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Thermo Scientific Chemicals Chloroform, Molecular Biology Reagent

$149.88 - $494.73

Chemical Identifiers

CAS 67-66-3
Molecular Formula CHCl3
Molecular Weight (g/mol) 119.37
MDL Number MFCD00000826
InChI Key HEDRZPFGACZZDS-UHFFFAOYSA-N
Synonym trichloromethane, formyl trichloride, methane, trichloro, trichloroform, methane trichloride, methenyl trichloride, methyl trichloride, trichlormethan, chloroforme, cloroformio
PubChem CID 6212
ChEBI CHEBI:35255
SMILES ClC(Cl)Cl
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Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAJ67241AP
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Thermo Scientific Chemicals
J67241AP
500 mL
Each for $149.88
 
AAJ67241K2
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Thermo Scientific Chemicals
J67241K2
1 L
Each for $246.55
 
AAJ67241K4
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Thermo Scientific Chemicals
J67241K4
2.5 L
Each for $494.73
 
Description

Description

Chloroform is a common laboratory reagent favored for use as a solvent due to the compounds relative unreactivity and miscibility with most organic compounds. Chloroform is also used in organic synthesis as a source for CCl2. In the swine tracheal smooth muscle, chloroform has been demonstrated to directly and in a concentration dependent manner induce contractions. It has been observed that Chloroform can release Ca2+ from ryanodine sensitive receptors in chloroform-induced contraction in swine tracheal smooth muscle. At concentrations of 100 and 250 ppm in mouse splenocyte, basal proliferation was increased yet a decrease in circulating neutrophils was documented.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Chloroform is a common laboratory reagent favored for use as a solvent due to the compounds relative unreactivity and miscibility with most organic compounds. Chloroform is also used in organic synthesis as a source for CCl2. In the swine tracheal smooth muscle, chloroform has been demonstrated to directly and in a concentration dependent manner induce contractions. It has been observed that Chloroform can release Ca2+ from ryanodine sensitive receptors in chloroform-induced contraction in swine tracheal smooth muscle. At concentrations of 100 and 250 ppm in mouse splenocyte, basal proliferation was increased yet a decrease in circulating neutrophils was documented.

Solubility
Soluble in water at 20°C 8 g/L.

Notes
Stabilized with approx. 50 ppm amylene
Specifications

Chemical Identifiers

67-66-3
119.37
HEDRZPFGACZZDS-UHFFFAOYSA-N
6212
ClC(Cl)Cl
CHCl3
MFCD00000826
trichloromethane, formyl trichloride, methane, trichloro, trichloroform, methane trichloride, methenyl trichloride, methyl trichloride, trichlormethan, chloroforme, cloroformio
CHEBI:35255

Specifications

-63°C
Colorless
61°C
Characteristic
1.446
MFCD00000826
1731042
trichloromethane, formyl trichloride, methane, trichloro, trichloroform, methane trichloride, methenyl trichloride, methyl trichloride, trichlormethan, chloroforme, cloroformio
HEDRZPFGACZZDS-UHFFFAOYSA-N
chloroform
6212
119.38
67-66-3
1.492 g/mL
500 mL
Liquid
CHCl3
UN1888
14,2141
Soluble in water at 20°C 8g/L.
ClC(Cl)Cl
119.37
CHEBI:35255
Chloroform, Molecular Biology Reagent
Safety and Handling

Safety and Handling

GHS H Statement
H351-H373-H302-H315
Suspected of causing cancer.
May cause damage to organs through prolonged or repeated exposure.
Harmful if swallowed.
Causes skin irritation.

P201-P202-P260-P264b-P270-P271-P280i-P281-P301+P312-P302+P352-P304+P340-P305+P351+P338-P308+P313-P330-P332+P313-P362-P501c

H302-H315-H319-H331-H335-H336-H351-H361d-H373

DOTInformation : Transport Hazard Class: 6.1; Packaging Group: III; Proper Shipping Name: CHLOROFORM

EINECSNumber : 200-663-8

RTECSNumber : FS9100000

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only