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B38503

Sigma-Aldrich

Bis(2-chloroethyl)amine hydrochloride

98%

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Linear Formula:
(ClCH2CH2)2NH·HCl
CAS Number:
821-48-7
Molecular Weight:
178.49
Beilstein:
3550356
EC Number:
212-479-5
MDL number:
MFCD00012515
PubChem Substance ID:
24891737
NACRES:
NA.22

Assay

98%

form

powder

mp

212-214 °C (lit.)

SMILES string

Cl.ClCCNCCCl

InChI

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

InChI key

YMDZDFSUDFLGMX-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
C42602T85308100870
Bis(2-chloroethyl)amine hydrochloride 98%

Sigma-Aldrich

B38503

Bis(2-chloroethyl)amine hydrochloride

1-(2-Chloroethyl)piperidine hydrochloride 98%

Sigma-Aldrich

C42602

1-(2-Chloroethyl)piperidine hydrochloride

Tris(2-chloroethyl)amine hydrochloride 98%

Sigma-Aldrich

T85308

Tris(2-chloroethyl)amine hydrochloride

Bis(4-chlorophenyl)acetic acid 98%

Sigma-Aldrich

100870

Bis(4-chlorophenyl)acetic acid

form

powder

form

crystals

form

-

form

-

mp

212-214 °C (lit.)

mp

230-232 °C (lit.)

mp

127-130 °C (lit.)

mp

167-169 °C (lit.)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

-

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H290 - H302 - H314

Hazard Classifications

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

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

No information available.

Flash Point(C)

No information available.

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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
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
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
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