≥95% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
1,4-Dibromo-2,3-butanediol reacts with aqueous alkaline sodium arsenite to yield mixture of DL-2,3,4-trihydroxybutylarsonic acid and DL-2,3-dihydroxybutane-1,4-bis(arsonic acid).
1,4-Dibromo-2,3-butanediol has been used in the preparation of diquaternary gemini surfactants.
| Pubchem Sid | 488187128 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488187128 |
| Canonical Smiles | C(C(C(CBr)O)O)Br |
| IUPAC Name | 1,4-dibromobutane-2,3-diol |
| InChIKey | XOWDQAHYPSENAC-UHFFFAOYSA-N |
| INCHI | 1S/C4H8Br2O2/c5-1-3(7)4(8)2-6/h3-4,7-8H,1-2H2 |
| Isomeric SMILES | C(C(C(CBr)O)O)Br |
| WGK Germany | 3 |
| PubChem CID | 98512 |
| Molecular Weight | 247.91 |
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 |
| Class | Halohydrins |
| Subclass | Bromohydrins |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bromohydrins |
| Alternative Parents | Secondary alcohols 1,2-diols Organobromides Hydrocarbon derivatives Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary alcohol - Bromohydrin - 1,2-diol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organobromide - Alkyl halide - Alkyl bromide - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as bromohydrins. These are alcohols substituted by a bromine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups. |
| 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 |
|---|---|---|---|
 B2311188 | Certificate of Analysis | Nov 08, 2024 | W131889 |
| B2311132 | Certificate of Analysis | Nov 08, 2024 | W131889 |
| B2311124 | Certificate of Analysis | Nov 01, 2024 | W131889 |
| B2311155 | Certificate of Analysis | Nov 01, 2024 | W131889 |
| B2311172 | Certificate of Analysis | Nov 01, 2024 | W131889 |
| B2311197 | Certificate of Analysis | Nov 01, 2024 | W131889 |
| K2104076 | Certificate of Analysis | Aug 07, 2023 | W131889 |
| K2104077 | Certificate of Analysis | Aug 07, 2023 | W131889 |
| K2104431 | Certificate of Analysis | Aug 07, 2023 | W131889 |
| Melt Point(°C) | 82-84°C |
|---|---|
| Molecular Weight | 247.910 g/mol |
| XLogP3 | 0.500 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 247.887 Da |
| Monoisotopic Mass | 245.889 Da |
| Topological Polar Surface Area | 40.500 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 52.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Caifeng Wei, Zujing Yang, Jianyong Zhang, Hongbing Ji. (2022) Selective and efficient removal of ReO4- from aqueous solution by imidazolium-based porous organic polymers. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, [PMID:] [10.1016/j.colsurfa.2022.129754] |
