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W213713

Sigma-Aldrich

Benzyl alcohol

greener alternative

natural, ≥98%, FG

Synonym(s):

Benzenemethanol

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About This Item

Linear Formula:
C6H5CH2OH
CAS Number:
Molecular Weight:
108.14
FEMA Number:
2137
Beilstein:
878307
EC Number:
Council of Europe no.:
58
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
2.010
NACRES:
NA.21

grade

FG
Fragrance grade
Halal
Kosher
natural

Quality Level

Agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

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

vapor density

3.7 (vs air)

vapor pressure

13.3 mmHg ( 100 °C)
3.75 mmHg ( 77 °C)

Assay

≥98%

form

liquid

autoignition temp.

817 °F

shelf life

5 yr

composition

contains IFRA restricted benzyl alcohol

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

technique(s)

UV/Vis spectroscopy: suitable

refractive index

n20/D 1.539 (lit.)

bp

203-205 °C (lit.)

mp

−16-−13 °C (lit.)

density

1.045 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

benzyl alcohol

greener alternative category

Organoleptic

fruity; floral; balsamic; sweet

SMILES string

OCc1ccccc1

InChI

1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2

InChI key

WVDDGKGOMKODPV-UHFFFAOYSA-N

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Related Categories

General description

Benzyl alcohol is an aromatic alcohol that is used as a flavoring agent and fragrance ingredient.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

Application


  • Ni-Co hexacyanoferrate hollow nanoprism with CN vacancy for electrocatalytic benzyl alcohol oxidation.: This study explores the catalytic potential of benzyl alcohol in electrochemical oxidation processes using novel nanoprism catalysts. The research highlights the efficient conversion of benzyl alcohol to benzaldehyde, providing insights into sustainable chemical synthesis and energy conversion technologies (Lv et al., 2024).

  • Combining anodic alcohol oxidative coupling for C-C bond formation with cathodic ammonia production.: This research utilizes benzyl alcohol in a dual electrocatalytic system that not only enhances C-C bond formation but also contributes to environmentally friendly ammonia production, showcasing the compound′s versatility in green chemistry applications (Xu et al., 2024).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

213.8 °F - DIN 51758

Flash Point(C)

101 °C - DIN 51758

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Burdock GA
Encyclopedia of Food and Color Additives, 1, 261-262 (1997)
Fragrance material review on anisyl alcohol
Scognamiglio J, et al.
Food And Chemical Toxicology, 50, S140-S160 (2012)
Béatrice Hechler et al.
The Journal of pharmacology and experimental therapeutics, 314(1), 232-243 (2005-03-29)
Our aim was to determine whether the newly described P2X1 antagonist NF449 [4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis(carbonylimino)))tetrakis-benzene-1,3-disulfonic acid octasodium salt] could selectively antagonize the platelet P2X1 receptor and how it affected platelet function. NF449 inhibited alpha,beta-methyleneadenosine 5'-triphosphate-induced shape change (IC50 = 83 +/- 13
Yuma Morimoto et al.
Inorganic chemistry, 51(18), 10025-10036 (2012-09-08)
The rate of oxidation of 2,5-dimethoxybenzyl alcohol (2,5-(MeO)(2)C(6)H(3)CH(2)OH) by [Fe(IV)(O)(N4Py)](2+) (N4Py = N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine) was enhanced significantly in the presence of Sc(OTf)(3) (OTf(-) = trifluoromethanesulfonate) in acetonitrile (e.g., 120-fold acceleration in the presence of Sc(3+)). Such a remarkable enhancement of the
Meenakshisundaram Sankar et al.
ACS nano, 6(8), 6600-6613 (2012-07-10)
We report a convenient excess anion modification and post-reduction step to the impregnation method which permits the reproducible preparation of supported bimetallic AuPd nanoparticles having a tight particle size distribution comparable to that found for sol-immobilization materials but without the

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