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2-Bromoethylamine hydrobromide

CAS No.
2576-47-8
Chemical Name:
2-Bromoethylamine hydrobromide
Synonyms
2BEHR;JACS-2576-47-8;BromoethylamineHbr;2-Bromoethanamine HBr;AMINOETHYL BROMIDE HBR;2-BROMOETHYLAMINE HBR 99%;2-(DIALLYLAMINO)ETHYLAMINE;2-Bromoethylazanium bromide;bromoethylamine,hydrobromide;2-BROMOETHYLAMMONIUM BROMIDE
CBNumber:
CB7232631
Molecular Formula:
C2H7Br2N
Molecular Weight:
204.89
MDL Number:
MFCD00012886
MOL File:
2576-47-8.mol
MSDS File:
SDS
Last updated:2026-01-13 11:25:19
Product description Number Pack Size Price
2-Bromoethylammonium bromide for synthesis 8.20176 100g $86.9
2-Bromoethylammonium bromide for synthesis 8.20176 500g $226
2-Bromoethylammonium bromide for synthesis 8.20176 5kg $679
2-Bromoethylammonium bromide for synthesis 8.20176 50kg $6280
2-Bromoethylamine hydrobromide purum, ≥97.0% (AT) 06670 100g $50.8
More product size

2-Bromoethylamine hydrobromide Properties

Melting point 172 °C
Boiling point 181.3℃[at 101 325 Pa]
Density 1.9061 (rough estimate)
vapor pressure 0.001Pa at 25℃
refractive index 1.5393 (estimate)
storage temp. Store below +30°C.
solubility >500g/l
form Crystalline Powder or Crystals
color White to light beige
PH 2.9 (10g/l, H2O, 20℃)
Water Solubility > 500 g/L (20 ºC)
Sensitive Hygroscopic
BRN 3607605
InChI 1S/C2H6BrN.BrH/c3-1-2-4;/h1-2,4H2;1H
InChIKey WJAXXWSZNSFVNG-UHFFFAOYSA-N
SMILES Br.NCCBr
LogP 0.795 at 25℃
CAS DataBase Reference 2576-47-8(CAS DataBase Reference)
EPA Substance Registry System 2-Bromoethylamine hydrobromide (2576-47-8)
UNSPSC Code 12352107
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H412
Precautionary statements  P264-P270-P273-P301+P312-P501
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi,C,Xn
Risk Statements  36/37/38-68-52/53-43-22
Safety Statements  26-36/37-61-36/37/39-36
WGK Germany  3
RTECS  KQ8225000
3-10
Hazard Note  Irritant
TSCA  TSCA listed
HazardClass  IRRITANT, CORROSIVE
HS Code  29211980
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Aquatic Chronic 3
Toxicity LD50 orally in Rabbit: > 200 - 2000 mg/kg
NFPA 704
0
2 1

2-Bromoethylamine hydrobromide price More Price(53)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.20176 2-Bromoethylammonium bromide for synthesis 2576-47-8 100g $86.9 2026-03-19 Buy
Sigma-Aldrich 8.20176 2-Bromoethylammonium bromide for synthesis 2576-47-8 500g $226 2026-03-19 Buy
Sigma-Aldrich 8.20176 2-Bromoethylammonium bromide for synthesis 2576-47-8 5kg $679 2026-03-19 Buy
Sigma-Aldrich 8.20176 2-Bromoethylammonium bromide for synthesis 2576-47-8 50kg $6280 2026-03-19 Buy
Sigma-Aldrich 06670 2-Bromoethylamine hydrobromide purum, ≥97.0% (AT) 2576-47-8 100g $50.8 2026-03-19 Buy
Product number Packaging Price Buy
8.20176 100g $86.9 Buy
8.20176 500g $226 Buy
8.20176 5kg $679 Buy
8.20176 50kg $6280 Buy
06670 100g $50.8 Buy

2-Bromoethylamine hydrobromide Chemical Properties,Uses,Production

Chemical Properties

slight yellow to white crystalline powder. Soluble in water and methanol, insoluble in ether. Hygroscopic and moisture sensitive. Incompatible with strong oxidizing agents.

Uses

2-Bromoethylamine hydrobromide is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone. It acts as a building block which is used for proteomics research. It is also used as organic and pharmaceutical intermediates for the preparation of first-aid medicines.

Application

2-Bromoethylamine hydrobromide (BEA-HBr) can be used as a reactant in the preparation of:
Amino-functionalized ionic liquid, 1-aminoethyl-3-methylimidazolium hexafluorophosphate ([2-aemim][PF6]). [2-aemim][PF6] is employed as a catalyst in the synthesis of 4H-pyrans derivatives by treating with aromatic aldehydes, malononitrile, ethyl acetoacetate via Knoevenagel condensation reaction.
2-(N-aryl-N-aroyl)amino-4,5-dihydrothiazole derivatives via cyclocondensation reaction.
It can be also employed as an alkylating agent for the surface modification of nylon to obtain primary/secondary/tertiary amine groups.

Preparation

2-Bromoethylamine hydrobromide was synthesized by bromination of ethanolamine. Drop into hydrobromic acid in the reaction pot, cool, add ethanolamine dropwise under stirring, and finish adding dropwise within half an hour, then steam the hydrobromic acid of 85% of the input quantity (the feed quantity of hydrobromic acid is 8.89 times the weight of ethanolamine) , about 20h steamed. After the concentrated solution is cooled to 70-80°C, it is put into pre-chilled acetone, cooled to below 5°C, and the crystallized 2-bromoethylamine hydrobromide is filtered out. Yield 70%.

General Description

Crystals.

Air & Water Reactions

Water soluble.

Reactivity Profile

The acidic organic salt (HBr) of the amine. Acidic salts are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition 2-Bromoethylamine hydrobromide emits very toxic fumes of bromide ion, NOx and hydrogen bromide.

Fire Hazard

Flash point data for 2-Bromoethylamine hydrobromide are not available; however, 2-Bromoethylamine hydrobromide is probably combustible.

141-43-5
2576-47-8
Synthesis of 2-Bromoethylamine hydrobromide from Monoethanolamine
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View Lastest Price from 2-Bromoethylamine hydrobromide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Bromoethylamine hydrobromide pictures 2026-04-23 2-Bromoethylamine hydrobromide
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US $5.00 / KG 1KG 99% 200mt/year Jinan Finer Chemical Co., Ltd
2-Bromoethylamine hydrobromide pictures 2025-12-01 2-Bromoethylamine hydrobromide
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US $0.00 / kg 1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
2-Bromoethylamine hydrobromide  pictures 2025-11-18 2-Bromoethylamine hydrobromide
2576-47-8
US $1.10 / g 1g 99.00% 100 Tons Min Dideu Industries Group Limited
2-bromoethanaminehydrobromide 2-bromo-ethanaminhydrobromide 2-bromo-ethylaminhydrobromide beta-bromoethylaminehydrobromide bromoethylamine,hydrobromide 2-bromo-2-ethylamine hydrobromide 2-Bromoethylazanium bromide 2-Bromoethylamine·hydrogen bromide 1-Amino-2-bromoethane hydrobromide 2-BroMoethylaMine hydrobroMide, 99% 100GR 2-BroMoethylaMine hydrobroMide, 99% 25GR 2-broMideethylaMinehydrobroMide EthanaMine,2-broMo-, hydrobroMide (1:1) 2-BroMoethylaMine hydrobroMide puruM, >=97.0% (AT) 2-BroMoethylaMine hydrobroMide, 98+%, 98+% 2- broMineethylaMinehydrobroMide 2-Aminoethyl bromide hydrobromide 2-bromoethanamine hydrobromide 2-Bromoethylamine hydrochloride 2-Bromoethylammonium bromide for synthesis Ethanamine,2-bromo-, hydrobromide (9CI) 2-(DIALLYLAMINO)ETHYLAMINE 2-BROMOETHYLAMINE HYDROBROMIDE 2-BROMOETHYLAMMONIUM BROMIDE 2-AMINOETHYL BROMIDE HYDROBROMIDE AMINOETHYL BROMIDE HBR AMINOETHYL BROMIDE HYDROBROMIDE 2-Bromoethylamine Hdrobromide 2-BROMOETHYLAMINE HYDROBROMIDECRYSTALLIN E 2-BromoethylamineHydrobromide99% BromoethylamineHbr 2-BromoethylamineHydrobromideForSynthesis 2-Bromoethylamine Hydrobromide 99% 2-bromoethylaminehydrobromate 1-Bromo-2-ethylamine hydrobromide 2-Bromoethylamine hydrobromide, 98+% Ethanamine, 2-bromo-, hydrobromide 2-BROMOETHYLAMINE HBR 99% 2-Bromoethylamine monohydrobromide JACS-2576-47-8 2-Bromoethylamine Hydrobromide > 2-Bromoethylamine hydrobromide, 99%, for synthesis 2-BROMOETHYLAMMONIUM BROMIDE FOR SYNTHES 2-Bromoethylamine hydrobromide ISO 9001:2015 REACH 2-Bromoethylamine HBR/2-Bromoethylamine hydrobromide 2-Bromoethylamine Hydrobromide extrapure AR, 99% 2-Bromoethanamine HBr BROMO ETHANOLAMINE HYDROBROMIDE 2-Bromo ethylene amine hydrobromide / 2-BEA 2BEHR 2-bromoethylaminehydrobromoacidsalt 2576-47-8 2567-47-8 C2H6BrNxHBr BrCH2CH2NH2HBr BrCH2CH2NH3Br C2H7Br2N C2H6BrNBrH C2H6BrN C2H6BrNHBr