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N-BROMOACETAMIDE

Product Name:
N-BROMOACETAMIDE
CAS No.
79-15-2
Chemical Name:
N-BROMOACETAMIDE
CBNumber:
CB6176246
Molecular Formula:
C2H4BrNO
Formula Weight:
137.96
MOL File:
79-15-2.mol
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N-BROMOACETAMIDE Property

Melting point:
102-105°C
Boiling point:
127-130 °C(Press: 16 Torr)
Density 
1.7000 (rough estimate)
refractive index 
1.4740 (estimate)
storage temp. 
−20°C
pka
9.41±0.46(Predicted)
form 
powder
color 
white to yellow
Water Solubility 
Soluble in water.
Merck 
14,1398
BRN 
969346
CAS DataBase Reference
79-15-2(CAS DataBase Reference)
EPA Substance Registry System
N-Bromoacetamide (79-15-2)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
3261
WGK Germany 
3
8
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29299090
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N-Bromosuccinimide Price More Price(5)

Sigma-Aldrich Gold
Product number:
B2377
Product name :
N-Bromoacetamide
Purity:
powder
Packaging:
50g
Price:
$392
Updated:
2019/12/02
Buy:
Buy
TCI Chemical Gold
Product number:
B0530
Product name :
N-Bromoacetamide
Purity:
>97.0%(T)
Packaging:
5g
Price:
$61
Updated:
2020/06/24
Buy:
Buy
TCI Chemical Gold
Product number:
B0530
Product name :
N-Bromoacetamide
Purity:
>97.0%(T)
Packaging:
25g
Price:
$173
Updated:
2020/06/24
Buy:
Buy
Alfa Aesar Gold
Product number:
L02953
Product name :
N-Bromoacetamide, 95%
Packaging:
25g
Price:
$280
Updated:
2020/06/24
Buy:
Buy
Alfa Aesar Gold
Product number:
L02953
Product name :
N-Bromoacetamide, 95%
Packaging:
5g
Price:
$77.7
Updated:
2020/06/24
Buy:
Buy
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N-BROMOACETAMIDE Chemical Properties,Usage,Production

General Description

White powder.

Air & Water Reactions

Soluble in water.

Reactivity Profile

N-BROMOACETAMIDE is sensitive to light, moisture, and heat. . N-BROMOACETAMIDE decomposes rapidly at elevated temperatures, in the presence of moisture and light.

Fire Hazard

Flash point data are not available for N-BROMOACETAMIDE, but N-BROMOACETAMIDE is probably combustible.

Purification Methods

A possible contaminant is CH3CONBr2. Recrystallise it from CHCl3/hexane (1:1, seed if necessary) or water and dry over CaCl2. It is a brominating agent. [Oliveto & Gerold Org Synth Coll Vol IV 104 1963.] Alternatively, dissolve it in the minimum volume of warm H2O (60o), then cool in an ice bath, collect the crystals and dry them in an anhydrous atmosphere, dissolve in Et2O, chill and evaporate till crystallisation. Dry the crystals in vacuo at 25o, then at 45o (m 108o). Crystallise from CHCl3 (m 103o). Estimate the available Br iodometrically [Buckles et al. J Org Chem 23 483 1958]. [Beilstein 2 H 181, 2 I 82, 2 II 180, 2 III 406, 2 IV 417.]

N-BROMOACETAMIDE Preparation Products And Raw materials Raw materials

Raw materials

Preparation Products

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N-BROMOACETAMIDE Suppliers

Global(93)Suppliers
J & K SCIENTIFIC LTD.
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400-610-6006; 021-67582000
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021-67582001/03/05
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Syntechem Co.,Ltd
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79-15-2, N-BROMOACETAMIDERelated Search:

N1-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]-2-bromoacetamide 2-Bromo-2'-(trifluoromethyl)acetanilide 2-Bromo-3'-(trifluoromethyl)acetanilide N-(3-ACETYLPHENYL)-2-BROMOACETAMIDE N1-(4-METHOXY-1,3-BENZOTHIAZOL-2-YL)-2-BROMOACETAMIDE tempo 4-bromoacetamide 2-BROMO-4-(TRIFLUOROMETHYL)ACETANILIDE N-(2-benzoylphenyl)-2-bromoacetamide,N1-(2-BENZOYLPHENYL)-2-BROMOACETAMIDE TEXAS RED(R) C5 BROMOACETAMIDE N1-(4-BROMOPHENYL)-2-BROMOACETAMIDE N1-{4-BROMO-3-[4-(TERT-BUTYL)PHENYL!-1H-PYRAZOL-5-YL}-2-BROMOACETAMIDE, TECH 3-Bromo-1-chloro-5,5-dimethylhydantoin N-BROMOCAPROLACTAM N-BROMOPHTHALIMIDE N-Bromosuccinimide 1,3-Dibromo-5,5-dimethylhydantoin N-BROMOSACCHARIN 1,3-DIBROMO-5-ETHYL-5-METHYLHYDANTOIN
  • 2-[2-(dimethylamino)ethoxymethoxy]-N,N-dimethylethanamine
  • N-BROMOACETAMIDE
  • NBAAcetobromamide
  • n-bromo-acetamid
  • ACETOBROMAMIDE
  • N-BROMOACETAMIDE (NBA)
  • AcetaMide, N-broMo-
  • <i>N</i>-Bromoacetamide
  • N-Bromacetamid
  • 79-15-2
  • CH3CONHBr
  • C2H4BORn
  • Bromination
  • Fusarinine -C Ornithinesterase
  • Enzymes, Inhibitors, and Substrates
  • D to K
  • Enzyme Inhibitors by Enzyme
  • Enzyme Inhibitors
  • Biochemicals and Reagents
  • BioChemical
  • Halogenation
  • Bromination
  • Halogenation
  • Synthetic Organic Chemistry