T85308
Tris(2-chloroethyl)amine hydrochloride
98%
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About This Item
Fórmula linear:
(ClCH2CH2)3N·HCl
Número CAS:
Peso molecular:
240.99
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
Preço e disponibilidade não estão disponíveis no momento.
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Nível de qualidade
Ensaio
98%
pf
127-130 °C (lit.)
cadeia de caracteres SMILES
Cl.ClCCN(CCCl)CCCl
InChI
1S/C6H12Cl3N.ClH/c7-1-4-10(5-2-8)6-3-9;/h1-6H2;1H
chave InChI
VEAUDLLZYJVHRI-UHFFFAOYSA-N
Categorias relacionadas
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 2 Oral - Carc. 2 - Skin Corr. 1B
Código de classe de armazenamento
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic 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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Trichloromethyl ketones as synthetically versatile donors: application in direct catalytic mannich-type reactions and the stereoselective synthesis of azetidines.
Hiroyuki Morimoto et al.
Angewandte Chemie (International ed. in English), 45(19), 3146-3150 (2006-04-06)
N I Riabchenko et al.
Radiobiologiia, 31(1), 22-26 (1991-01-01)
Regularities of chromatin degradation in thymocytes and LS/BL tumor cells have been investigated. It has been shown that the rate of DNA degradation by Ca/Mg-dependent endonuclease in LS/BL tumor cells is 25 times lower than that in thymocytes, and radiation
D B Wildenauer et al.
Biochimica et biophysica acta, 603(1), 101-116 (1980-12-02)
The influence of tris(2-chloroethyl)amine on shape changes of human erythrocytes and ghosts was studied in vitro and correlated with alterations in the molecular structure of the membrane. (1) Reaction with 1--2 mM tris(2-chloroethyl)amine, a concentration which caused polymerisation of spectrin
L Szinicz et al.
Arzneimittel-Forschung, 31(10), 1713-1717 (1981-01-01)
The effect of tris-(2-chloroethyl)-amine (HN-3) on RNA and DNA was investigated spectrophotometrically. The shift in the absorbance spectrum caused by the addition of HN-3 was used to test a variety of compounds for their ability to inhibit RNA alkylation. The
T Hiratsuka
Biochemistry, 27(11), 4110-4114 (1988-05-31)
The chemotherapeutic alkylating reagent tris(2-chloroethyl)amine (TCEA) was used as a trifunctional cross-linking reagent with a cross-linking span of 5 A for myosin subfragment 1 (S-1). When S-1 was incubated with TCEA, all three domains of 20, 26, and 50 kDa
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