Trichloroethylene - Standard for GC, ≥99.5%(GC), stabilized with 40ppm diisopropylamine , CAS No.79-01-6

CAS: 79-01-6 Cat. No.: T100714 Summenformel: C₂HCl₃ Molekulargewicht: 131.39 Beilstein Registry Number: 1736782 EG-Nummer: 201-167-4 PubChem CID: 6575

GRADE & PURITY Standard for GC, ≥99.5%(GC), stabilized with 40ppm diisopropylamine

Synonyms

1,1,2-Trichloroethene | Triasol | Triol | Nialk | Trielina [Italian] | Ethinyl trichloride | TRICHLOROETHYLENE | TRICHLOROETHYLENE (13C2) | Trilene TE-141 | 1-Chloro-2,2-dichloroethylene | Germalgene | Trichlooretheen | Trichloride, Ethinyl | 1,2,2-Trichl

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Shipped In

FedEx DG Service

Specifications

Synonyme

1,1,2-Trichloroethene | Triasol | Triol | Nialk | Trielina [Italian] | Ethinyl trichloride | TRICHLOROETHYLENE | TRICHLOROETHYLENE (13C2) | Trilene TE-141 | 1-Chloro-2,2-dichloroethylene | Germalgene | Trichlooretheen | Trichloride, Ethinyl | 1,2,2-Trichl

Spezifikationen & Reinheit

Standard for GC, ≥99.5%(GC), stabilized with 40ppm diisopropylamine

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Verschickt in

FedEx DG Service

Note

Standard for GC

Reinheit

≥99.5%(GC)

Namen und Kennungen

Pubchem Sid

508811543

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811543

Kanonisches Lächeln

C(=C(Cl)Cl)Cl

IUPAC Name

1,1,2-trichloroethene

InChIKey

XSTXAVWGXDQKEL-UHFFFAOYSA-N

INCHI

1S/C2HCl3/c3-1-2(4)5/h1H

Isomere SMILES

C(=C(Cl)Cl)Cl

WGK Deutschland

3

RTECS

KX4550000

PubChem CID

6575

UN-Nummer

1710

Verpackungsgruppe

III

Molekulargewicht

131.39

Beilstein

1736782

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Klasse Vinyl halides
      • Subclass Vinyl chlorides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Klasse: Vinyl halides
• Subclass: Vinyl chlorides
• Intermediate Tree Nodes: Not available
• Direct Parent: Vinyl chlorides
• Alternative Parents: Chloroalkenes Organochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Chloroalkene - Haloalkene - Vinyl chloride - Hydrocarbon derivative - Organochloride - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as vinyl chlorides. These are vinyl halides in which a chlorine atom is bonded to an sp2-hybridised carbon atom.
• External Descriptors: a small molecule

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CXCL8 Tchem Interleukin-8 (642 Activities)

Discover Target: CXCL8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CASP1 Tchem Caspase-1 (6235 Activities)

Discover Target: CASP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2E1 Tchem Cytochrome P450 2E1 (2174 Activities)

Discover Target: CYP2E1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

Discover Target: PMP22

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

Aspergillus nidulans (364 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Brechungsindex: 1.476-1.478
• Siedepunkt (°C): 87°C
• Schmelzpunkt (°C): -86°C
• Molekulargewicht: 131.380 g/mol
• XLogP3: 2.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 129.914 Da
• Monoisotopic Mass: 129.914 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 42.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1