≥75%(GC), stabilized with MgO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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.
Conformational isomerism of 1-bromo-2-propanol has been investigated by NMR spectroscopy
| Pubchem Sid | 488183104 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183104 |
| Canonical Smiles | CC(CBr)O |
| IUPAC Name | 1-bromopropan-2-ol |
| InChIKey | WEGOLYBUWCMMMY-UHFFFAOYSA-N |
| INCHI | 1S/C3H7BrO/c1-3(5)2-4/h3,5H,2H2,1H3 |
| Isomeric SMILES | CC(CBr)O |
| WGK Germany | 3 |
| RTECS | UA7388000 |
| UN Number | 1993 |
| Packing Group | I |
| Molecular Weight | 138.99 |
| Reaxy-Rn | 1071195 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1071195&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 |
| Class | Halohydrins |
| Subclass | Bromohydrins |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bromohydrins |
| Alternative Parents | Secondary alcohols Organobromides Hydrocarbon derivatives Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary alcohol - Bromohydrin - 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 |
|---|---|---|---|
 L2123256 | Certificate of Analysis | Jul 15, 2025 | B152044 |
| A2515354 | Certificate of Analysis | Jan 03, 2025 | B152044 |
| A2515355 | Certificate of Analysis | Jan 03, 2025 | B152044 |
| B2320118 | Certificate of Analysis | Dec 11, 2024 | B152044 |
| B2320115 | Certificate of Analysis | Dec 10, 2024 | B152044 |
| B2320120 | Certificate of Analysis | Dec 10, 2024 | B152044 |
| I2311232 | Certificate of Analysis | Feb 23, 2023 | B152044 |
| I2311233 | Certificate of Analysis | Feb 23, 2023 | B152044 |
| I2311234 | Certificate of Analysis | Feb 23, 2023 | B152044 |
| Sensitivity | heat sensitive,air sensitive |
|---|---|
| Refractive Index | 1.48 |
| Flash Point(°F) | 109.4 °F |
| Flash Point(°C) | 54°C(lit.) |
| Molecular Weight | 138.990 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 137.968 Da |
| Monoisotopic Mass | 137.968 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 22.900 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Chi Mingfang, Ke Jingwen, Liu Yan, Wei Miaojin, Li Hongliang, Zhao Jiankang, Zhou Yuxuan, Gu Zhenhua, Geng Zhigang, Zeng Jie. (2024) Spatial decoupling of bromide-mediated process boosts propylene oxide electrosynthesis. Nature Communications, 15 (1): (1-8). [PMID:38684683] [10.1038/s41467-024-48070-1] |
