Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

3-Nitrobenzyl alcohol

From Wikipedia, the free encyclopedia
3-Nitrobenzyl alcohol
Names
Preferred IUPAC name
(3-Nitrophenyl)methanol
Other names
m-Nitrobenzyl alcohol
Benzyl alcohol,m-nitro
3-Nitrobenzyl alcohol
Benzenemethanol, 3-nitro-
3-Nitrobenzenemethanol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.009.627Edit this at Wikidata
UNII
  • InChI=1S/C7H7NO3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4,9H,5H2 checkY
    Key: CWNPOQFCIIFQDM-UHFFFAOYSA-N checkY
  • InChI=1/C7H7NO3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4,9H,5H2
    Key: CWNPOQFCIIFQDM-UHFFFAOYAE
  • C1=CC(=CC(=C1)[N+](=O)[O-])CO
  • [O-][N+](=O)c1cccc(c1)CO
Properties
C7H7NO3
Molar mass153.135
Density1.29 g/mL
Melting point30 to 32 °C (86 to 90 °F; 303 to 305 K)
Boiling point175 to 180 °C (347 to 356 °F; 448 to 453 K) (3 mmHg)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

The compound3-nitrobenzyl alcohol is anorganic compound with the formula C7H7NO3.

Desorption mass spectrometry matrix

[edit]

Inmass spectrometry this compound is often abbreviated as "3-NBA" or "m-NBA." It has been used as a liquid matrix forfast atom bombardment[1] andmatrix-assisted laser desorption ionization.[2][3] Inelectrospray ionization 3-NBA is doped into low surface tension spray solvents to increase analyte charging.[4]

References

[edit]
  1. ^Meili, J.; Seibl, J. (1984), "A new versatile matrix for fast atom bombardment analysis",Org. Mass Spectrom.,19 (11): 581,doi:10.1002/oms.1210191111
  2. ^Zhao, Shankai; Somayajula, Kasi V.; Sharkey, Andrew G.; Hercules, David M.; Hillenkamp, Franz.; Karas, Michael.; Ingendoh, Arndt. (1991), "Novel method for matrix-assisted laser mass spectrometry of proteins",Anal. Chem.,63 (5): 450,doi:10.1021/ac00005a012
  3. ^Chan, T. W. Dominic (1992), "Matrix-assisted laser desorption/ionization using a liquid matrix: Formation of high-mass cluster ions from proteins",Org. Mass Spectrom.,27 (1):53–56,doi:10.1002/oms.1210270114
  4. ^Anthony T. Iavarone and Evan R. Williams (2003), "Mechanism of Charging and Supercharging Molecules in Electrospray Ionization",J. Am. Chem. Soc.,125 (8):2319–2327,doi:10.1021/ja021202t,PMC 1343448,PMID 12590562
By consumption
Alcohols found in
alcoholic drinks
Medical alcohol
Toxic alcohols
Primary
alcohols
(1°)
Methanol
Ethanol
Butanol
Straight-chain
saturated
C1 — C9
Straight-chain
saturated
C10 — C19
Straight-chain
saturated
C20 — C29
Straight-chain
saturated
C30 — C39
Straight-chain
saturated
C40 — C49
Secondary
alcohols (2°)
Tertiary
alcohols (3°)
Hydric alcohols
Monohydric alcohols
Dihydric alcohols
Trihydric alcohols
Polyhydric alcohols (sugar alcohols)
Amyl alcohols
Aromatic alcohols
Saturated
fatty alcohols
Branched and
unsaturated
fatty alcohols
Sugar alcohols
C1 — C7
Deoxy sugar
alcohols
Cyclic sugar
alcohols
Glycylglycitols
Terpene alcohols
Monoterpene
alcohols
Sesquiterpene
alcohols
Diterpene
alcohols
Dialcohols
Trialcohols
Sterols
Fluoroalcohols
Preparations
Reactions
Retrieved from "https://en.wikipedia.org/w/index.php?title=3-Nitrobenzyl_alcohol&oldid=1201496514"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp