Determine the necessary mass, volume, or concentration for preparing a solution.
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≥95%, sum of enantiomers for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
product description:
(-)-Linalool is a monoterpene compound mainly found in many essential oils. It shows anti-nociceptive and anti-inflammatory activity.
application:
(-)-Linalool can be used as a reactant in:The enantioselective preparation of ophiobolin sesterterpene via diastereoselective reductive radical cascade cyclization.The total synthesis of (-)-5,6-dihydrocineromycin B via (-)-linalool O-triethylsilyl ether.The total synthesis of pladienolide B analog.
| Pubchem Sid | 488189804 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488189804 |
| Canonical Smiles | CC(=CCCC(C)(C=C)O)C |
| IUPAC Name | (3R)-3,7-dimethylocta-1,6-dien-3-ol |
| InChIKey | CDOSHBSSFJOMGT-JTQLQIEISA-N |
| INCHI | 1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m0/s1 |
| Isomeric SMILES | CC(=CCC[C@](C)(C=C)O)C |
| WGK Germany | 3 |
| RTECS | RG5800000 |
| Molecular Weight | 154.25 |
| Reaxy-Rn | 1362385 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1362385&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 | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyclic monoterpenoids |
| Alternative Parents | Tertiary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyclic monoterpenoid - Tertiary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. |
| External Descriptors | Acyclic monoterpenoids |
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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 | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Mar 13, 2026 | L302318 | |
| Certificate of Analysis | Feb 04, 2026 | L302318 | |
| Certificate of Analysis | Sep 13, 2024 | L302318 | |
| Certificate of Analysis | Sep 13, 2024 | L302318 | |
| Certificate of Analysis | Jul 12, 2024 | L302318 | |
| Certificate of Analysis | Jul 12, 2024 | L302318 | |
| Certificate of Analysis | Jul 12, 2024 | L302318 | |
| Certificate of Analysis | Jul 12, 2024 | L302318 |
| Sensitivity | Light sensitive |
|---|---|
| Freezing Point(°C) | −18±3°, neat |
| Refractive Index | 1.462 |
| Flash Point(°F) | 168.8 °F |
| Flash Point(°C) | 76 °C |
| Boil Point(°C) | 198.5°C |
| Molecular Weight | 154.250 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Exact Mass | 154.136 Da |
| Monoisotopic Mass | 154.136 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 154.000 |
| 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. Jianjun Cheng, Qinghua Chen, Qianshuang Guo, Yongjun Du. (2022) Moth sex pheromones affect interspecific competition among sympatric species and possibly population distribution by modulating pre-mating behavior. Insect Science, 30 (2): (501-516). [PMID:35900899] [10.1111/1744-7917.13099] |
| 2. Zhang Hongfei, Li Weizheng, Luo Qianwen, Yang Lei, Gong Dongfeng, Teng Xiaohui, Guo Xianru, Yuan Guohui. (2018) Fatal Attraction: Ricinus communis Provides an Attractive but Risky Mating Site for Holotrichia parallela Beetles. JOURNAL OF CHEMICAL ECOLOGY, 44 (10): (965-974). [PMID:30116996] [10.1007/s10886-018-0994-5] |
| 3. Han Yan, Wei-Xuan Li, Ying-Lin Zhu, Zhi-Yuan Lin, Dan Chen, Yue Zhang, Hai-Peng Lv, Wei-Dong Dai, De-Jiang Ni, Zhi Lin, Yin Zhu. (2024) Comprehensive comparison of aroma profiles and chiral free and glycosidically bound volatiles in Fujian and Yunnan white teas. FOOD CHEMISTRY, [PMID:38547713] [10.1016/j.foodchem.2024.139067] |
| 4. Yue Chen, Linbo Gou, Di Liu, Shengfang Wu, Xiuwen Zhou, Tai-Ping Fan, Long Wang, Yujie Cai. (2025) Engineering an ATP-saving mevalonate pathway for high-efficiency S-(+)-linalool production in Serratia marcescens. Synthetic and Systems Biotechnology, [PMID:] [10.1016/j.synbio.2025.11.010] |
| 5. Jiarui Tong, Xiangrong Zhu, Xiumei Chen, Nengguo Tao. (2026) Trans-2-hexenal-loaded gelatin/dialdehyde starch/nanocellulose cushioning aerogel: synergistic postharvest preservation of Chinese bayberry with 1-MCP. FOOD RESEARCH INTERNATIONAL, [PMID:41794491] [10.1016/j.foodres.2026.118612] |