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W213713

Sigma-Aldrich

Alcool benzilico

greener alternative

natural, ≥98%, FG

Sinonimo/i:

Benzenmetanolo

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About This Item

Formula condensata:
C6H5CH2OH
Numero CAS:
Peso molecolare:
108.14
Numero FEMA:
2137
Beilstein:
878307
Numero CE:
N° CoE:
58
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
2.010
NACRES:
NA.21

Grado

FG
Fragrance grade
Halal
Kosher
natural

Livello qualitativo

agenzia

follows IFRA guidelines
meets purity specifications of JECFA

Conformità normativa

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

Densità del vapore

3.7 (vs air)

Tensione di vapore

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

Saggio

≥98%

Forma fisica

liquid

Temp. autoaccensione

817 °F

Durata

5 yr

Composizione

contains IFRA restricted benzyl alcohol

Caratteristiche più verdi

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

tecniche

UV/Vis spectroscopy: suitable

Indice di rifrazione

n20/D 1.539 (lit.)

P. eboll.

203-205 °C (lit.)

Punto di fusione

−16-−13 °C (lit.)

Densità

1.045 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

benzyl alcohol

Categoria alternativa più verde

Organolettico

fruity; floral; balsamic; sweet

Stringa SMILE

OCc1ccccc1

InChI

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

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Categorie correlate

Descrizione generale

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”.

Applicazioni


  • 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).

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

213.8 °F - DIN 51758

Punto d’infiammabilità (°C)

101 °C - DIN 51758

Dispositivi di protezione individuale

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


Certificati d'analisi (COA)

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Encyclopedia of Food and Color Additives, 1, 261-262 (1997)
Fragrance material review on anisyl alcohol
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Food And Chemical Toxicology, 50, S140-S160 (2012)
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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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