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Assay
98%
bp
175-180 °C/3 mmHg (lit.)
mp
26-32 °C (lit.)
density
1.29 g/mL at 20 °C (lit.)
SMILES string
OCc1cccc(c1)[N+]([O-])=O
InChI
1S/C7H7NO3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4,9H,5H2
InChI key
CWNPOQFCIIFQDM-UHFFFAOYSA-N
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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 Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
233.6 °F - closed cup
Flash Point(C)
112 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
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
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
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
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