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Merck
CN

10907

Chloroacetaldehyde solution

Wacker Chemie AG, ≥45.0% in H2O (density determination)

Synonym(s):

CLACH

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About This Item

Linear Formula:
ClCH2CHO
CAS Number:
Molecular Weight:
78.50
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-472-8
Beilstein/REAXYS Number:
1071226
MDL number:
Form:
solid
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form

solid

Quality Level

manufacturer/tradename

Wacker Chemie AG

concentration

≥45.0% in H2O (density determination)

bp

80-100 °C (lit.)

functional group

aldehyde, chloro

SMILES string

[H]C(=O)CCl

InChI

1S/C2H3ClO/c3-1-2-4/h2H,1H2

InChI key

QSKPIOLLBIHNAC-UHFFFAOYSA-N

Application

Chloroacetaldehyde is a reagent used for converting adenine and its nucleoseides into fluorescent etheno derivatives which can be analysed by HPLC. It was used for derivatization in fluorometric determination of arprinocid and analogous compounds in human plasma .

Biochem/physiol Actions

Chloroacetaldehyde, a metabolite of ifosamide, influences oxidative phosphorylation in mitochondria. It causes breaking of DNA strands and strongly inhibits DNA synthesis.

Other Notes

prices for bulk quantities on request


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Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Preparation, titration, and storage of chloroacetaldehyde for fluorometric determination of adenine and its derivatives.
McCann WP, et al.
Analytical Chemistry, 55(8), 1454-1455 (1983)
Svenja K Brüggemann et al.
Cancer chemotherapy and pharmacology, 57(3), 349-356 (2005-09-01)
The ifosfamide metabolite chloroacetaldehyde had been made responsible for side effects only. We found in previous studies a strong cytotoxicity on human MX-1 tumor cells and xenografts in nude mice. Chloroacetaldehyde is supposed to act via alkylation or by inhibition
Fluorogenic reaction between adenine derivatives and chloroacetaldehyde and its application to the determination of 9-(2-chloro-6-fluorobenzyl) adenine in human plasma.
Matuszewski BK and Bayne WF.
Analytica Chimica Acta, 227, 189-202 (1989)



Global Trade Item Number

SKUGTIN
05-0670-5-500G-J04061832570174
378801-25G04061831836370
449717-25G04061838076151
NIST18004061834140153
102840100004022536037448
102840905004022536037462
449717-5G04061838103055
944335-50G04065273550665
10907-1KG04061838687838
10907-230KG04061836698508
10907-25KG04061836681890