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Merck
모든 사진(2)

Key Documents

H21101

Sigma-Aldrich

4-Hydroxyphenylacetonitrile

98%

동의어(들):

4-Hydroxybenzyl cyanide

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About This Item

Linear Formula:
HOC6H4CH2CN
CAS Number:
Molecular Weight:
133.15
Beilstein:
1934470
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

bp

330 °C/756 mmHg (lit.)

mp

67-70 °C (lit.)

SMILES string

Oc1ccc(CC#N)cc1

InChI

1S/C8H7NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5H2

InChI key

AYKYOOPFBCOXSL-UHFFFAOYSA-N

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픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

S Buskov et al.
Journal of biochemical and biophysical methods, 43(1-3), 157-174 (2000-06-28)
In the present study analytical and preparative supercritical fluid chromatography (SFC) were used for investigation of myrosinase catalysed degradation of 4-hydroxybenzylglucosinolate (sinalbin). Sinalbin occurs as a major glucosinolate in seeds of Sinapis alba L., in various mustards and other food
L B Willis et al.
Canadian journal of microbiology, 44(6), 554-564 (1998-09-12)
Defined insertion mutations have been constructed in the Rhizobium (Sinorhizobium) meliloti phbC gene, which encodes poly-beta-hydroxybutyrate (PHB) synthase. The locus was isolated and subcloned from a genomic library of R. meliloti Rm1021 by complementation of phbC mutation of Alcaligenes eutrophus.
C J Cooksey et al.
The Biochemical journal, 333 ( Pt 3), 685-691 (1998-07-25)
When 3,4-dihydroxybenzylcyanide (DBC) is oxidized by mushroom tyrosinase, the first visible product, identified as the corresponding quinomethane, exhibits an absorption maximum at 480 nm. Pulse-radiolysis experiments, in which the o-quinone is formed by disproportionation of semiquinone radicals generated by single-electron
J M Baldoni et al.
The Journal of biological chemistry, 255(19), 8987-8990 (1980-10-10)
Dopamine beta-hydroxylase (EC 1.14.17.1) is inactivated by p-hydroxybenzylcyanide (PHBC) in a manner characteristic of a suicide substrate. The inactivation 1) is first order in inhibitor (Kd = 1.9 mM, k2 = 0.05 min-1, pH 5.0), 2) exhibits saturation kinetics, and
G Colombo et al.
The Journal of biological chemistry, 259(3), 1607-1615 (1984-02-10)
Dopamine beta-hydroxylase was incubated with p-hydroxybenzyl cyanide, ascorbate, and O2 and the products of the hydroxylation reaction were monitored by high performance liquid chromatography. At early times, p-hydroxymandelonitrile was the sole product but this compound slowly decomposed to p-hydroxybenzaldehyde and

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