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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
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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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The effects of aqueous solution supercharging on the solution- and gas-phase structures of two protein complexes were investigated using traveling-wave ion mobility-mass spectrometry (TWIMS-MS). Low initial concentrations of m-nitrobenzyl alcohol (m-NBA) in the electrospray ionization (ESI) solution can effectively increase
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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
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