73148
3-Nitrobenzyl alcohol
suitable for mass spectrometry (MS), ≥99.5%
Synonym(s):
NOBA
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Quality Level
Assay
≥99.5% (GC)
≥99.5%
form
(Powder or Crystals or Solid or Liquid)
technique(s)
H-NMR: suitable
mass spectrometry (MS): suitable
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 (3-NBA) is most commonly used matrix for spectrometry methods. It helps in the analysis of porphyrins, cyclic peptides, alkali metal cationized fatty acids for collisional activation and also certain organoruthenium compounds.
Application
3-NBA has been used as liquid matrix in Ionization in liquid secondary ion mass spectrometry.
Other Notes
Matrix used in fast atom bombardment 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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Org. Mass Spectrom., 19, 581-581 (1984)
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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
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
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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
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