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3-Bromopropylamine hydrobromide

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3-Bromopropylamine hydrobromide Basic information

Product Name:
3-Bromopropylamine hydrobromide
Synonyms:
  • 1-amino-3-bromopropanehydrobromide
  • 3-bromo-1-propanaminhydrobromide
  • 3-bromopropanaminehydrobromide
  • 3-bromo-propylaminhydrobromide
  • 3-Bromopropylamine Hydrobromate
  • 1-Propanamine, 3-bromo-, hydrobromide
  • 3-BROMOPROPYLAMINE HYDROBROMIDE 98%
  • 3-bromopropan-1-amine hydrobromide
CAS:
5003-71-4
MF:
C3H9Br2N
MW:
218.92
EINECS:
225-675-0
Product Categories:
  • Amine Salts
  • Building Blocks
  • omega-Functional Alkanols, Carboxylic Acids, Amines & Halides
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • omega-Haloalkylamines
  • bc0001
  • 5003-71-4
Mol File:
5003-71-4.mol
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3-Bromopropylamine hydrobromide Chemical Properties

Melting point:
171-172 °C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
form 
Powder or Chunks
color 
White to off-white
Water Solubility 
Soluble in water (50 mg/ml).
Sensitive 
Hygroscopic
BRN 
3906418
InChI
InChI=1S/C3H8BrN.BrH/c4-2-1-3-5;/h1-3,5H2;1H
InChIKey
PQIYSSSTRHVOBW-UHFFFAOYSA-N
SMILES
C(CBr)CN.Br
CAS DataBase Reference
5003-71-4(CAS DataBase Reference)
EPA Substance Registry System
1-Propanamine, 3-bromo-, hydrobromide (5003-71-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
UH9925000
TSCA 
Yes
HS Code 
29211980

MSDS

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3-Bromopropylamine hydrobromide Usage And Synthesis

Chemical Properties

white to off-white powder or chunks

Uses

3-Bromopropylamine hydrobromide is used as pharmaceutical raw materials and intermediates. Homotaurine is synthesized from 3-bromopropylamine hydrobromide.

Uses

3-Bromopropylamine hydrobromide is commonly used as a reagent to introduce propylamine group to the molecular skeleton. Some of the other reported applications include:

  • Synthesis of photochemically and thermally reactive azobenzene rotaxane and indolocarbazole-containing [2]rotaxane.
  • Synthesis of indenoisoquinoline based active topoisomerase I inhibitors as anticancer agents.

Synthesis

Add the mixture of 3-amino-1-propanol (1ml, 13.3mmol) and 48% HBr (10ml, 40mmol) into the round-bottomed flask and reflux for 15h. Water and HBr were then distilled from the mixture under vacuum. The mixture was further dried under vacuum through a KOH/CaCl column to give 3-Bromopropylamine hydrobromide (2.95 g, 100%) as a brown solid.

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