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46259

Supelco

1,1,2,2-Tetrachloroethane

analytical standard

Synonym(s):

Acetylene tetrachloride

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About This Item

Linear Formula:
CHCl2CHCl2
CAS Number:
79-34-5
Molecular Weight:
167.85
Beilstein:
969206
EC Number:
201-197-8
MDL number:
MFCD00000848
UNSPSC Code:
41116107
PubChem Substance ID:
329757111
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

5.8 (vs air)

vapor pressure

8 mmHg ( 20 °C)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.494 (lit.)

bp

147 °C (lit.)

mp

−43 °C (lit.)

density

1.586 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-8°C

SMILES string

ClC(Cl)C(Cl)Cl

InChI

1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H

InChI key

QPFMBZIOSGYJDE-UHFFFAOYSA-N

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Application

1,1,2,2-Tetrachloroethane may be used as an extraction solution for the simultaneous determination of chloramphenicol and thiamphenicol in honey samples using dispersive liquid-liquid microextraction followed by high-performance liquid chromatography.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H310 + H330,H411

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Aquatic Chronic 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK4400
BCCK0944
BCCH5973
BCCD5088
BCCB0724

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Dispersive liquid--liquid microextraction followed by high-performance liquid chromatography as an efficient and sensitive technique for simultaneous determination of chloramphenicol and thiamphenicol in honey
Chen H, et al.
Analytica Chimica Acta, 632(1), 80-85 (2009)
Bahngmi Jung et al.
Chemosphere, 71(4), 726-734 (2007-12-11)
Transformation of 1,1,2,2-tetrachloroethane (1,1,2,2-TeCA) by Fe(II) in 10% cement slurries was characterized using a batch reactor system. 1,1,2,2-TeCA was completely converted to trichloroethylene (TCE) within 1h in all experiments, even in controls with cement that did not include Fe(II). Therefore
Maciej Bujak et al.
Chemical communications (Cambridge, England), 47(31), 8769-8771 (2011-05-28)
Directional Cl···Cl type I and II interactions govern the low-density aggregation of 1,1,2,2-tetrachloroethane molecules in synclinal conformation in the crystalline state at low temperature, whereas the dense molecular packing in high-pressure is achieved for the antiperiplanar conformers and electrostatically less
Jiaheng Zhang et al.
Talanta, 88, 330-337 (2012-01-24)
A novel pretreatment method termed ultrasound-assisted dispersive liquid-liquid microextraction (UADLLME) coupled with high-performance liquid chromatography-ultraviolet detector (HPLC-UV) was applied for the detection of four synthesized metabolites of mequindox in pig urine samples. A total volume of 200 μL of methanol
Simona Rossetti et al.
Biotechnology and bioengineering, 100(2), 240-249 (2008-04-24)
An anaerobic microcosm set up with aquifer material from a 1,1,2,2-tetrachloroethane (TeCA) contaminated site and amended with butyrate showed a complete TeCA dechlorination to ethene. A structure analysis of the microbial community was performed by fluorescence in situ hybridization (FISH)
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Protocols

US EPA Method TO-17: GC Analysis of Volatiles on VOCOL® after Collection/Desorption using Air Toxics Tube

US EPA Method TO-17: GC Analysis of Volatiles on VOCOL® after Collection/Desorption using Air Toxics Tube

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

US EPA Method 8260 describes the analysis of volatile organic compounds in solid wastes and ground waters. This application illustrates the analysis of many compounds commonly analyzed by this method using purge and trap coupled to GC-MS.

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