Date published: 2025-12-19

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1,1,1,2-Tetrachloroethane (CAS 630-20-6)

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CAS Number:
630-20-6
Molecular Weight:
167.85
Molecular Formula:
C2H2Cl4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,1,1,2-Tetrachloroethane, also known as methylchloroform, is a nonflammable liquid with a colorless appearance and a distinct chloroform-like odor. This organochloride compound finds extensive use in various industrial and commercial applications. Moreover, it serves as a solvent and reagent in laboratory experiments and plays a role as a cleaning agent within the electronics industry. The versatility of 1,1,1,2-Tetrachloroethane extends to numerous scientific research applications.


1,1,1,2-Tetrachloroethane (CAS 630-20-6) References

  1. Influence of anionic cosolutes and pH on nanoscale zerovalent iron longevity: time scales and mechanisms of reactivity loss toward 1,1,1,2-tetrachloroethane and Cr(VI).  |  Xie, Y. and Cwiertny, DM. 2012. Environ Sci Technol. 46: 8365-73. PMID: 22780331
  2. Chlorinated solvent transformation by palladized zerovalent iron: mechanistic insights from reductant loading studies and solvent kinetic isotope effects.  |  Xie, Y. and Cwiertny, DM. 2013. Environ Sci Technol. 47: 7940-8. PMID: 23755912
  3. Granular Activated Carbon Adsorption of Carcinogenic Volatile Organic Compounds at Low Influent Concentrations.  |  Kempisty, DM., et al. 2020. J Am Water Works Assoc. 1: PMID: 32184496
  4. Merging shuttle reactions and paired electrolysis for reversible vicinal dihalogenations.  |  Dong, X., et al. 2021. Science. 371: 507-514. PMID: 33510026
  5. Reductive Cytochrome P450 Reactions and Their Potential Role in Bioremediation.  |  Behrendorff, JBYH. 2021. Front Microbiol. 12: 649273. PMID: 33936006
  6. Nickel-catalyzed C-O/N-H, C-S/N-H, and C-CN/N-H annulation of aromatic amides with alkynes: C-O, C-S, and C-CN activation.  |  Iyori, Y., et al. 2020. Chem Sci. 12: 1772-1777. PMID: 34163938
  7. [Simultaneous determination of 18 chlorinated hydrocarbon organic solvents in cosmetics by gas chromatography-mass spectrometry].  |  Tang, J., et al. 2021. Se Pu. 39: 324-330. PMID: 34227313
  8. Concise synthesis of N-thiomethyl benzoimidazoles through base-promoted sequential multicomponent assembly.  |  Tian, J., et al. 2019. RSC Adv. 9: 30570-30574. PMID: 35530231
  9. Negative Atmospheric Pressure Chemical Ionization of Chlorinated Hydrocarbons Studied by Ion Mobility Spectrometry (IMS) and IMS-MS Techniques.  |  Moravský, L., et al. 2022. J Am Soc Mass Spectrom. 33: 1569-1576. PMID: 35861584
  10. Enantioselective Inter- and Intramolecular Sulfenofunctionalization of Unactivated Cyclic and (Z)-Alkenes.  |  Matviitsuk, A., et al. 2022. ACS Catal. 12: 7377-7385. PMID: 36686398
  11. Asymmetric synthesis of complex tricyclo[3.2.2.0]nonenes from racemic norcaradienes: kinetic resolution via Diels-Alder reaction.  |  Wang, S., et al. 2023. Chem Sci. 14: 1844-1851. PMID: 36819855
  12. New Model to Predict Infinite Dilution Activity Coefficients Based on (∂p/∂x) T,x → 0.  |  Zheng, J., et al. 2023. ACS Omega. 8: 12439-12444. PMID: 37033839
  13. Smoking is associated with elevated blood level of volatile organic compounds: a population-based analysis of NHANES 2017-2018.  |  Wu, G., et al. 2023. Arch Public Health. 81: 55. PMID: 37055810

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,1,1,2-Tetrachloroethane, 1 g

sc-237641
1 g
$66.00