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5003-71-4 Usage


3-Bromopropylamine hydrobromide is an organic compound that exists as a white to off-white powder or chunks. It is a valuable chemical intermediate and raw material in the pharmaceutical industry, known for its versatility in synthesizing various compounds.


Used in Pharmaceutical Industry:
3-Bromopropylamine hydrobromide is used as a pharmaceutical raw material and intermediate for the synthesis of Homotaurine, a compound with potential applications in the medical field.
Used in Chemical Synthesis:
3-Bromopropylamine hydrobromide is commonly used as a reagent to introduce a propylamine group to the molecular skeleton, which is essential in the creation of various chemical compounds.
Used in Synthesis of Azobenzene Rotaxane and Indolocarbazole-Containing [2]Rotaxane:
3-Bromopropylamine hydrobromide is utilized in the synthesis of photochemically and thermally reactive azobenzene rotaxane and indolocarbazole-containing [2]rotaxane, which are complex molecular structures with potential applications in molecular machines and materials science.
Used in Synthesis of Anticancer Agents:
In the field of oncology, 3-Bromopropylamine hydrobromide is employed in the synthesis of indenoisoquinoline-based active topoisomerase I inhibitors. These compounds have shown potential as anticancer agents, targeting the enzyme topoisomerase I, which plays a crucial role in DNA replication and is often overexpressed in cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 5003-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5003-71:
54 % 10 = 4
So 5003-71-4 is a valid CAS Registry Number.

5003-71-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B23254)  3-Bromopropylamine hydrobromide, 98%   

  • 5003-71-4

  • 25g

  • 371.0CNY

  • Detail
  • Alfa Aesar

  • (B23254)  3-Bromopropylamine hydrobromide, 98%   

  • 5003-71-4

  • 100g

  • 1241.0CNY

  • Detail
  • Aldrich

  • (B79803)  3-Bromopropylaminehydrobromide  98%

  • 5003-71-4

  • B79803-25G

  • 369.72CNY

  • Detail
  • Aldrich

  • (B79803)  3-Bromopropylaminehydrobromide  98%

  • 5003-71-4

  • B79803-100G

  • 1,240.20CNY

  • Detail



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017


1.1 GHS Product identifier

Product name 3-Bromopropylamine hydrobromide

1.2 Other means of identification

Product number -
Other names 1-Propanamine, 3-bromo-, hydrobromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5003-71-4 SDS

5003-71-4Upstream product

5003-71-4Relevant articles and documents

α-Substitution effects on the ease of S → N-Acyl transfer in aminothioesters

El-Gendy, Bahaa El-Dien M.,Ghazvini Zadeh, Ebrahim H.,Sotuyo, Ania C.,Pillai, Girinath G.,Katritzky, Alan R.

, p. 577 - 582 (2013/07/11)

In S-acylcysteines and homocysteines, the efficacy and rate of S → N-acyl transfer (5 and 6 cyclic TSs) vary with the size of S-acyl group. Conformational and quantum chemical calculations indicate that the spatial distance, b(N-C), between the terminal amine and the thioester carbon is shortened by α-C(O)X (X=OH, OMe, NH2) substituents. Spatial distance, b(N-C), between the terminal amine and the thioester carbon is shortened by α-C(O)X (X=OH, OMe, NH2) substituents.

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