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About This Item
Linear Formula:
BrCH2CH2NH2 · HBr
CAS Number:
Molecular Weight:
204.89
Beilstein:
3607605
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
grade
purum
Quality Level
Assay
≥97.0% (AT)
form
crystalline
bp
181.3 °C/979.2 hPa
mp
170-175 °C (lit.)
170-175 °C
solubility
water: soluble 84.02 g/L at 28 °C
soluble
density
0.98 g/cm3 at 28.3 °C
functional group
amine
bromo
SMILES string
Br.NCCBr
InChI
1S/C2H6BrN.BrH/c3-1-2-4;/h1-2,4H2;1H
InChI key
WJAXXWSZNSFVNG-UHFFFAOYSA-N
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Application
2-Bromoethylamine hydrobromide (BEA-HBr) can be used as a reactant in the preparation of:
It can be also employed as an alkylating agent for the surface modification of nylon to obtain primary/secondary/tertiary amine groups.
- 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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
142.9 °F - Pensky-Martens closed cup
Flash Point(C)
61.6 °C - Pensky-Martens closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and QSAR Studies in 2-(N-aryl-N-aroyl) amino-4, 5-dihydrothiazole Derivatives as Potential Antithrombotic Agents
Saxena AK, et al.
Bioorganic & Medicinal Chemistry, 9(8), 2025-2034 (2001)
Amino-functionalized ionic liquid as an efficient and recyclable catalyst for Knoevenagel reactions in water
Cai Y, et al.
Catalysis Letters, 109(1-2), 61-64 (2006)
Nylon surface modification. Part 1. Targeting the amide groups for selective introduction of reactive functionalities
Jia X, et al.
Polymer, 47(14), 4916-4924 (2006)
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