23035
2-Chloroethylamine hydrochloride
purum, ≥98.0% (AT)
Sinônimo(s):
2-Aminoethyl chloride hydrochloride
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About This Item
Fórmula linear:
ClCH2CH2NH2 · HCl
Número CAS:
Peso molecular:
115.99
Beilstein:
3590304
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
grau
purum
Nível de qualidade
Ensaio
≥98.0% (AT)
forma
solid
pf
140-150 °C (lit.)
140-150 °C
cadeia de caracteres SMILES
Cl.NCCCl
InChI
1S/C2H6ClN.ClH/c3-1-2-4;/h1-2,4H2;1H
chave InChI
ONRREFWJTRBDRA-UHFFFAOYSA-N
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Categorias relacionadas
Aplicação
2-Chloroethylamine hydrochloride can be used in the preparation of novel Schiff base ligands. These ligands, when immobilized on silica gels, form inexpensive materials for the removal of metal ions such as Ni2+ and Co2+ ions from contaminated water.
Other applications:
Other applications:
- Alginate derivatization via aminoethylation to form aminoethyl alginate.
- Synthesis of N-(2-chloroethyl)-benzaldimine.
- Derivatization of starch to form aminoethyl (AE-St) starch derivatives.
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Dam. 1 - Met. Corr. 1 - Muta. 2 - Skin Corr. 1B
Código de classe de armazenamento
8A - Combustible corrosive hazardous materials
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Preparation of polypropylene based hyperbranched absorbent fibers and the study of their adsorption of CO2
Xu T, et al.
Royal Society of Chemistry Advances, 5(42), 32902-32908 (2015)
Production of L (+) lactic acid by Lactobacillus delbrueckii immobilized in functionalized alginate matrices.
Rao C S, et al.
World Journal of Microbiology & Biotechnology, 24(8), 1411-1415 (2008)
Chemical modification of silica gel with synthesized new Schiff base derivatives and sorption studies of cobalt (II) and nickel (II).
Kursunlu A N, et al.
Applied Surface Science, 255(21), 8798-8803 (2009)
Khalil Sakeer et al.
Carbohydrate polymers, 163, 108-117 (2017-03-08)
Different starch derivatives were evaluated as supports for attachment and recovery of macrophages (RAW 264.7 line). Gelatinized starch (G-St), acetate starch (Ac-St), carboxymethyl starch and aminoethyl starch were synthesized and characterized by FTIR, 1H NMR, SEM and static water contact
Joachim F R Van Guyse et al.
Polymers, 13(3) (2021-02-04)
Smart or adaptive materials often utilize stimuli-responsive polymers, which undergo a phase transition in response to a given stimulus. So far, various stimuli have been used to enable the modulation of drug release profiles, cell-interactive behavior, and optical and mechanical
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