Determine the necessary mass, volume, or concentration for preparing a solution.
≥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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application:
3,4-Dimethylbenzyl alcohol was used in determination of toxicities of pseudocumene and its metabolites for E.coli JM101.
| Pubchem Sid | 488182824 |
|---|---|
| Canonical Smiles | CC1=C(C=C(C=C1)CO)C |
| IUPAC Name | (3,4-dimethylphenyl)methanol |
| InChIKey | OKGZCXPDJKKZAP-UHFFFAOYSA-N |
| INCHI | 1S/C9H12O/c1-7-3-4-9(6-10)5-8(7)2/h3-5,10H,6H2,1-2H3 |
| Isomeric SMILES | CC1=C(C=C(C=C1)CO)C |
| Molecular Weight | 136.19 |
| Reaxy-Rn | 1929695 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1929695&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 | o-Xylenes Primary alcohols Hydrocarbon derivatives Aromatic alcohols |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | O-xylene - Xylene - Benzyl alcohol - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen 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 | a small molecule |
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 | Aug 15, 2025 | D331591 | |
| Certificate of Analysis | Aug 11, 2025 | D331591 | |
| Certificate of Analysis | Aug 11, 2025 | D331591 | |
| Certificate of Analysis | Aug 11, 2025 | D331591 |
| Boil Point(°C) | 218-221℃ |
|---|---|
| Melt Point(°C) | 62-65℃ |
| Molecular Weight | 136.190 g/mol |
| XLogP3 | 1.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 136.089 Da |
| Monoisotopic Mass | 136.089 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 101.000 |
| 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. 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] |