≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Room temperature Ships FedEx DG Service 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488180104 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180104 |
| Sonrisas canónicas | C(C(Br)Br)(Br)Br |
| IUPAC Name | 1,1,2,2-tetrabromoethane |
| InChIKey | QXSZNDIIPUOQMB-UHFFFAOYSA-N |
| INCHI | 1S/C2H2Br4/c3-1(4)2(5)6/h1-2H |
| Isómeros SMILES | C(C(Br)Br)(Br)Br |
| WGK Alemania | 2 |
| RTECS | KI8225000 |
| PubChem CID | 6588 |
| Número ONU | 2504 |
| Grupo de embalaje | III |
| Peso molecular | 345.65 |
| Beilstein | 1098321 |
| Reaxy-Rn | 1098321 |
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 |
| Clase | Organobromides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organobromides |
| Alternative Parents | Hydrocarbon derivatives Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as organobromides. These are compounds containing a chemical bond between a carbon atom and a bromine atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 E2428371 | Certificate of Analysis | Mar 10, 2026 | T108648 |
| E2428372 | Certificate of Analysis | Mar 10, 2026 | T108648 |
| E2428373 | Certificate of Analysis | Mar 10, 2026 | T108648 |
| E2428385 | Certificate of Analysis | Mar 10, 2026 | T108648 |
| K1710170 | Certificate of Analysis | Jan 08, 2025 | T108648 |
| C2427068 | Certificate of Analysis | Apr 03, 2024 | T108648 |
| H2317040 | Certificate of Analysis | Jul 19, 2023 | T108648 |
| J2119665 | Certificate of Analysis | Jul 19, 2023 | T108648 |
| J2120056 | Certificate of Analysis | Jul 19, 2023 | T108648 |
| K2317056 | Certificate of Analysis | Jul 19, 2023 | T108648 |
| J2119657 | Certificate of Analysis | Jul 19, 2023 | T108648 |
| A2002173 | Certificate of Analysis | Jul 12, 2023 | T108648 |
| J2119660 | Certificate of Analysis | Jul 07, 2023 | T108648 |
| B2307048 | Certificate of Analysis | Feb 22, 2023 | T108648 |
| B2307050 | Certificate of Analysis | Feb 18, 2023 | T108648 |
| B2307054 | Certificate of Analysis | Feb 18, 2023 | T108648 |
| Solubilidad | Insoluble in water; Degree of Solubility in water: 678 mg/l 25 °C; Miscible with Chloroform,Aniline,Ethanol,Ether; Soluble in Benzene,Acetone |
|---|---|
| Sensibilidad | Light sensitive. |
| Índice de refracción | 1.638 |
| Punto de ebullición (°C) | 243.5°C |
| Punto de fusión (°C) | 0°C(lit.) |
| Peso molecular | 345.650 g/mol |
| XLogP3 | 3.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 1 |
| Exact Mass | 345.685 Da |
| Monoisotopic Mass | 341.689 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 26.500 |
| 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. Huaxun Luo, Weida Chen, Jiaming Hu, Feng Zhang, Xingbang Hu. (2023) Highly Selective Oxidation of Toluene to Benzaldehyde in Alkaline Systems. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.3c01049] |
| 2. Chen Lu, Jiaming Hu, Yuning Meng, Aidong Zhou, Feng Zhang, Zhibing Zhang. (2018) The synergistic effect of benzyl benzoate on the selective oxidation of toluene to benzaldehyde. CHEMICAL ENGINEERING RESEARCH & DESIGN, [PMID:] [10.1016/j.cherd.2018.10.019] |
| 3. Siyang Tang, Zhen Liu, Xiaowei Yan, Ning Li, Ruihua Cheng, Xuelian He, Boping Liu. (2014) Kinetic studies on the pyrrole–Cr-based Chevron-Phillips ethylene trimerization catalyst system. APPLIED CATALYSIS A-GENERAL, [PMID:] [10.1016/j.apcata.2014.04.006] |
| 4. Feifan Yin, Murilege Chao, Jinhua Chen, Yanheng Yao, Miao He, Qiufeng Wang, Wenting Cheng, Yongliang Cai, Zhongyun Wang, Yang Xiang. (2025) One-Pot and Enzyme-Free Analysis of mRNA Vaccines Based on a Double Amplification System Featured by Adjustable Structure MNAzyme. ANALYTICAL CHEMISTRY, [PMID:40974015] [10.1021/acs.analchem.5c04634] |
