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2-HYDROXY-5-NITROBENZYL BROMIDE

CAS No.
772-33-8
Chemical Name:
2-HYDROXY-5-NITROBENZYL BROMIDE
Synonyms
KOSHLAND I;KOSHLAND REAGENT;KOSHLAND'S REAGENT;KOSHLAND'S REAGENT I;Koshland's reagent 1;α-bromo-4-nitro-o-creso;α-bromo-4-nitro-o-cresol;a-Bromo-4-nitro-o-cresol;α-bromo-4-nitro-o-cresol;2-BROMOMETHYL-4-NITROPHENOL
CBNumber:
CB5229370
Molecular Formula:
C7H6BrNO3
Molecular Weight:
232.03
MDL Number:
MFCD00007340
MOL File:
772-33-8.mol
MSDS File:
SDS
Last updated:2023-06-08 17:06:38

2-HYDROXY-5-NITROBENZYL BROMIDE Properties

Melting point 144-149 °C(lit.)
Boiling point 383.0±32.0 °C(Predicted)
Density 1.795
refractive index 1.6090 (estimate)
storage temp. 2-8°C
solubility chloroform: soluble25mg/mL, clear, yellow
form Crystalline Powder
pka 6.16±0.30(Predicted)
color Beige to light brown
BRN 1868798
CAS DataBase Reference 772-33-8(CAS DataBase Reference)
FDA UNII DS4XZE4Z7T
EPA Substance Registry System Phenol, 2-(bromomethyl)-4-nitro- (772-33-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
Hazard Codes  C
Risk Statements  34
Safety Statements  26-36/37/39-45
RIDADR  UN 3261 8/PG 2
WGK Germany  3
TSCA  Yes
HazardClass  8
PackingGroup  III
HS Code  29089990
NFPA 704
0
3 0

2-HYDROXY-5-NITROBENZYL BROMIDE price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 162906 2-Hydroxy-5-nitrobenzyl bromide 90% 772-33-8 5g $68.9 2024-03-01 Buy
TCI Chemical H0601 2-Hydroxy-5-nitrobenzyl Bromide >95.0%(T) 772-33-8 5g $147 2024-03-01 Buy
TRC H950893 2-Hydroxy-5-nitrobenzyl Bromide 772-33-8 5g $45 2021-12-16 Buy
Frontier Specialty Chemicals JK247575 2-Hydroxy-5-nitrobenzyl Bromide 95% 772-33-8 5g $38 2021-12-16 Buy
American Custom Chemicals Corporation HCH0011683 2-HYDROXY-5-NITRO BENZYL BROMIDE 95.00% 772-33-8 5G $830.74 2021-12-16 Buy
Product number Packaging Price Buy
162906 5g $68.9 Buy
H0601 5g $147 Buy
H950893 5g $45 Buy
JK247575 5g $38 Buy
HCH0011683 5G $830.74 Buy

2-HYDROXY-5-NITROBENZYL BROMIDE Chemical Properties,Uses,Production

Chemical Properties

Beige to yellow crystalline powder

Uses

2-Hydroxy-5-nitrobenzyl bromide was used in covalent modification of tryptophan and tryptophan residues in monoclonal immunoglobulin. It was also used as reagent for sulfhydryl modification

Uses

Reagent for sulfhydryl modification.1

Uses

2-Hydroxy-5-nitrobenzyl bromide is a chemical reagent that reacts with and modifies chemically the tryptophan portion of protein molecules..

Synthesis Reference(s)

Journal of the American Chemical Society, 86, p. 1448, 1964 DOI: 10.1021/ja01061a045

General Description

2-Hydroxy-5-nitrobenzyl bromide is a protein modifying reagent.

Purification Methods

Crystallise the bromide from *benzene or *benzene/ligroin. It is slightly soluble in EtOH, soluble in *C6H6 and AcOH, and very soluble in ligroin. [Beilstein 6 H 367.]

7149-70-4
772-33-8
Synthesis of 2-HYDROXY-5-NITROBENZYL BROMIDE from 2-BROMO-5-NITROTOLUENE

2-HYDROXY-5-NITROBENZYL BROMIDE Suppliers

Global( 100)Suppliers
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Capot Chemical Co.,Ltd.
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Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33349 58
KOSHLAND I KOSHLAND REAGENT KOSHLAND'S REAGENT KOSHLAND'S REAGENT I ALPHA-BROMO-4-NITRO-2-CRESOL ALPHA-BROMO-4-NITRO-O-CRESOL 2-BROMOMETHYL-4-NITROPHENOL 2-HYDROXY-5-NITROBENZYL BROMIDE 2-(bromomethyl)-4-nitro-pheno o-Cresol, alpha-bromo-4-nitro- Phenol, 2-(bromomethyl)-4-nitro- α-bromo-4-nitro-o-cresol α-Bromo-4-nitro-o-cresol, 2-Bromomethyl-4-nitrophenol, Koshland I, Koshlands Reagent I a-Bromo-4-nitro-o-cresol a-Bromo-4-nitro-o-methylphenol BETA-1-BROMO-4-NITRO-O-CRESOL 2-Hydroxy-5-nitrobenzyl bromide ,95% 2-Hydroxy-5-nitrobenzyl bromide,α-Bromo-4-nitro-o-cresol, 2-Bromomethyl-4-nitrophenol, Koshland I, Koshland’s Reagent I alpha-Bromo-4-nitro-o-cresol Koshland's Reagent 2-Hydroxy-5-nitrobenzyl bromide 90% Koshland's reagent 1 alpha-Bromo-4-nitro-o-cresol,95% alpha-Bromo-4-nitro-o-cresol,98% 2-Hydroxy-5-nitrobenzylBromide> α-bromo-4-nitro-o-cresol α-bromo-4-nitro-o-creso 772-33-8 73-1 HOC6H3NO2CH2Br Building Blocks BioChemical Organic Building Blocks Proteomics and Protein Expression Protein Modification Proteomics Reagents for tryptophan modification Oxygen Compounds Phenols Specific Amino Acid Modification Building Blocks C6 to C8 Chemical Synthesis Organic Building Blocks Oxygen Compounds Phenols