≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Kanonisches Lächeln | C(Cl)(Cl)(Cl)Br |
|---|---|
| IUPAC Name | bromo(trichloro)methane |
| InChIKey | XNNQFQFUQLJSQT-UHFFFAOYSA-N |
| INCHI | 1S/CBrCl3/c2-1(3,4)5 |
| Isomere SMILES | C(Cl)(Cl)(Cl)Br |
| WGK Deutschland | 3 |
| RTECS | PA5400000 |
| Molekulargewicht | 198.27 |
| Beilstein | 1732543 |
| Reaxy-Rn | 1732543 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732543&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organohalogen compounds |
| Klasse | Alkyl halides |
| Subclass | Halomethanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Halomethanes |
| Alternative Parents | Organochlorides Organobromides Hydrocarbon derivatives Alkyl chlorides Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Halomethane - Hydrocarbon derivative - Organochloride - Organobromide - Alkyl chloride - Alkyl bromide - Aliphatic acyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as halomethanes. These are organic compounds in which at least one of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms. |
| External Descriptors | Not available |
| Löslichkeit | Not miscible or difficult to mix in water. |
|---|---|
| Brechungsindex | 1.506 |
| Siedepunkt (°C) | 104°C |
| Schmelzpunkt (°C) | -6°C |
| Molekulargewicht | 198.270 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 195.825 Da |
| Monoisotopic Mass | 195.825 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 28.400 |
| 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 |
| 1. Linhao Wang, Jia Wei, Jiangkai Huo, Wei Ji, Xiaohui Zhang, Yanan Li, Jiamei Li, Nan Cui, Wenhao Yan, Yuxin Zhao, Jun Li, Ju Wang. (2025) Harnessing Electronically Core-Shell CoFe Alloy-Carbon from Prussian Blue Analogues for Efficient Pollutant Abatement via Peracetic Acid Activation: Dual Reactive Species Generation and Synergistic Mechanisms. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2025.125284] |
| 2. Yu-Zhen Xu, Yu-Le Wang, Yu-Dong Shan, Song-Hai Wu, Yong Liu, Xu Han. (2024) Relay Catalysis for Epoxidation of Cyclohexene by Mg–Mo Bimetallic Oxides and O2 under Solvent-Free Conditions. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.4c01558] |
| 3. Qing-Shuai Zhang, Yu-Le Wang, Li Yue, Yu-Dong Shan, Song-Hai Wu, Yong Liu, Xu Han. (2025) Highly Selective Oxidation of Benzene to Phenol Mediated by KHCO3 in the Bimetallic Mo–Cu/NC-H2O2 System. INORGANIC CHEMISTRY, [PMID:40293284] [10.1021/acs.inorgchem.5c01346] |
| 4. Yu-Le Wang, Songhai Wu, Yu-Zhen Xu, Yu-Dong Shan, Yong Liu, Xu Han. (2025) Importance of surface peroxo species in the epoxidation of cyclohexene by Mo-doped TS-1 and O2 under solvent-free conditions. Catalysis Science & Technology, [PMID:] [10.1039/D5CY01095K] |
| 5. Huan Wang, Weitao Wang, Shuang Yue, Yang Liu, Jiaqi Zhu, Yiqian Yao, Zhen-Hong He. (2025) Construction of MnOₓ catalysts rich in oxygen vacancies for highly selective oxidation of aromatic alcohols: Structure-activity relationship and mechanism study. APPLIED CATALYSIS A-GENERAL, [PMID:] [10.1016/j.apcata.2025.120746] |
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