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Merck
CN

W213713

Sigma-Aldrich

苯甲醇

greener alternative

natural, ≥98%, FG

别名:

苯甲醇

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About This Item

线性分子式:
C6H5CH2OH
CAS号:
分子量:
108.14
FEMA编号:
2137
Beilstein:
878307
EC 号:
欧洲委员会编号:
58
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
2.010
NACRES:
NA.21
性状检查:
fruity; floral; balsamic; sweet
等级:
FG
Fragrance grade
Halal
Kosher
natural
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
食品过敏原:
no known allergens

等级

FG
Fragrance grade
Halal
Kosher
natural

质量水平

Agency

follows IFRA guidelines
meets purity specifications of JECFA

管理合规性

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

蒸汽密度

3.7 (vs air)

蒸汽压

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

方案

≥98%

表单

liquid

自燃温度

817 °F

保质期

5 yr

组成

contains IFRA restricted benzyl alcohol

环保替代产品特性

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

技术

UV/Vis spectroscopy: suitable

折射率

n20/D 1.539 (lit.)

沸点

203-205 °C (lit.)

mp

−16-−13 °C (lit.)

密度

1.045 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

致敏芳香化合物

benzyl alcohol

环保替代产品分类

性状检查

fruity; floral; balsamic; sweet

SMILES字符串

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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一般描述

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”.

应用


  • 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).

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

213.8 °F - DIN 51758

闪点(°C)

101 °C - DIN 51758

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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)
C L Froebe et al.
Dermatologica, 181(4), 277-283 (1990-01-01)
The relationship between the in vivo irritation potential of sodium lauryl sulfate (SLS) and linear alkyl benzene sulfonate (LAS) and the ability of these two surfactants to remove lipid from the stratum corneum (SC) in vitro were investigated. Either surfactant
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

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