ChemicalBook > CAS DataBase List > OXALYL BROMIDE

OXALYL BROMIDE

Product Name
OXALYL BROMIDE
CAS No.
15219-34-8
Chemical Name
OXALYL BROMIDE
Synonyms
OB;Oxalyl dibromide;LEPD;CAD11;CDHOB;BrCOCOBr;NSC 96957;OXALYL BROMO;Oxaly bromide;Oxayl Bromide
CBNumber
CB0762939
Molecular Formula
C2Br2O2
Formula Weight
215.83
MOL File
15219-34-8.mol
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OXALYL BROMIDE Property

Melting point:
-19 °C (lit.)
Boiling point:
16-17 °C/10 mmHg (lit.)
Density 
1.517 g/mL at 25 °C
refractive index 
n20/D 1.522(lit.)
Flash point:
-19°C
storage temp. 
2-8°C
solubility 
Benzene (Slightly), Chloroform
form 
Liquid
color 
Clear
biological source
goat
BRN 
1744437
Stability:
Moisture Sensitive
InChI
InChI=1S/C2Br2O2/c3-1(5)2(4)6
InChIKey
JAZLVNXWYDFQFE-UHFFFAOYSA-N
SMILES
C(Br)(=O)C(Br)=O
CAS DataBase Reference
15219-34-8
EPA Substance Registry System
Ethanedioyl dibromide (15219-34-8)
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Safety

Hazard Codes 
C,T
Risk Statements 
23/24/25-34-40-29-20-14-37
Safety Statements 
26-36/37/39-45-28-27
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
8-9
HazardClass 
8
PackingGroup 
II
HS Code 
29171990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

H332Harmful if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SAB2501745
Product name
Anti-CDH11 antibody produced in goat
Purity
affinity isolated antibody, buffered aqueous solution
Packaging
100μg
Price
$586
Updated
2025/07/31
Sigma-Aldrich
Product number
L5037
Product name
Leptin from rat
Purity
≥97% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder
Packaging
1MG
Price
$213.5
Updated
2025/07/31
Sigma-Aldrich
Product number
113034
Product name
Oxalyl bromide
Purity
97%
Packaging
25g
Price
$203
Updated
2025/07/31
Sigma-Aldrich
Product number
113034
Product name
Oxalyl bromide
Purity
97%
Packaging
100g
Price
$338
Updated
2025/07/31
Sigma-Aldrich
Product number
323233
Product name
Oxalyl bromide solution
Purity
2.0 M in methylene chloride
Packaging
50ml
Price
$224
Updated
2025/07/31
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OXALYL BROMIDE Chemical Properties,Usage,Production

Chemical Properties

clear yellow to yellow-green liquid

Uses

Used in synthetic applications of carbon-substituted iminium salts
Reactant for:
Synthesis of mutasynthons added to cultures of A. pretiosum for mutasynthetic generation of ansamitocin derivatives
Oxalic acid formation from hydroxyl radical substitutions
Cyclization to produce CRF1 receptor antagonists
Preparation, optical and electrochemical studies of thiophene end capped olig(2,3-alkylthieno[3,4-b]pyrazine)
Asymmetrical synthesis of glycosyl chlorides and bromides

Uses

Leptin from rat has been used:

  • to check the effect of intranasal nerve growth factor (NGF) on NGF activity in the spinal cord of Sprague-Dawley rats
  • for validation of labelling for leptin-bearing cells of Sprague-Dawley rats
  • to study the effect of leptin on STAT3 (signal transducer and activator of transcription 3) phosphorylation in neural population of Sprague-Dawley rats
  • to study leptin response towards chemoreflex in nucleus of the solitary tract
  • in rats, to check the effect of association between leptin and neuronal nitric oxide pathway on penicillin-induced epileptiform activity

reaction suitability

reagent type: oxidant

Biochem/physiol Actions

Leptin is a hormone produced primarily in adipocytes, although leptin mRNA has also been identified in placenta and fetal tissues, gastric tissue and liver. Its primary site of action appears to be on neurons in the hypothalamus that are involved in regulating energy balance, appetite, and body weight. Leptin increases the production of nitric oxide in endothelial cells and stimulates angiogenesis in vitro and in vivo.Human and mouse leptin share ~84% sequence identity.

OXALYL BROMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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OXALYL BROMIDE Suppliers

Luofu Pharmaceutical Technology (Jiaxing) Co., Ltd
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View Lastest Price from OXALYL BROMIDE manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
OXALYL BROMIDE 15219-34-8
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-31
Hebei Yanxi Chemical Co., Ltd.
Product
OXALYL BROMIDE 15219-34-8
Price
US $20.00-1.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10 tons
Release date
2023-10-26

15219-34-8, OXALYL BROMIDERelated Search:


  • oxalyl bromide solution
  • OXALYL BROMO
  • BrCOCOBr
  • Ethanedioyl bromide
  • ethanedioyldibromide
  • Ethanedioyl-dibromide-
  • OXALYL BROMIDE, 2.0M SOLUTION IN DICHLOR OMETHANE
  • Dibromoethanedione
  • Oxalic acid dibromide
  • Oxalyl dibromide
  • Oxalyl bromide,98%
  • Oxalyl broMide, 98% 25GR
  • Oxalyl broMide 97%
  • NSC 96957
  • Ethanedioyl dibromide solution
  • Leptin from rat
  • Anti-CDH11 antibody produced in goat
  • CAD11
  • cadherin 11, type 2, OB-cadherin (osteoblast)
  • CDHOB
  • OB
  • OXALYL BROMIDE
  • Oxaly bromide
  • Oxayl Bromide
  • BRIGHTENER OB
  • Obesity Homolog
  • LEPD
  • Obese protein
  • 15219-34-8
  • C2Br2O2
  • Synthetic Reagents
  • Others
  • Oxidation
  • Others
  • Oxidation
  • Synthetic Reagents