≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application：
1,2,3-Tribromobenzene is an organic chemical reagent used in the synthesis of cis-trikentrin B as well as in the synthesis of diphenyl ethers for induction of CYP1A via the receptor mediated pathway.
| Pubchem Sid | 488181446 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181446 |
| Canonical Smiles | C1=CC(=C(C(=C1)Br)Br)Br |
| IUPAC Name | 1,2,3-tribromobenzene |
| InChIKey | GMVJKSNPLYBFSO-UHFFFAOYSA-N |
| INCHI | 1S/C6H3Br3/c7-4-2-1-3-5(8)6(4)9/h1-3H |
| Isomeric SMILES | C1=CC(=C(C(=C1)Br)Br)Br |
| PubChem CID | 11842 |
| Molecular Weight | 314.8 |
| Reaxy-Rn | 2043617 |
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 | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Halobenzenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bromobenzenes |
| Alternative Parents | Aryl bromides Organobromides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Bromobenzene - Aryl halide - Aryl bromide - Hydrocarbon derivative - Organobromide - Organohalogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as bromobenzenes. These are organic compounds containing a bromine atom attached to a benzene ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 E2308172 | Certificate of Analysis | Feb 05, 2026 | T405024 |
| K2229597 | Certificate of Analysis | Sep 16, 2025 | T405024 |
| K2229596 | Certificate of Analysis | Sep 16, 2025 | T405024 |
| K2229578 | Certificate of Analysis | Sep 16, 2025 | T405024 |
| K2229577 | Certificate of Analysis | Sep 16, 2025 | T405024 |
| K2229575 | Certificate of Analysis | Sep 16, 2025 | T405024 |
| C2508110 | Certificate of Analysis | Sep 07, 2022 | T405024 |
| Solubility | Soluble in Toluene |
|---|---|
| Boil Point(°C) | 283 °C |
| Melt Point(°C) | 88 °C |
| Molecular Weight | 314.800 g/mol |
| XLogP3 | 4.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 313.776 Da |
| Monoisotopic Mass | 311.778 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 84.300 |
| 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. You Tao, Tian-Xiong Wang, Xuesong Ding, Bao-Hang Han. (2023) Porous polycarbazole materials prepared by ionothermal synthesis method for carbon dioxide adsorption and electrochemical capacitors. JOURNAL OF POLYMER SCIENCE, [PMID:] [10.1002/pol.20220601] |
