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· · COA & SDS available for every product · Same-day shipping on in-stock items Nopol - ≥98%, mixture of isomers , CAS No.128-50-7
GRADE & PURITY ≥98% mixture of isomers Synonyms
Nopol|128-50-7|Homomyrtenol|Nopol (terpene)|Bicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-dimethyl-|6,6-Dimethyl-2-norpinene-2-ethanol|2-NORPINENE-2-ETHANOL, 6,6-DIMETHYL-|6,6-Dimethyl-2-(2-hydroxyethyl)-2-norpinene|Bicyclo(3.1.1)hept-2-ene-2-ethanol, 6,6-dimet
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Why this grade ≥98%, mixture of isomers for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
Nopol | 128-50-7 | Homomyrtenol | Nopol (terpene) | Bicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-dimethyl- | 6,6-Dimethyl-2-norpinene-2-ethanol | 2-NORPINENE-2-ETHANOL, 6,6-DIMETHYL- | 6,6-Dimethyl-2-(2-hydroxyethyl)-2-norpinene | Bicyclo(3.1.1)hept-2-ene-2-ethanol, 6,6-dimet
Specifications & Purity
≥98%, mixture of isomers
Names and Identifiers Canonical Smiles CC1(C2CC=C(C1C2)CCO)C IUPAC Name 2-(6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl)ethanol InChIKey ROKSAUSPJGWCSM-UHFFFAOYSA-N INCHI 1S/C11H18O/c1-11(2)9-4-3-8(5-6-12)10(11)7-9/h3,9-10,12H,4-7H2,1-2H3 Isomeric SMILES CC1(C2CC=C(C1C2)CCO)C Molecular Weight 166.26 Reaxy-Rn 1937743 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1937743&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Lipids and lipid-like molecules Class Prenol lipids Subclass Monoterpenoids Intermediate Tree Nodes Not available Direct Parent Bicyclic monoterpenoids Alternative Parents Primary alcohols Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Pinane monoterpenoid - Bicyclic monoterpenoid - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - 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 Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 166.260 g/mol XLogP3 2.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 2 Exact Mass 166.136 Da Monoisotopic Mass 166.136 Da Topological Polar Surface Area 20.200 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 215.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 2 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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