Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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≥99% 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 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
4-Bromobenzyl alcohol undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls. It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde. It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.
4-Bromobenzyl alcohol was used in the synthesis of: hydroxyl end functionalized, substituted polyfluorene amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)
| Pubchem Sid | 488184478 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184478 |
| Canonical Smiles | C1=CC(=CC=C1CO)Br |
| IUPAC Name | (4-bromophenyl)methanol |
| InChIKey | VEDDBHYQWFOITD-UHFFFAOYSA-N |
| INCHI | 1S/C7H7BrO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2 |
| Isomeric SMILES | C1=CC(=CC=C1CO)Br |
| WGK Germany | 3 |
| Molecular Weight | 187.03 |
| Beilstein | 1931620 |
| Reaxy-Rn | 1931620 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1931620&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 | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzyl alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzyl alcohols |
| Alternative Parents | Bromobenzenes Aryl bromides Primary alcohols Organobromides Hydrocarbon derivatives Aromatic alcohols |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzyl alcohol - Halobenzene - Bromobenzene - Aryl halide - Aryl bromide - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Organobromide - Organohalogen compound - Alcohol - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzyl alcohols. These are organic compounds containing the phenylmethanol substructure. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Dec 05, 2025 | B139372 | |
| Certificate of Analysis | Oct 14, 2025 | B139372 | |
| Certificate of Analysis | Feb 07, 2025 | B139372 | |
| Certificate of Analysis | Feb 07, 2025 | B139372 | |
| Certificate of Analysis | Jan 17, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Jan 09, 2025 | B139372 | |
| Certificate of Analysis | Aug 07, 2023 | B139372 | |
| Certificate of Analysis | Mar 14, 2023 | B139372 | |
| Certificate of Analysis | Jun 15, 2022 | B139372 | |
| Certificate of Analysis | Jun 17, 2021 | B139372 | |
| Certificate of Analysis | Jun 17, 2021 | B139372 |
| Solubility | dioxane: soluble1 g/10 mL, clear to faintly turbid, colorless to faintly yellow |
|---|---|
| Melt Point(°C) | 75-77°C |
| Molecular Weight | 187.030 g/mol |
| XLogP3 | 2.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 185.968 Da |
| Monoisotopic Mass | 185.968 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 77.000 |
| 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. Siyuan Chang, Sen Zhang, Tianyi Chen, Lei Xu, Sumin Ge, Bingfeng Li, Chenke Yun, Guoxin Zhang, Xuejun He, Xin Pan. (2023) Efficient synthesis of 5-hydroxymethyl-2-furancarboxylic acid from bio-based high-concentration 5-hydroxymethylfurfural via highly tolerant aldehyde dehydrogenase. Molecular Catalysis, [PMID:] [10.1016/j.mcat.2023.112966] |
| 2. Xiu-Zhi Wei, Fentahun Wondu Dagnaw, Jianguo Liu, Longlong Ma. (2022) Highly selective photocatalytic oxidation of alcohols under the application of novel metal organic frameworks (MOFs) based catalytic system. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:36063631] [10.1016/j.jcis.2022.08.119] |
| 3. Fangshu Xing, Renyou Zeng, Chuchu Cheng, Qiuwen Liu, Caijin Huang. (2022) POM-incorporated ZnIn2S4 Z-scheme dual-functional photocatalysts for cooperative benzyl alcohol oxidation and H2 evolution in aqueous solution. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2022.121087] |
| 4. Shen Tieyin, Zhong Mingjun, Feng Lijuan, Sui Zhuyin, Chen Qi. (2021) Noble metal nanoparticles supported on MOF nanorods and their catalytic applications. JOURNAL OF POROUS MATERIALS, 29 (1): (97-102). [PMID:] [10.1007/s10934-021-01148-3] |
| 5. Yujie Song, Hao Wang, Shijing Liang, Yan Yu, Liuyi Li, Ling Wu. (2018) One-pot synthesis of secondary amine via photoalkylation of nitroarenes with benzyl alcohol over Pd/monolayer H1.07Ti1.73O4·H2O nanosheets. JOURNAL OF CATALYSIS, [PMID:] [10.1016/j.jcat.2018.02.005] |
| 6. Zhang Guofu, Zhang Guihua, Lei Jie, Li Shasha, Xu Shengjun, Ding Chengrong, Shan Shang. (2016) Aerobic alcohol ammoxidation catalyzed by copper(I)/amino acid: a scalable protocol to nitriles. CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 32 (4): (586-593). [PMID:] [10.1007/s40242-016-6067-9] |
| 7. Xin Pan, Yanan Zhu, Yongchang Yang, Qianqian Zhu. (2024) Nitrogen-Doped Porous Carbon Derived from Covalent Triazine Framework for Catalytic Oxidation of Benzyl Alcohol. Nanomaterials, 14 (9): (744). [PMID:38727338] [10.3390/nano14090744] |
| 8. Huan Chen, Yan Zhao, Zhe Zhang, Bo Niu, Yayun Zhang, Donghui Long. (2025) Axial pyridine coordination-induced Co d-orbital rearrangement boosts peroxymonosulfate activation for singlet oxygen evolution in water remediation. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2025.125873] |
| 9. Ye Meng, Jinshu Huang, Jie Li, Yumei Jian, Song Yang, Hu Li. (2023) Enzyme-mimicking single atoms enable selectivity control in visible-light-driven oxidation/ammoxidation to afford bio-based nitriles. GREEN CHEMISTRY, 25 (11): (4453-4462). [PMID:] [10.1039/D3GC00968H] |
| 10. Li Suiqin, Wang Shibin, Wang Yuhang, He Jiahui, Li Kai, Gerken James B., Stahl Shannon S., Zhong Xing, Wang Jianguo. (2025) Synergistic enhancement of electrochemical alcohol oxidation by combining NiV-layered double hydroxide with an aminoxyl radical. Nature Communications, 16 (1): (1-14). [PMID:39747151] [10.1038/s41467-024-55616-w] |
| 11. Chuanshun Feng, Shuo Chen, Linjie Guan, Guoen Zhang, Feng Lin, Qicheng Zhang, Xiaobin Fan, Wenchao Peng, Yang Li. (2025) Internal electric field drives barrier-free singlet oxygen generation on metal-free carbon for dual environmental-organic synthesis applications. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2025.126299] |
| 12. Shaodong Zhai, Xianglong Hu, Yongjun Hu, Baoyan Wu, Da Xing. (2017) Visible light-induced crosslinking and physiological stabilization of diselenide-rich nanoparticles for redox-responsive drug release and combination chemotherapy. BIOMATERIALS, [PMID:28068593] [10.1016/j.biomaterials.2017.01.002] |