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W246808

Sigma-Aldrich

Isoeugenol

mixture of cis and trans, 99%, FG

Synonym(e):

2-Methoxy-4-propenyl-phenol

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About This Item

Lineare Formel:
CH3OC6H3(CH=CHCH3)OH
CAS-Nummer:
97-54-1
Molekulargewicht:
164.20
FEMA-Nummer:
2468
Beilstein:
1909602
EG-Nummer:
202-590-7
CoE-Nummer:
172
MDL-Nummer:
MFCD00009285
UNSPSC-Code:
12164502
PubChem Substanz-ID:
24901116
Flavis-Nummer:
4.004
NACRES:
NA.21

Biologische Quelle

synthetic

Qualitätsniveau

400

Qualität

FG
Halal
Kosher

Agentur

meets purity specifications of JECFA

Einhaltung gesetzlicher Vorschriften

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

Dampfdichte

>1 (vs air)

Dampfdruck

<0.01 mmHg ( 20 °C)

Assay

99%

Brechungsindex

n20/D 1.575 (lit.)

bp

132 °C/10 mmHg (lit.)

Dichte

1.082 g/mL at 25 °C

Anwendung(en)

flavors and fragrances

Dokumentation

see Safety & Documentation for available documents

Nahrungsmittelallergen

no known allergens

Organoleptisch

clove; woody; spicy; sweet

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+

InChIKey

BJIOGJUNALELMI-ONEGZZNKSA-N

Angaben zum Gen

rat ... Ar(24208)

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Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

233.6 °F - closed cup

Flammpunkt (°C)

112 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
SHBP2691
SHBP9442
SHBN6662
SHBM1335
SHBL7529

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Die Dokumentenbibliothek aufrufen

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
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
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.
Jakob Torp Madsen et al.
Cutaneous and ocular toxicology, 30(2), 116-123 (2011-01-05)
Attempts to improve formulation of topical products are a continuing process and the development of micro- and nanovesicular systems as well as polymeric microparticles has led to marketing of topical drugs and cosmetics using these technologies. Encapsulation of some well-known
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