≥90%(GC) 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Used as a synthetic flavor, as a moth repellent, cold sore topical medication, muscle liniment, and steam-inhaled cough suppressant. It is also used in Used in perfumes.
| Pubchem Sid | 504764031 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504764031 |
| Sourires canoniques | CC1(C2CCC1(C(C2)O)C)C |
| IUPAC Name | (1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol |
| InChIKey | DTGKSKDOIYIVQL-MRTMQBJTSA-N |
| INCHI | 1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1 |
| Isomères SMILES | C[C@@]12CC[C@@H](C1(C)C)C[C@H]2O |
| WGK Allemagne | 2 |
| RTECS | NP7300000 |
| Poids moléculaire | 154.25 |
| Beilstein | 6(2)80 |
| Reaxy-Rn | 6052111 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6052111&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 | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bicyclic monoterpenoids |
| Alternative Parents | Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Bicyclic monoterpenoid - Bornane monoterpenoid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 H2209360 | Certificate of Analysis | Feb 04, 2026 | I138125 |
| H2209366 | Certificate of Analysis | Feb 04, 2026 | I138125 |
| H2209367 | Certificate of Analysis | Feb 04, 2026 | I138125 |
| H2209369 | Certificate of Analysis | Feb 04, 2026 | I138125 |
| A2619146 | Certificate of Analysis | Jan 26, 2026 | I138125 |
| H1611030 | Certificate of Analysis | Oct 14, 2025 | I138125 |
| L2427168 | Certificate of Analysis | Dec 31, 2024 | I138125 |
| Solubilité | Insoluble in water. Soluble in dipropylene glycol, ethyl alcohol (1gm. in 2ml. 70% alcohol). |
|---|---|
| Point d'éclair (°F) | 199.4 °F |
| Point d'éclair (°C) | 93 °C |
| Point de fusion (°C) | 212-214 °C |
| Poids moléculaire | 154.250 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| 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 | 185.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| 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. Shishi Shao, Jiaqiang Zhao, Wei Wang, Hanbing Nie, Yan Jie Li, Xuepeng Zhang, Cheng Zhi Huang, Peng Fei Gao. (2023) Ratiometric room-temperature phosphorescence platform for visual and spectral analysis of naphthalene. SENSORS AND ACTUATORS B-CHEMICAL, [PMID:] [10.1016/j.snb.2023.135047] |
| 2. Xiaoming Zeng, Hao He, Liejiang Yuan, Haizhi Wu, Cong Zhou. (2024) Determination of 24 Trace Aromatic Substances in Rosemary Hydrosol by Dispersed Liquid–Liquid Microextraction–Gas Chromatography. Processes, 12 (3): (498). [PMID:] [10.3390/pr12030498] |
| 3. Miao Liang, Runhu Xin, Wei Guan, Yuping Liu. (2024) Effect of moisture loss on aroma profile, key odorants, and fatty acids of Amomum tsaoko during vacuum oven drying. FOOD CHEMISTRY, [PMID:39674017] [10.1016/j.foodchem.2024.142421] |
| 4. Yan Yang, Siying Liu, Yan Wang, Qin Yang, Baoan Wang, Yuting Zhang, Zaikang Tong, Junhong Zhang. (2025) Antifungal mechanisms of Phoebe bournei wood essential oil against Botryosphaeria dothidea and its application in apples. POSTHARVEST BIOLOGY AND TECHNOLOGY, [PMID:] [10.1016/j.postharvbio.2025.113703] |
| 5. Shijie Xu, Ying Li, Xingsheng Wan, Mingen Fei, Wendi Liu, Renhui Qiu. (2026) Sustainable 4D printing of bio-based shape memory polymer composites derived from isoborneol–thioctic acid with photothermal actuation. COMPOSITES COMMUNICATIONS, [PMID:] [10.1016/j.coco.2026.102807] |
