SMILES string
ClC(CCl)CCl
InChI
1S/C3H5Cl3/c4-1-3(6)2-5/h3H,1-2H2
InChI key
CFXQEHVMCRXUSD-UHFFFAOYSA-N
grade
certified reference material, TraceCERT®
agency
EPA 552
product line
TraceCERT®
CofA
current certificate can be downloaded
feature
standard type internal
packaging
ampule of 1 mL
concentration
200 μg/mL in methanol
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
cleaning products
cosmetics
environmental
food and beverages
personal care
format
single component solution
storage temp.
2-8°C
Quality Level
General description
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
51.8 °F
flash_point_c
11 °C
法规信息
危险化学品
此项目有
Comments on "Degradation of 1,2,3-trichloropropane (TCP): hydrolysis, elimination, and reduction by iron and zinc".
C Noubactep
Environmental science & technology, 44(8), 3197-3197 (2010-03-03)
1,2,3-Trichloropropane.
Report on carcinogens : carcinogen profiles, 12, 426-428 (2011-08-27)
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
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
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
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