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Y0000167

Alcohol bencílico

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

Bencenometanol

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About This Item

Fórmula lineal:
C6H5CH2OH
Número de CAS:
100-51-6
Peso molecular:
108.14
Beilstein/REAXYS Number:
878307
MDL number:
MFCD00004599
UNSPSC Code:
41116107
PubChem Substance ID:
329830870
NACRES:
NA.24

grade

pharmaceutical primary standard

agency

EP Reference Standard

vapor density

3.7 (vs air)

vapor pressure

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

API family

benzalkonium chloride

autoignition temp.

817 °F

manufacturer/tradename

EDQM

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)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

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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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

application

Benzyl alcohol EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

213.8 °F - DIN 51758

flash_point_c

101 °C - DIN 51758

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Certificados de análisis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

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Sigma-Aldrich

12392

Benzyl benzoate

Alcohol bencílico ACS reagent, ≥99.0%

Sigma-Aldrich

402834

Alcohol bencílico

Alcohol bencílico ≥99%, FCC, FG

Sigma-Aldrich

W213705

Alcohol bencílico

Jian Zhu et al.
Journal of the American Chemical Society, 135(12), 4719-4721 (2013-03-19)
We describe the use of benzyl alcohols in a solvothermal/alcoholysis reaction to form nanocrystalline sheets of anatase titania. By tuning the reaction conditions, we adjust the size of the nanosheets. The type and density of benzyl groups that decorate the
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
Luis E Santos-Figueroa et al.
Chemical Society reviews, 42(8), 3489-3613 (2013-02-13)
This review focuses on examples reported in the years 2010-2011 dealing with the design of chromogenic and fluorogenic chemosensors or reagents for anions.
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