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Key Documents

W247006

Sigma-Aldrich

Isoeugenyl acetate

≥98%, FCC, FG

Synonym(s):

NSC 46121

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About This Item

Empirical Formula (Hill Notation):
C12H14O3
CAS Number:
Molecular Weight:
206.24
FEMA Number:
2470
EC Number:
Council of Europe no.:
220
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.030
NACRES:
NA.21
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biological source

synthetic

Quality Level

grade

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 172.515

Assay

≥98%

composition

contains IFRA restricted Isoeugenol

mp

79-81 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

isoeugenol

Organoleptic

carnation; floral; spicy; sweet

SMILES string

COc1cc(\C=C\C)ccc1OC(C)=O

InChI

1S/C12H14O3/c1-4-5-10-6-7-11(15-9(2)13)12(8-10)14-3/h4-8H,1-3H3/b5-4+

InChI key

IUSBVFZKQJGVEP-SNAWJCMRSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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I R White et al.
Contact dermatitis, 41(5), 272-275 (1999-12-20)
The prevalence of contact allergy to the fragrance mix in individuals with eczema is up to 10%. Within the mix, isoeugenol (CAS 97-54-1) is an important individual allergen. Until May 1998, the IFRA (International Fragrance Association) guidelines suggested that isoeugenol
Suresh Chandra Rastogi et al.
Contact dermatitis, 58(5), 278-281 (2008-04-18)
Isoeugenol, an important fragrance allergen in consumers, has been restricted to 200 p.p.m. since 1998 according to guidelines issued by the fragrance industry. However, no decline in contact allergy to isoeugnol has been detected. It has been speculated that isoeugenol
Fragrance allergen substitution.
J Middleton
Contact dermatitis, 42(4), 249-249 (2000-04-06)
R ten Have et al.
The Biochemical journal, 347(Pt 2), 585-591 (2000-04-06)
Lignin peroxidase (LiP) has been used to study the C(alpha)-C(beta) cleavage of the propylene side chain in 1-(3',4'-dimethoxyphenyl)propene (DMPP) to 3,4-dimethoxybenzaldehyde (veratraldehyde, VAD). Under an air atmosphere, LiP oxidized DMPP to VAD (27.8%) and 1-(3',4'-dimethoxyphenyl)propan-2-one (DMPA, 8.7%), after 10 min
S Tanaka et al.
Contact dermatitis, 51(5-6), 288-291 (2004-12-21)
A total of 2261 (808 male, 1453 female) consecutive patients attending contact dermatitis clinics were patch tested to isoeugenol and its derivatives listed in the EU Inventory of Fragrance Ingredients. Positive reactions were found to isoeugenol in 40, transisoeugenol in

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