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Key Documents

47794

Supelco

1,2,3-Trichloropropane

analytical standard

Synonyme(s) :

Glycerol trichlorohydrin, Trichlorohydrin

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About This Item

Formule linéaire :
CH2ClCHClCH2Cl
Numéro CAS:
Poids moléculaire :
147.43
Numéro Beilstein :
1732068
Numéro CE :
Numéro MDL:
Code UNSPSC :
12000000
ID de substance PubChem :

Qualité

analytical standard

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 1000 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.484 (lit.)

Point d'ébullition

156 °C (lit.)

Pf

−14 °C (lit.)

Densité

1.387 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

ClCC(Cl)CCl

InChI

1S/C3H5Cl3/c4-1-3(6)2-5/h3H,1-2H2

Clé InChI

CFXQEHVMCRXUSD-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Muta. 2 - Repr. 1B - STOT RE 1 Inhalation

Organes cibles

Kidney,Liver,Mucous membranes

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

165.2 °F - DIN 51758

Point d'éclair (°C)

74 °C - DIN 51758

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificats d'analyse (COA)

Lot/Batch Number

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Consulter la Bibliothèque de documents

Marcin Podsiadło et al.
Acta crystallographica. Section B, Structural science, 62(Pt 6), 1071-1077 (2006-11-17)
The structure of 1,2,3-trichloropropane, ClCH2CHClCH2Cl, in-situ crystallized in a diamond-anvil cell, has been determined by single-crystal X-ray diffraction at 0.28 and 0.35 GPa. A melting point at 295 K and 0.22 GPa has been determined. The molecular conformation of aliphatic
Maryna Lahoda et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 67(Pt 3), 397-400 (2011-03-12)
Haloalkane dehalogenases hydrolyze carbon-halogen bonds in a wide range of halogenated aliphatic compounds. The potential use of haloalkane dehalogenases in bioremediation applications has stimulated intensive investigation of these enzymes and their engineering. The mutant DhaA31 was constructed to degrade the
Martin Klvana et al.
Journal of molecular biology, 392(5), 1339-1356 (2009-07-07)
Eight mutants of the DhaA haloalkane dehalogenase carrying mutations at the residues lining two tunnels, previously observed by protein X-ray crystallography, were constructed and biochemically characterized. The mutants showed distinct catalytic efficiencies with the halogenated substrate 1,2,3-trichloropropane. Release pathways for
J Yan et al.
Environmental microbiology, 11(4), 833-843 (2009-04-28)
Two strictly anaerobic bacterial strains were isolated from contaminated groundwater at a Superfund site located near Baton Rouge, LA, USA. These strains represent the first isolates reported to reductively dehalogenate 1,2,3-trichloropropane. Allyl chloride (3-chloro-1-propene), which is chemically unstable, was produced
Hui Han
Basic & clinical pharmacology & toxicology, 107(6), 988-990 (2010-09-10)
1,2,3-Trichloropropane is widely used in industrial and agricultural production. However 1,2,3-trichloropropane poisoning has been rarely encountered in clinical practices. Here, a 45-year-old farmer who suffered fulminant hepatic failure due to ingestion of 1,2,3-trichloropropane has been reported and literature about 1,2,3-trichloropane

Protocoles

US EPA Method 8260: GC Analysis of Volatiles on SPB®-624 after Purge & Trap using "K" Trap, Fast GC Analysis

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