≥97% 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.
10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine.[1] It may also be used in the synthesis of : . 10-(methylsulfinyl)decanoic acid . 10-cyanodecanoic acid . (10-oxo-10-(4-(3-thioxo-3H-1,2-dithiol-5-yl)phenoxy)-decyl)triphenylphosphonium bromide . 11-thiastearic acid
| Pubchem Sid | 488188149 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488188149 |
| Sorrisi canonici | C(CCCCC(=O)O)CCCCBr |
| IUPAC Name | 10-bromodecanoic acid |
| InChIKey | PGVRSPIEZYGOAD-UHFFFAOYSA-N |
| INCHI | 1S/C10H19BrO2/c11-9-7-5-3-1-2-4-6-8-10(12)13/h1-9H2,(H,12,13) |
| Isomeri SMILES | C(CCCCC(=O)O)CCCCBr |
| WGK Germania | 3 |
| Peso molecolare | 251.16 |
| Beilstein | 2(4)1055 |
| Reaxy-Rn | 1765027 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1765027&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 | Lipids and lipid-like molecules |
| Classe | Fatty Acyls |
| Subclass | Fatty acids and conjugates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Medium-chain fatty acids |
| Alternative Parents | Halogenated fatty acids Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Medium-chain fatty acid - Halogenated fatty acid - Straight chain fatty acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organobromide - Organohalogen compound - Alkyl halide - Organic oxygen compound - Alkyl bromide - Carbonyl group - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. |
| External Descriptors | Halogenated fatty acids |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 C23211196 | Certificate of Analysis | Sep 03, 2026 | C118560 |
| C23211195 | Certificate of Analysis | Sep 03, 2026 | C118560 |
| C2609636 | Certificate of Analysis | Mar 11, 2026 | C118560 |
| K2122047 | Certificate of Analysis | May 09, 2025 | C118560 |
| K2120176 | Certificate of Analysis | May 09, 2025 | C118560 |
| K2120168 | Certificate of Analysis | May 09, 2025 | C118560 |
| C1805086 | Certificate of Analysis | Apr 09, 2025 | C118560 |
| C1805085 | Certificate of Analysis | Apr 09, 2025 | C118560 |
| L2203388 | Certificate of Analysis | Jan 14, 2025 | C118560 |
| L2203314 | Certificate of Analysis | Sep 18, 2024 | C118560 |
| L2203384 | Certificate of Analysis | Sep 18, 2024 | C118560 |
| L2203385 | Certificate of Analysis | Sep 18, 2024 | C118560 |
| L2203386 | Certificate of Analysis | Sep 18, 2024 | C118560 |
| L2203389 | Certificate of Analysis | Sep 18, 2024 | C118560 |
| L2203391 | Certificate of Analysis | Sep 18, 2024 | C118560 |
| H2005156 | Certificate of Analysis | Mar 08, 2024 | C118560 |
| H2005155 | Certificate of Analysis | Mar 08, 2024 | C118560 |
| Solubilità | Partly miscible in water. |
|---|---|
| Sensibilità | air sensitive |
| Punto di fusione (°C) | 38-41°C |
| Peso molecolare | 251.160 g/mol |
| XLogP3 | 4.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 9 |
| Exact Mass | 250.057 Da |
| Monoisotopic Mass | 250.057 Da |
| Topological Polar Surface Area | 37.300 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 126.000 |
| 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. Guoqiang Lu, Hengda Yuan, Jiulei Zhou, Fuping Chen, Chao Li, Tanlong Xue, Xin Shu, Yingying Zhao, Jun Nie, Xiaoqun Zhu. (2022) Patterned Magnetofluids via Magnetic Printing and Photopolymerization for Multifunctional Flexible Electronic Sensors. ACS Applied Materials & Interfaces, [PMID:35730674] [10.1021/acsami.2c04755] |
| 2. Tianlin Wang, Yue Zheng, Guangren Yu, Xiaochun Chen. (2021) Glycolysis of polyethylene terephthalate: Magnetic nanoparticle CoFe2O4 catalyst modified using ionic liquid as surfactant. EUROPEAN POLYMER JOURNAL, [PMID:] [10.1016/j.eurpolymj.2021.110590] |
| 3. Li Cui, Ren Gao, Qiaowei Zhang, Kun Jiang, Hongyan He, Wei-Lu Ding, Fangqin Cheng. (2024) Benzo-15-Crown-5 Functionalized Ionic Liquids with Enhanced Stability for Effective Separation of Lithium Isotopes: The Effect of Alkyl Chain Length. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.3c05171] |
| 4. Shuo Wang, Yi-Ming Gu, Jin Zhou, Shu-Dong Wang. (2025) Preparation and evaluation of versatile zwitterionic mixed-mode chromatographic stationary phases. JOURNAL OF CHROMATOGRAPHY A, [PMID:40367850] [10.1016/j.chroma.2025.466024] |
