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Key Documents

146056

Sigma-Aldrich

3-Nitrobenzyl alcohol

98%

Synonym(s):

NOBA

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About This Item

Linear Formula:
O2NC6H4CH2OH
CAS Number:
Molecular Weight:
153.14
Beilstein:
2044769
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

bp

175-180 °C/3 mmHg (lit.)

mp

26-32 °C (lit.)

density

1.29 g/mL at 20 °C (lit.)

functional group

hydroxyl
nitro

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

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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
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
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
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
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

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