-1-ol
FL/FR

(Z)-2-

hexen-1-ol
FL/FR

3-

hexen-1-ol
FL/FR

(E)-2-

hexen-1-yl acetate
FL/FR

(Z)-3-

hexen-1-yl benzoate
FL/FR

(Z)-3-

hexen-1-yl lactate
FL/FR

(Z)-3-

hexen-1-yl methyl carbonate
FL/FR

3-

hexenal
FL/FR
hexoxyacetaldehyde dimethyl acetal
FR
hexyl heptanoate
FL/FR
hyacinth absolute
FL/FR
hyacinth butanal
FR

3,6-

ivy carbaldehyde
FL/FR

2,4-

ivy carbaldehyde
FL/FR
ivy carbaldehyde
FL/FR

3,5-

ivy carbaldehyde
FL/FR

2,4-

ivy carbaldehyde / methyl anthranilate schiff's base
FR
ivy dioxolane
FR
ivy fragrance
FR

(Z)-

leaf acetal
FL/FR
leafy acetal
FL/FR
leafy oxime
FR
lilac acetaldehyde
FL/FR
marine fragrance
FR
marine specialty
FR
methyl heptine carbonate
FL/FR
narcissus flower absolute
FR

(E,Z)-2,6-

nonadien-1-yl acetate
FL/FR
octanal dimethyl acetal
FL/FR

(Z)-5-

octen-1-yl propionate
FL/FR
phenethyl acetal
FR
phenethyl tiglate
FL/FR
phenyl acetaldehyde dimethyl acetal
FL/FR
phenyl acetaldehyde ethylene glycol acetal
FR

3-

phenyl propionaldehyde
FL/FR

2-

phenyl propionaldehyde
FL/FR

iso

propyl phenyl propionaldehyde
FR

iso

propyl quinoline
FR
rosacyanthin
FR
rose leaf absolute (rosa centifolia)
FL/FR
styralyl acetate
FL/FR
triplal / ethyl anthranilate schiff's base
FR
herbal

sweet

basil absolute
FL/FR
fougere herbal fragrance
FR
herbal heptane
FR

1-(2-

methyl allyl oxy) heptane
FR
methyl ortho-anisate
FL/FR
rosemary oleoresin
FL/FR
minty

iso

pulegyl formate
FL/FR
powdery

para-

anisyl alcohol
FL/FR
waxy
allyl nonanoate
FL/FR
woody
fougere woody fragrance
FR
For Flavor
No flavor group found for these
acetaldehyde di-(Z)-3-hexen-1-yl acetal
FL/FR
allyl anthranilate
FL/FR
ethyl hydrocinnamate
FL/FR
heptyl cinnamate
FL/FR
hexanal diethyl acetal
FL/FR

3-

hexen-1-ol
FL/FR

(E)-2-

hexenal
FL

2-

hexenal
FL
hexyl heptanoate
FL/FR
hyacinth absolute
FL/FR

3,5-

ivy carbaldehyde
FL/FR
ivy carbaldehyde
FL/FR
methyl ortho-anisate
FL/FR

3-

methyl-3-pentanol
FL

2-

phenyl propyl acetate
FL/FR

(R)-2-

phenyl propyl alcohol
FL/FR

3-

phenyl propyl formate
FL/FR

3-

phenyl propyl propionate
FL/FR

iso

pulegyl formate
FL/FR
tetrahydrofurfuryl cinnamate
FL/FR
aromatic
aromatic
leafy acetal
FL/FR
chemical
styralyl alcohol
FL/FR
fatty

(Z)-3-

hexen-1-yl benzoate
FL/FR

(E)-2-

octenal
FL/FR
floral

bitter

orangeflower absolute morocco
FL/FR

bitter

orangeflower absolute tunisia
FL/FR
rose absolute (rosa damascena) bulgaria
FL/FR

laevo-

rose oxide
FL/FR
fruity

para-

anisyl alcohol
FL/FR
benzyl methyl ether
FL/FR
ethyl 2-ethyl acetoacetate
FL/FR

2-

hexen-1-ol
FL/FR
lilac acetaldehyde
FL/FR

para-

methyl benzyl acetate
FL/FR

2-

phenyl propionaldehyde dimethyl acetal
FL/FR
propyl cinnamate
FL/FR
styralyl acetate
FL/FR
green
acetaldehyde butyl phenethyl acetal
FL/FR
acetaldehyde dihexyl acetal
FL/FR
acetaldehyde ethyl phenethyl acetal
FL/FR

2-iso

butyl thiazole
FL/FR
cinnamyl alcohol
FL/FR
cumin acetaldehyde
FL/FR
diphenyl oxide
FL/FR
galbanum oil
FL/FR
galbanum oil terpeneless
FL/FR
galbanum oleoresin
FL/FR
geranium absolute
FL/FR
green ether
FL/FR

(E)-3-

hexen-1-ol
FL/FR

(Z)-2-

hexen-1-ol
FL/FR

(E)-2-

hexen-1-ol
FL/FR

(E)-2-

hexen-1-yl acetate
FL/FR

(Z)-3-

hexen-1-yl lactate
FL/FR

(Z)-3-

hexen-1-yl methyl carbonate
FL/FR

3-

hexenal
FL/FR

3,6-

ivy carbaldehyde
FL/FR

2,4-

ivy carbaldehyde
FL/FR

(Z)-

leaf acetal
FL/FR
methyl heptine carbonate
FL/FR

(E,Z)-2,6-

nonadien-1-yl acetate
FL/FR
octanal dimethyl acetal
FL/FR

(Z)-5-

octen-1-yl propionate
FL/FR
phenethyl formate
FL/FR
phenethyl tiglate
FL/FR
phenyl acetaldehyde diisobutyl acetal
FL/FR
phenyl acetaldehyde dimethyl acetal
FL/FR

2-

phenyl propionaldehyde
FL/FR

3-

phenyl propionaldehyde
FL/FR

2-

phenyl propyl alcohol
FL/FR
rose leaf absolute (rosa centifolia)
FL/FR
herbal

sweet

basil absolute
FL/FR
rosemary oleoresin
FL/FR
honey

iso

propyl phenyl acetate
FL/FR
medicinal
dimethyl benzyl carbinol
FL/FR
phenethyl salicylate
FL/FR
phenolic

para-

cresyl phenyl acetate
FL/FR
spicy

3-

phenyl propyl alcohol
FL/FR
waxy
allyl nonanoate
FL/FR

Potential Uses:

FRcortex
FRfresh outdoors
 freshener
 grass
FRhyacinth
 leaf
FRleather
FRlily of the valley

Occurrence (nature, food, other):note

Synonyms:

 acetaldehyde, 2-phenoxy-
 acetaldehyde, phenoxy-
 aldehyde cortex
 aldehyde cortex 50 (IFF)
 cortex aldehyde 50 (IFF)
 cortex aldehyde 50% benzyl alcohol (IFF)
 phenoxy acetaldehyde 50% in benzyl alcohol
 phenoxy-acetaldehyde
2-(phenoxy)acetaldehyde 50% in benzyl alcohol
 phenoxyacetaldehyde
2-phenoxyacetaldehyde 50% in benzyl alcohol

Articles:

Notes:

None found