3-Bromopropylamine hydrobromide, 98%, Thermo Scientific Chemicals
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3-Bromopropylamine hydrobromide, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Bromopropylamine hydrobromide, 98%, Thermo Scientific Chemicals

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100 g
25 g
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Catalog number B23254.22
also known as B23254-22
Price (EUR)/ Each
119,70
Online exclusive
133.00 
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Quantity:
100 g
Request bulk or custom format
Price (EUR)/ Each
119,70
Online exclusive
133.00 
Save 13,30 (10%)
Add to cart
3-Bromopropylamine hydrobromide, 98%, Thermo Scientific Chemicals
Catalog numberB23254.22
Price (EUR)/ Each
119,70
Online exclusive
133.00 
Save 13,30 (10%)
-
Add to cart
Chemical Identifiers
CAS5003-71-4
IUPAC Namehydrogen 3-bromopropan-1-amine bromide
Molecular FormulaC3H9Br2N
InChI KeyPQIYSSSTRHVOBW-UHFFFAOYSA-N
SMILES[H+].[Br-].NCCCBr
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream to pale pink
FormPowder
Assay (Titration ex Bromide)≥97.5 to ≤102.5%
Identification (FTIR)Conforms
Water Content (Karl Fischer Titration)≤1.0%
3-Bromopropylamine hydrobromide is used as pharmaceutical raw materials and intermediates. Homotaurine is synthesized from 3-bromopropylamine hydrobromide.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

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

Solubility
Soluble in water (50 mg/ml).

Notes
Hygroscopic. Store under inert gas. Store away from oxidizing agents, moisture.
RUO – Research Use Only

General References:

  1. Eleanor D. Bates; Rebecca D. Mayton; Ioanna Ntai and James H. Davis , Jr. CO2 Capture by a Task-Specific Ionic Liquid. J. Am. Chem. Soc. 2002, 124 (6), 926-927.
  2. R. F. Parcell; F. P. HauckJr. The Preparation of Tetrahydropyridines from Enamines and Imines. J. Org. Chem. 1963, 28 (12), 3468-3473.