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Merck

366919

Chloroforme

ACS spectrophotometric grade, ≥99.8%, contains 0.5-1.0% ethanol as stabilizer

Synonyme(s) :

Trichlorométhane, Trichlorure de méthylidyne

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About This Item

Formule empirique (notation de Hill) :
CHCl3
Numéro CAS:
67-66-3
Poids moléculaire :
119.38
UNSPSC Code:
12191502
NACRES:
NA.04
PubChem Substance ID:
329755456
MDL number:
MFCD00000826
Beilstein/REAXYS Number:
1731042
grade:
ACS spectrophotometric grade
assay:
≥99.8%
technique(s):
UV/Vis spectroscopy: suitable
bp:
60.5-61.5 °C (lit.)
vapor pressure:
160 mmHg ( 20 °C)

Nom du produit

Chloroforme, ACS spectrophotometric grade, ≥99.8%, contains 0.5-1.0% ethanol as stabilizer

InChI

1S/CHCl3/c2-1(3)4/h1H

SMILES string

ClC(Cl)Cl

InChI key

HEDRZPFGACZZDS-UHFFFAOYSA-N

grade

ACS spectrophotometric grade

vapor density

4.1 (vs air)

vapor pressure

160 mmHg ( 20 °C)

assay

≥99.8%

form

liquid

contains

0.5-1.0% ethanol as stabilizer

technique(s)

UV/Vis spectroscopy: suitable

impurities

Acetone and aldehyde, passes test
 Acid and chloride, passes test
 Free chlorine (Cl), passes test
 H2SO4, passes test (darkened)
<0.03% water

evapn. residue

<0.001%

color

APHA: ≤10

refractive index

n20/D 1.445 (lit.)

bp

60.5-61.5 °C (lit.)

mp

−63 °C (lit.)

density

1.48 g/mL at 25 °C (with ethanol stabilizer)
1.492 g/mL at 25 °C (lit.)

cation traces

Pb: ≤0.05 ppm

λ

H2O reference

UV absorption

λ: 245 nm Amax: 1.00
λ: 255 nm Amax: 0.25
λ: 260 nm Amax: 0.15
λ: 270 nm Amax: 0.05
λ: 290-400 nm Amax: 0.01

Quality Level

100

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Catégories apparentées

Application

Chloroform (spectrophotometric grade) was used in the following processes:
  • Synthesis of colloidal hydrophobic CdSe core nanocrystals (quantum dots).
  • Preparing phospholipid solutions.
  • As a solvent in the photolysis reaction of ruthenium complexes.
It may be used as:
  • Solvent for recrystallization.
  • Reference compound to detect the presence of chloroform in Tobacco smokes.
  • Extractant in solvent extraction process.

General description

Chloroform is a is a colorless, volatile chlorinated organic solvent whose vapors have narcotic effect. It is susceptible to degradation with time which can be suppressed by adding ethanol as a stabilizer. Since ethanol is added in higher concentration it leads to increase in polarity which may have a potential influence on some of the applications. Spectrophotometric grade chloroform shows low UV absorption which makes it an ideal solvent for spectrophotometry.

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Oral - STOT SE 3

target_organs

Central nervous system, Liver,Kidney

Classe de stockage

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk

WGK 3

flash_point_f

does not flash

flash_point_c

does not flash

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Certificats d'analyse (COA)

Lot/Batch Number
SHBS9779
SHBS6214
SHBS4410
SHBR4547
SHBS2752

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Systematic studies on the breakdown of p,p'-DDT in tobacco smokes. Presence of methyl chloride, dichloromethane, and chloroform in tobacco smokes.
Chopra NM and Sherman LR.
Analytical Chemistry, 44(6), 1036-1038 (1972)
Engineering of ultra-small diagnostic nanoprobes through oriented conjugation of single-domain antibodies and quantum dots.
Sukhanova A, et al.
Protocol Exchange (2012)
Kinetics and Mechanism of the Photooxidation of Bis (bipyridine) dichlororuthenium (II) and the Photoreduction of Bis (bipyridine) dichlororuthenium (III) in Chloroform.
Sathiyabalan S and Hoggard PE.
Inorganic Chemistry, 34(18), 4562-4571 (1995)
The affinity of two antimicrobial peptides derived from bovine milk proteins for model lipid membranes.
Barzyk W, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 343(1), 104-110 (2009)
Eagleson M.
Concise Encyclopedia Chemistry, 216-216 (1994)
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