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Merck

32211-M

Sigma-Aldrich

Chloroform

puriss. p.a., reag. ISO, reag. Ph. Eur., 99.0-99.4% (GC)

Synonim(y):

Methylidyne trichloride, Trichloromethane

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About This Item

Wzór empiryczny (zapis Hilla):
CHCl3
Numer CAS:
Masa cząsteczkowa:
119.38
Beilstein:
1731042
Numer WE:
Numer MDL:
Kod UNSPSC:
12191502
Identyfikator substancji w PubChem:
NACRES:
NA.21

agency

USP/NF
reag. ISO
reag. Ph. Eur.

gęstość pary

4.1 (vs air)

ciśnienie pary

160 mmHg ( 20 °C)

klasa czystości

puriss. p.a.

Próba

99.0-99.4% (GC)

Postać

liquid

zawiera

~1% ethanol as stabilizer

metody

RNA extraction: suitable

zanieczyszczenia

≤0.00001% free chlorine (Cl)
≤0.00005% free acid (as HCl)
≤0.0005% non-volatile matter
≤0.005% aldehydes and ketones (as CH3COCH3)
≤0.005% carbonyl compounds (as CO)
≤0.01% tetrachloroethene (GC)
≤0.01% tetrachloromethane (GC)
≤0.01% trichloroethene (GC)
≤0.01% water (Karl Fischer)
≤0.03% dichloromethane (GC)
0.6-1.0% ethanol (GC)

współczynnik refrakcji

n20/D 1.445 (lit.)

tw

60.5-61.5 °C (lit.)

mp

−63 °C (lit.)

gęstość

1.476-1.483 g/mL at 20 °C
1.492 g/mL at 25 °C (lit.)

ślady anionów

chloride (Cl-): ≤0.0001%

ślady kationów

Al: ≤0.50 ppm
B: ≤0.02 ppm
Ba: ≤0.10 ppm
Ca: ≤0.50 ppm
Cd: ≤0.05 ppm
Co: ≤0.02 ppm
Cr: ≤0.02 ppm
Cu: ≤0.02 ppm
Fe: ≤0.10 ppm
Mg: ≤0.10 ppm
Mn: ≤0.02 ppm
Ni: ≤0.02 ppm
Pb: ≤0.05 ppm
Sn: ≤0.10 ppm
Zn: ≤0.10 ppm

ciąg SMILES

ClC(Cl)Cl

przydatność

complies for appearance
complies for reaction against H2SO4
complies for suitability of determ. w. dithizone

InChI

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

Klucz InChI

HEDRZPFGACZZDS-UHFFFAOYSA-N

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Opis ogólny

Chloroform, a halogenated hydrocarbon, is widely employed as a solvent. Its photochemical degradation has been investigated in the presence of TiO2 aqueous suspensions (wavelength range of 310-380nm).

Zastosowanie

Chloroform may be employed as a solvent for the following studies:
  • Extraction of RNA from plant cells.
  • Preparation of dioleoylphosphatidylcholine (DOPC) solution.
  • Dissolution of 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC).
It may be employed in a rapid quantitative method for the release of periplasmic proteins from bacterial strains.
Chloroform may be used as a solvent to enhance the enantioselectivity of secondary alcohols formed by the borohydride reduction of carbonyl compounds in the presence of optically active ketoiminatocobalt complexes.

Inne uwagi

For information on chloroform miscibility, please visit the following link:
Chloroform Miscibility/Immiscibility Table

Piktogramy

Skull and crossbonesHealth hazard

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Organy docelowe

Central nervous system, Liver,Kidney

Kod klasy składowania

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

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

does not flash

Temperatura zapłonu (°C)

does not flash


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Gurman Singh Pall et al.
Nucleic acids research, 35(8), e60-e60 (2007-04-05)
The northern blot, or RNA gel blot, is a widely used method for the discovery, validation and expression analysis of small regulatory RNA such as small interfering RNA (siRNA), microRNA (miRNA) and piwi-interacting RNA (piRNA). Although it is straightforward and
Jameel A Feshitan et al.
Journal of colloid and interface science, 329(2), 316-324 (2008-10-28)
Microbubbles used as contrast agents for ultrasound imaging, vectors for targeted drug delivery and vehicles for metabolic gas transport require better size control for improved performance. Mechanical agitation is the only method currently available to produce microbubbles in sufficient yields
Z V Leonenko et al.
Biochimica et biophysica acta, 1509(1-2), 131-147 (2000-12-19)
We have used magnetic alternating current mode atomic force microscopy (MAC-AFM) to investigate the formation of supported phospholipid bilayers (SPB) by the method of vesicle fusion. The systems studied were dioleoylphosphatidylcholine (DOPC) on mica and mica modified with 3-aminopropyl-triethoxy-silane (APTES)
G F Ames et al.
Journal of bacteriology, 160(3), 1181-1183 (1984-12-01)
We introduce a method by which periplasmic proteins can be released rapidly, simply, and quantitatively by treating cells with chloroform. All the amino acid-binding proteins tested maintained their activity during chloroform treatment. This method makes practical the analysis of the

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