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Merck
CN

B38503

双(2-氯乙基)胺 盐酸盐

98%

别名:

β,β′-二氯乙基胺盐酸盐, 1,5-二氯-3-氮杂戊烷盐酸盐, 2,2′-Di氯乙基胺盐酸盐, 2-氯-N-(2-氯乙基)乙胺盐酸盐, N,N-双(2-氯乙基)胺盐酸盐, 二(2-氯乙基)胺盐酸盐, 双(β-氯乙基)胺盐酸盐, 双(2-氯乙基)氯化铵, 双(2-氯乙基)胺盐酸盐, 盐酸氮芥Nornitrogen mustard hydrochloride

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关于此项目

线性分子式:
(ClCH2CH2)2NH·HCl
化学文摘社编号:
分子量:
178.49
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-479-5
Beilstein/REAXYS Number:
3550356
MDL number:
Assay:
98%
Form:
powder
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InChI key

YMDZDFSUDFLGMX-UHFFFAOYSA-N

InChI

1S/C4H9Cl2N.ClH/c5-1-3-7-4-2-6;/h7H,1-4H2;1H

SMILES string

Cl.ClCCNCCCl

assay

98%

form

powder

mp

212-214 °C (lit.)

Quality Level

General description

双(2-氯乙基)胺盐酸盐可作为起始材料合成哌嗪衍生物。

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

No information available.

flash_point_c

No information available.

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Joanna Cytarska et al.
Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 27(3), 303-311 (2019-04-13)
Synthesis, characterization and investigation of antiproliferative activity of nine triazene salts against human cancer cells lines (MV-4-11, MCF-7, JURKAT, HT-29, Hep-G2, HeLa, Du-145 and DAUDI), and normal human mammary epithelial cell line (MCF7-10A) is presented. The structures of novel compounds
S Papot et al.
Bioorganic & medicinal chemistry letters, 10(16), 1835-1837 (2000-09-02)
A new glucuronylated prodrug of nornitrogen mustard, incorporating the same spacer group as the doxorubicin prodrug HMR 1826, has been prepared. Upon exposure to E. coli beta-glucuronidase, fast hydrolysis occurs but a lower cytotoxicity against LoVo cancer cells is observed
K Hemminki
Chemico-biological interactions, 61(1), 75-88 (1987-01-01)
Nornitrogen mustard was shown to bind to the N-7 position of guanine in DNA and guanosine. The initial binding product was NOR-G. N-(2-chloroethyl)-N-[2-(7-guaninyl)ethyl]amine but it was converted with time to a hydroxylated derivative. NOR-OH-G and to a cross-link, G-NOR-G. The
K Hemminki et al.
Archives of toxicology, 61(2), 126-130 (1987-12-01)
A gas chromatographic (GC-ECD) method was developed for the determination of nornitrogen mustard (NOR) and its hydrolysis products. The method was based on derivatization by heptafluorobutyric anhydride. The structures of the derivatives of NOR were established by GC-MS. The method
H Lu et al.
Journal of chromatography. B, Biomedical applications, 678(2), 219-225 (1996-04-12)
A sensitive and specific method for the quantitative analysis of N-2-chloroethylaziridine (CEA), a volatile cytotoxic metabolite of cyclophosphamide, has been developed using gas chromatography-mass spectrometry and stable isotope dilution techniques. The high volatility problem of CEA during isolation procedure was

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