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4-AZIDOPHENACYL BROMIDE

Basic information Safety Supplier Related

4-AZIDOPHENACYL BROMIDE Basic information

Product Name:
4-AZIDOPHENACYL BROMIDE
Synonyms:
  • 4-Azidophenacyl bromide powder
  • P-AZIDOPHENACYL BROMIDE
  • 4-AZIDOPHENACYL BROMIDE
  • 1-(4-Azidophenyl)-2-bromo-ethanone
  • 4μ-Azido-2-bromoacetophenone, 4-Azido-α-bromoacetophenone
  • 4'-Azido-α-bromoacetophenone
  • 1-(4-Azidophenyl)-2-bromoethan-1-one, 4-(Bromoacetyl)phenyl azide
  • 1-(4-azidophenyl)-2-bromoethan-1-one
CAS:
57018-46-9
MF:
C8H6BrN3O
MW:
240.06
EINECS:
260-519-5
Product Categories:
  • Affinity Chromatography
  • Photoaffinity Labels
  • Aromatics
  • MTS & Sulfhydryl Active Reagents
  • Sulfur & Selenium Compounds
Mol File:
57018-46-9.mol
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4-AZIDOPHENACYL BROMIDE Chemical Properties

Melting point:
64-65 °C
storage temp. 
2-8°C
solubility 
methanol: 50 mg/mL
form 
powder
color 
yellow
BRN 
1961705
Stability:
Light, Temperature And Moisture Sensitive, Temperature and Moisture sensitive
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Safety Information

Hazard Codes 
F,C
Risk Statements 
11-34-42/43
Safety Statements 
16-26-27-36/37/39-45
RIDADR 
UN 1325 4.1/PG 2
WGK Germany 
3
4.5-8-10-19
HazardClass 
4.1
PackingGroup 
III
HS Code 
29299090

MSDS

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4-AZIDOPHENACYL BROMIDE Usage And Synthesis

Chemical Properties

4-AZIDOPHENACYL BROMIDE is off-White Crystalline Solid

Uses

4-AZIDOPHENACYL BROMIDE is a versatile photolabile bifunctional reagent. Useful for investigating the active sites of sulfhydryl enzymes-particularly those which posess a particularly reactive cysteine residue at the active site. Used to study the nature of the ribosomal binding site of E. coli tRNAVal.

Uses

Photoactive, heterobifunctional cross-linking reagent. Typically, the initial reaction couples to sulfhydryl in the pH range 7.0-8.0. Second bonding occurs during UV irradiation (250 nm) via reactive nitrene. The latter bonding is rapid and non-specific.

4-AZIDOPHENACYL BROMIDESupplier

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