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47794

Supelco

1,2,3-Trichloropropane

analytical standard

Sinonimo/i:

Glycerol trichlorohydrin, Trichlorohydrin

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About This Item

Formula condensata:
CH2ClCHClCH2Cl
Numero CAS:
96-18-4
Peso molecolare:
147.43
Beilstein:
1732068
Numero CE:
202-486-1
Numero MDL:
MFCD00000946
Codice UNSPSC:
12000000
ID PubChem:
24871430

Grado

analytical standard

Livello qualitativo

100

CdA

current certificate can be downloaded

Confezionamento

ampule of 1000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.484 (lit.)

P. ebollizione

156 °C (lit.)

Punto di fusione

−14 °C (lit.)

Densità

1.387 g/mL at 25 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

ClCC(Cl)CCl

InChI

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

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Applicazioni

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

Pittogrammi

Skull and crossbonesHealth hazard
GHS06,GHS08

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Kidney,Liver,Mucous membranes

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

165.2 °F - DIN 51758

Punto d’infiammabilità (°C)

74 °C - DIN 51758

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
LC25649V
LC22544V
LC18987V
LC11775V
LB98862V

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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
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