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W268518

Sigma-Aldrich

α-Methylbenzyl alcohol

≥99%, FCC, FG

Synonyme(s) :

(±)-1-Phenylethanol, (±)-α-Methylbenzyl alcohol, Methyl phenyl carbinol, Styrallyl alcohol, Styrene alcohol

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About This Item

Formule linéaire :
C6H5CH(OH)CH3
Numéro CAS:
Poids moléculaire :
122.16
Numéro FEMA:
2685
Numéro Beilstein :
1905149
Numéro CE :
Conseil de l'Europe Nº :
2030
Numéro MDL:
Code UNSPSC :
12164502
ID de substance PubChem :
Numéro Flavis :
2.064
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

Qualité

FG
Halal
Kosher

Agence

meets purity specifications of JECFA

Conformité réglementaire

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

Densité de vapeur

4.21 (vs air)

Pression de vapeur

0.1 mmHg ( 20 °C)

Pureté

≥99%

Indice de réfraction

n20/D 1.527 (lit.)

Point d'ébullition

204 °C/745 mmHg (lit.)

Pf

19-20 °C (lit.)

Densité

1.012 g/mL at 25 °C (lit.)

Application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

Allergène alimentaire

no known allergens

Propriétés organoleptiques

medicinal; chemical; sweet

Chaîne SMILES 

CC(O)c1ccccc1

InChI

1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3

Clé InChI

WAPNOHKVXSQRPX-UHFFFAOYSA-N

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Application


  • Update to RIFM fragrance ingredient safety assessment,a-methylbenzyl alcohol, CAS registry number 98-85-1.: This study updates the safety assessment of a-methylbenzyl alcohol, focusing on its use as a fragrance ingredient. The research addresses toxicological data and regulatory compliance, ensuring the compound′s safe application in consumer products (Api et al., 2024).

  • Characterization of the Key Aroma Compounds of Three Kinds of Chinese Representative Black Tea and Elucidation of the Perceptual Interactions of Methyl Salicylate and Floral Odorants.: This study identifies the key aroma compounds in Chinese black tea, including a-methylbenzyl alcohol. The research provides insights into the sensory properties and potential applications in flavor and fragrance industries (Niu et al., 2022).

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Eye Irrit. 2

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

187.9 °F - Pensky-Martens closed cup

Point d'éclair (°C)

86.6 °C - Pensky-Martens closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificats d'analyse (COA)

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Henry Gruen et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(11), 1344-1352 (2008-10-30)
The photoreactions of 1-nitro-9,10-anthraquinone (N1) and 2-methyl-1-nitro-9,10-anthraquinone (N2) were studied in benzene and acetonitrile in the presence of 1-phenylethanol. For N2, a short-lived 10 ns transient observed upon flash photolysis is attributed to a triplet state, which can be intercepted
Binbin Zhang et al.
ChemSusChem, 5(12), 2469-2473 (2012-10-24)
Exploration of new and effective routes to conduct organic reactions in water using the special properties of water/organics is of great importance. In this work, we performed the disproportionation of various aromatic alcohols in water and in different organic solvents.
Pedro Lozano et al.
Biotechnology letters, 28(19), 1559-1565 (2006-08-11)
Continuous dynamic kinetic resolution processes in different ionic liquid/supercritical carbon dioxide biphasic systems were carried out by simultaneously using both immobilized Candida antarctica lipase B (Novozym 435) and silica modified with benzenosulfonic acid (SCX) catalysts at 40 degrees C and
Directed evolution of galactose oxidase: generation of enantioselective secondary alcohol oxidases.
Franck Escalettes et al.
Chembiochem : a European journal of chemical biology, 9(6), 857-860 (2008-03-12)
Galia Maayan et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(33), 13679-13684 (2009-08-12)
Many naturally occurring biopolymers (i.e., proteins, RNA, DNA) owe their unique properties to their well-defined three-dimensional structures. These attributes have inspired the design and synthesis of folded architectures with functions ranging from molecular recognition to asymmetric catalysis. Among these are

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