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Merck

22790

2-Chloroacetamide

≥98.0% (HPLC)

Sinónimos:

Chloracetamide, alpha-Chloroacetamide

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250 G

MXP 1,029.00

MXP 1,029.00


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Fórmula lineal:
ClCH2CONH2
Número CAS:
Peso molecular:
93.51
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-174-2
Beilstein/REAXYS Number:
878191
MDL number:

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Nombre del producto

2-Chloroacetamide, ≥98.0% (HPLC)

InChI key

VXIVSQZSERGHQP-UHFFFAOYSA-N

InChI

1S/C2H4ClNO/c3-1-2(4)5/h1H2,(H2,4,5)

SMILES string

NC(=O)CCl

vapor pressure

0.05 mmHg ( 20 °C)

assay

≥98.0% (HPLC)

form

solid

mp

116-118 °C (lit.)
118-120 °C

solubility

methanol: soluble 1 g/10 mL
absolute ethanol: 10 part(lit.)
water: soluble 10 parts(lit.)
diethyl ether: very slightly soluble(lit.)

Quality Level

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1 of 4

Este artículo
C02672159013761
assay

≥98.0% (HPLC)

assay

≥98%

assay

≥98.0% (GC)

assay

≥98.0% (GC)

Quality Level

200

Quality Level

300

Quality Level

100

Quality Level

100

solubility

methanol: soluble 1 g/10 mL, water: soluble 10 parts(lit.), absolute ethanol: 10 part(lit.), diethyl ether: very slightly soluble(lit.)

solubility

-

solubility

chloroform: soluble(lit.), diethyl ether: soluble(lit.)

solubility

methanol: soluble 1 g/10 mL, clear, almost colorless

form

solid

form

powder

form

liquid

form

solid

mp

116-118 °C (lit.), 118-120 °C

mp

116-118 °C (lit.)

mp

-

mp

49-51 °C (lit.)

vapor pressure

0.05 mmHg ( 20 °C)

vapor pressure

0.05 mmHg ( 20 °C)

vapor pressure

-

vapor pressure

-

Application

2-Chloroacetamide was used in the synthesis of the derivatives of 1,8-naphthyridine containing thiono groups[1]. It was also used as a reagent for the synthesis of carboxamidomethyl esters as carboxyl protecting groups in peptide synthesis[2]

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Repr. 2 - Skin Sens. 1

Clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

338.0 °F

flash_point_c

170 °C

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Jun Zhang et al.
Journal of agricultural and food chemistry, 59(9), 4614-4621 (2011-03-23)
A butachlor-degrading strain, designated FLY-8, was isolated from rice field soil and was identified as Paracoccus sp. Strain FLY-8 could degrade and utilize six chloroacetamide herbicides as carbon sources for growth, and the degradation rates followed the order alachlor >
J. Martinez et al.
Tetrahedron Letters, 24, 5219-5219 (1983)
K Eszter Borbas et al.
Bioconjugate chemistry, 18(4), 1205-1212 (2007-06-23)
Targeted radiopharmaceuticals offer the possibility of improved tumor imaging and radiotherapy, with reduced side effects. A variety of monoclonal antibodies and antibody fragments have previously been successfully radiolabeled and used in diagnostic imaging and targeted radiotherapy of cancer. Many such
Cleonice Rocha et al.
Environmental pollution (Barking, Essex : 1987), 152(1), 239-244 (2007-07-17)
Solid-phase microextraction coupled with gas chromatography-mass spectrometry (SPME-GC-MS) was used to analyze two triazine (atrazine and simazine) and three chloroacetamide herbicides (acetochlor, alachlor, and metolachlor) in water samples from a midwest US agricultural drainage ditch for two growing seasons. The
Yasmine Souissi et al.
Journal of chromatography. A, 1310, 98-112 (2013-09-10)
The photooxidation of acetochlor (a pesticide belonging to the acetamides group) using a polychromatic UV irradiation in ultrapure water was studied. This study reports the efficiency of mass spectrometry for the characterization of photodegradation products of acetochlor. Decompositions of protonated

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