H21101
4-Hydroxyphenylacetonitrile
98%
Synonym(s):
4-Hydroxybenzyl cyanide
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
HOC6H4CH2CN
CAS Number:
Molecular Weight:
133.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
238-046-0
Beilstein/REAXYS Number:
1934470
MDL number:
Product Name
4-Hydroxyphenylacetonitrile, 98%
InChI
1S/C8H7NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5H2
InChI key
AYKYOOPFBCOXSL-UHFFFAOYSA-N
SMILES string
Oc1ccc(CC#N)cc1
assay
98%
bp
330 °C/756 mmHg (lit.)
mp
67-70 °C (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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.
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
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
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
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service