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4-Bromobenzylamine hydrochloride, 98%
4-Bromobenzylamine hydrochloride, 98%
4-Bromobenzylamine hydrochloride, 98%
Thermo Scientific Chemicals

4-Bromobenzylamine hydrochloride, 98%

CAS: 26177-44-6 | C7H9BrClN | 222.51 g/mol
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Catalog number A10979.18
also known as A10979-18
Price (USD)
635.65
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Ends: 30-Jun-2026
748.00
Save 112.35 (15%)
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Quantity:
50 g
Request bulk or custom format
Price (USD)
635.65
Special offer
Online exclusive
Ends: 30-Jun-2026
748.00
Save 112.35 (15%)
Each
Chemical Identifiers
CAS26177-44-6
IUPAC Namehydrogen 1-(4-bromophenyl)methanamine chloride
Molecular FormulaC7H9BrClN
InChI KeyBVYUYDBWQMSOKM-UHFFFAOYSA-N
SMILES[H+].[Cl-].NCC1=CC=C(Br)C=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
Water Content (Karl Fischer Titration)≤5.0%
Melting Point268-280°C
Appearance (Color)White to pale cream or pale yellow
FormPowder or crystalline powder or granules
4-Bromobenzylamine hydrochloride is used to study the characteristics of C-terminal polyamine modification in the presence of protease and amine. Further, it is used to prepare 1-(4-Brombenzyl)-pyrrole by reacting with 2,5-dimethoxy-tetrahydro-furan.

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
4-Bromobenzylamine hydrochloride is used to study the characteristics of C-terminal polyamine modification in the presence of protease and amine. Further, it is used to prepare 1-(4-Brombenzyl)-pyrrole by reacting with 2,5-dimethoxy-tetrahydro-furan.

Solubility
Soluble in water.

Notes
Hygroscopic. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Nortcliffe, A.; Moody, C. J. Seven-membered ring scaffolds for drug discovery: Access to functionalised azepanes and oxepanes through diazocarbonyl chemistry. Bioorg. Med. Chem. 2015, 23 (11), 2730-2735.
  2. Congiu, C.; Onnis, V.; Deplano, A.; Salvadori, S.; Marconi, V.; Maftei, D.; Negric, L.; Roberta Lattanzi, R.; Balboni, G. A new convenient synthetic method and preliminary pharmacological characterization of triazinediones as prokineticin receptor antagonists. Eur. J. Med. Chem. 2014, 81, 334-340.