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About This Item
Linear Formula:
O2NC6H4CH2OH
CAS Number:
Molecular Weight:
153.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-588-2
Beilstein/REAXYS Number:
2044769
MDL number:
Assay:
98%
InChI key
CWNPOQFCIIFQDM-UHFFFAOYSA-N
InChI
1S/C7H7NO3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4,9H,5H2
SMILES string
OCc1cccc(c1)[N+]([O-])=O
assay
98%
bp
175-180 °C/3 mmHg (lit.)
Quality Level
density
1.29 g/mL at 20 °C (lit.)
functional group
hydroxyl, nitro
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General description
3-Nitrobenzyl alcohol is the best substrate for cytosolic alcohol dehydrogenase.
Application
3-Nitrobenzyl alcohol was employed as matrix during fast-atom bombardment mass spectrometry. It was used in isolation of palmitylated peptide fragment from bovine rhodopsin and its characterization by mass spectrometry.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Charlotte Mallet et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(21), 7944-7953 (2015-04-14)
A series of 2,5-distyrylfuran derivatives bearing pentafluorophenyl- and cyanovinyl units have been synthesized for aggregation-induced emission (AIE). The effect of the type and extent of the supramolecular connections on the AIE of the furan derivatives were examined and correlated with
Frank Kjeldsen et al.
Analytical chemistry, 79(24), 9243-9252 (2007-11-21)
We have tested the effect of m-nitrobenzyl alcohol (m-NBA) as a method to increase the average charge state of protonated gas-phase molecular ions generated by ESI from tryptic peptides and phosphopeptides. Various concentrations of m-NBA were added to the mobile
Harry J Sterling et al.
Journal of the American Society for Mass Spectrometry, 20(10), 1933-1943 (2009-08-18)
The use of m-nitrobenzyl alcohol (m-NBA) to enhance charging of noncovalent complexes formed by electrospray ionization from aqueous solutions was investigated. Addition of up to 1% m-NBA can result in a significant increase in the average charging of complexes, ranging
D I Papac et al.
The Journal of biological chemistry, 267(24), 16889-16894 (1992-08-25)
Bovine rhodopsin has been reported to be S-palmitylated at cysteines 322 and 323 (Ovchinnikov, Y. A., Abdulaev, N. G., and Bogachuk, A.S. (1988) FEBS Lett. 230, 1-5). Using a combination of enzymatic and chemical cleavage techniques in conjunction with tandem
Shirley H Lomeli et al.
Journal of the American Society for Mass Spectrometry, 20(4), 593-596 (2008-12-23)
Increased multiple charging of native proteins and noncovalent protein complexes is observed in electrospray ionization (ESI) mass spectra obtained from nondenaturing protein solutions containing up to 1% (vol/vol) m-nitrobenzyl alcohol (m-NBA). The increases in charge ranged from 8% for the
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