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Merck

W246808

Isoeugenol

mixture of cis and trans, 99%, FG

Sinónimos:

2-Methoxy-4-propenylphenol

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Fórmula lineal:
CH3OC6H3(CH=CHCH3)OH
Número CAS:
97-54-1
Peso molecular:
164.20
FEMA Number:
2468
Council of Europe no.:
172
UNSPSC Code:
12164502
PubChem Substance ID:
24901116
Flavis number:
4.004
EC Number:
202-590-7
NACRES:
NA.21
MDL number:
MFCD00009285
Beilstein/REAXYS Number:
1909602
Organoleptic:
clove; woody; spicy; sweet
Grade:
FG, Halal, Kosher
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens

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SMILES string

OC1=CC=C(/C=C/C)C=C1OC

InChI

1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3-7,11H,1-2H3/b4-3+

InChI key

BJIOGJUNALELMI-ONEGZZNKSA-N

biological source

synthetic

grade

FG, Halal, Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002, FDA 21 CFR 117, FDA 21 CFR 172.515

vapor density

>1 (vs air)

vapor pressure

<0.01 mmHg ( 20 °C)

assay

99%

refractive index

n20/D 1.575 (lit.)

bp

132 °C/10 mmHg (lit.)

density

1.082 g/mL at 25 °C

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

clove; woody; spicy; sweet

Quality Level

300, 400

Gene Information

rat ... Ar(24208)

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1A - STOT SE 3

target_organs

Respiratory system

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 2

flash_point_f

233.6 °F - closed cup

flash_point_c

112 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
SHBS8944
SHBP2691
SHBP9442
SHBN6662
SHBM1335

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Gurpreet Kaur et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50(8), 2689-2695 (2012-05-23)
Isoeugenol, a component of clover oil, possesses potent anti-inflammatory and antioxidant activity. In the present study, we investigated the effect on experimentally induced adjuvant arthritis in rats. Induction of arthritis in adjuvant exposed rats was confirmed by appearance of several
J Krupa et al.
The journal of physical chemistry. B, 116(36), 11148-11158 (2012-07-26)
In situ photochemical transformations of monomers of 2-methoxy-4-(prop-1-enyl)phenol (isoeugenol) and 2-methoxy-4-(prop-2-enyl)phenol (eugenol) isolated in low temperature matrices were induced by tunable UV laser light, and the progress of the reactions was followed by FTIR spectroscopy. Conformer-selective E ↔ Z geometrical
Aurélie Frankart et al.
Archives of dermatological research, 304(4), 289-303 (2012-01-25)
Models of reconstructed human epidermis (RHE) holding proliferating and fully differentiated cultured keratinocytes allow in vitro investigation of early molecular and cellular epidermal events during the complex response of keratinocytes at the onset of allergic contact dermatitis (ACD) or sensitization.
Michaela Kalmes et al.
Journal of toxicology and environmental health. Part A, 75(8-10), 478-491 (2012-06-13)
The phenolic derivatives eugenol and isoeugenol, which are naturally found in essential oils of different spices, are commonly used as fragrances. Recently data demonstrated that growth suppression produced by these substances occurs in keratinocytes and that the effects may be
Charlotte Menné Bonefeld et al.
Contact dermatitis, 65(6), 336-342 (2011-07-20)
Perfumes are complex mixtures composed of many fragrance ingredients, many of which are known to be only weak allergens when tested individually. It is therefore surprising that fragrance contact allergy is one of the most common forms of contact allergy.
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