402834
Benzyl alcohol
ACS reagent, ≥99.0%
동의어(들):
Benzenemethanol
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5CH2OH
CAS 번호:
Molecular Weight:
108.14
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39023110
UNSPSC Code:
12352104
EC Number:
202-859-9
MDL number:
Beilstein/REAXYS Number:
878307
Assay:
≥99.0%
Grade:
ACS reagent
Bp:
203-205 °C (lit.)
Vapor pressure:
13.3 mmHg ( 100 °C), 3.75 mmHg ( 77 °C)
InChI key
WVDDGKGOMKODPV-UHFFFAOYSA-N
InChI
1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2
SMILES string
OCc1ccccc1
grade
ACS reagent
vapor density
3.7 (vs air)
vapor pressure
13.3 mmHg ( 100 °C), 3.75 mmHg ( 77 °C)
assay
≥99.0%
form
liquid
autoignition temp.
817 °F
expl. lim.
0.34-6.3 %
dilution
(for analytical testing)
impurities
≤0.01% Benzaldehyde (C6H5CHO), ≤0.02% Acetophenone (C6H5COCH3)
ign. residue
≤0.005%
color
APHA: ≤20
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.)
Quality Level
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General description
Benzyl alcohol (BnOH) is a monoaromatic primary alcohol widely used as a solvent and an intermediate in cosmetic formulations, pharmaceutical and flavor/fragrance industries. Commercial method for its synthesis is by the alkaline hydrolysis of benzyl chloride. Conformational studies by ab initio calculations shows gauche cis conformation around the alcoholic group.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Application
Benzyl alcohol may be used for the benzylation of toluene.
signalword
Warning
hcodes
저장 등급
10 - Combustible liquids
flash_point_f
213.8 °F - DIN 51758
flash_point_c
101 °C - DIN 51758
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1B
Engineering Escherichia coli for renewable benzyl alcohol production.
Pugh S, et al.
Metabolic Engineering Communications, 2, 39-45 (2015)
The most stable conformer of benzyl alcohol.
Miller BJ, et al.
Chemical Physics Letters, 466(1), 21-26 (2008)
Application of statistical design to benzylation of toluene with benzyl alcohol.
Alam A, et al.
Chemical Engineering & Technology, 31(3), 417-420 (2008)
Po-Yu Liao et al.
Frontiers in neuroanatomy, 14, 559402-559402 (2020-11-17)
Oxytocin, a neuropeptide and peptide hormone, is produced by neurons in the hypothalamus and released by the posterior pituitary to control breastfeeding and labor. Recent studies have revealed that oxytocin in the central nervous system is also involved in modulating
Poincyane Assis-Nascimento et al.
Journal of neuroscience methods, 263, 57-67 (2016-02-09)
Traumatic brain injury (TBI) continues to be a major source of death and disability worldwide, and one of the earliest and most profound deficits comes from vascular damage and breakdown of the blood-brain barrier (BBB). Cerebral vascular endothelial cells (cvECs)
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