≥98% 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
application：
(S)-(+)-2-Heptanol is used as pharmaceutical intermediate.
(S)-(+)-2-Heptanol can be used as a starting material to synthesize:
(S)-(+)-2-benzoyloxyheptane by treating with benzoyl anhydride and Et3N in the presence of DMAP.
(S)-2-(p-toluenesulfonyl)heptane by reacting with p-toluenesulfonyl chloride.
(+)-2-Heptyl acetate by treating with acetyl chloride.
| Pubchem Sid | 488192316 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488192316 |
| Canonical Smiles | CCCCCC(C)O |
| IUPAC Name | (2S)-heptan-2-ol |
| InChIKey | CETWDUZRCINIHU-ZETCQYMHSA-N |
| INCHI | 1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3/t7-/m0/s1 |
| Isomeric SMILES | CCCCC[C@H](C)O |
| WGK Germany | 3 |
| Molecular Weight | 116.2 |
| Reaxy-Rn | 1719088 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1719088&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 |
| Class | Fatty Acyls |
| Subclass | Fatty alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty alcohols |
| Alternative Parents | Secondary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. |
| External Descriptors | Fatty alcohols |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 E2216134 | Certificate of Analysis | Feb 04, 2026 | I137289 |
| E2216135 | Certificate of Analysis | Feb 04, 2026 | I137289 |
| K2109428 | Certificate of Analysis | Aug 12, 2025 | I137289 |
| L1905048 | Certificate of Analysis | Sep 07, 2023 | I137289 |
| Solubility | Soluble in water(3569 mg/L at 25°C). |
|---|---|
| Flash Point(°F) | 147.2 °F |
| Flash Point(°C) | 64 °C |
| Molecular Weight | 116.200 g/mol |
| XLogP3 | 2.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Exact Mass | 116.12 Da |
| Monoisotopic Mass | 116.12 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 43.700 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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. Cao Songshuang, Wu Xiaomei, Ma Baodi, Xu Yi. (2025) Highly Efficient Asymmetric Synthesis of Aliphatic Chiral Secondary Alcohols by Whole Cells of E. coli Co-Expressing Alcohol Dehydrogenase and Glucose Dehydrogenase. CATALYSIS LETTERS, 155 (4): (1-10). [PMID:] [10.1007/s10562-025-04970-5] |
| 2. Baoqing Bai, Shijie Niu, Junnan Li, Bin Feng, Tao Bo, Jinhua Zhang, Ying Zhang, Yukun Yang. (2026) Effects of fermentation with different coarse cereals on antioxidant capacity, flavor profiles and sensory characteristics of Huangjiu. JOURNAL OF CEREAL SCIENCE, [PMID:] [10.1016/j.jcs.2026.104389] |
