146056
3-Nitrobenzyl alcohol
98%
Synonym(s):
NOBA
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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%
mp
26-32 °C (lit.)
density
1.29 g/mL at 20 °C (lit.)
functional group
hydroxyl, nitro
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
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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
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
Yuya Domoto et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(48), 15998-16005 (2014-10-07)
Efficient end-capping synthesis of neutral donor-acceptor (D-A) [2]rotaxanes without loading any catalysts or activating agents was achieved by utilizing high reactivity of a pentacoordinated hydrosilane toward salicylic acid derivatives. As components of [2]rotaxanes, an electron-deficient naphthalenediimide-containing axle with a salicylic
R S Pappas et al.
Carbohydrate research, 197, 1-14 (1990-03-25)
A derivatization method, adapted from that of Angel et al. (ref. 10), for sequencing sugar residues in partially degraded poly- and oligo-saccharides using positive-ion f.a.b.-m.s. is described. Derivative selection provides sequence information by directing fragmentation exclusively to both sides of
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