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· · COA & SDS available for every product · Same-day shipping on in-stock items Nodosin - ≥99% , CAS No.10391-09-0
Synonyms
AKOS032962396 | HY-N3181 | 11-Deacetylsinuolatin E; NSC 285659; Nodosin (terpene) | NODOSIN | CHEBI:70379 | F92771 | Q27138718 | (1S,4S,8R,9R,12S,13S,14R,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadec
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Why this grade ≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -20°C Ships Ice chest + Ice pads 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.
Overview Nodosin is a diterpenoid isolated from Isodon trichocarpus Kudo and I. Japonicus HARA.
Form:Solid
Specifications Synonyms
AKOS032962396 | HY-N3181 | 11-Deacetylsinuolatin E; NSC 285659; Nodosin (terpene) | NODOSIN | CHEBI:70379 | F92771 | Q27138718 | (1S, 4S, 8R, 9R, 12S, 13S, 14R, 16S)-9, 14-dihydroxy-7, 7-dimethyl-17-methylidene-3, 10-dioxapentacyclo[14.2.1.01, 13.04, 12.08, 12]nonadec
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
Nodosin is a diterpenoid isolated from Isodon trichocarpus Kudo and I. Japonicus HARA.
Storage
Protected from light, Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C IUPAC Name (1S,4S,8R,9R,12S,13S,14R,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione InChIKey WZYJEEIAFBHYJS-SONIPUFESA-N INCHI 1S/C20H26O6/c1-9-10-6-11(21)13-19(7-10,15(9)22)17(24)26-12-4-5-18(2,3)14-16(23)25-8-20(12,13)14/h10-14,16,21,23H,1,4-8H2,2-3H3/t10-,11-,12+,13-,14-,16-,19+,20+/m1/s1 Isomeric SMILES CC1(CC[C@H]2[C@]3([C@@H]1[C@@H](OC3)O)[C@@H]4[C@@H](C[C@@H]5C[C@]4(C(=O)C5=C)C(=O)O2)O)C Alternate CAS 10391-09-0 PubChem CID 10248089 MeSH Entry Terms nodosin Molecular Weight 362.42
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 Terpene lactones Intermediate Tree Nodes Not available Direct Parent Diterpene lactones Alternative Parents Kaurane diterpenoids Delta valerolactones Oxanes Tetrahydrofurans Secondary alcohols Ketones Hemiacetals Cyclic alcohols and derivatives Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic heteropolycyclic compounds Substituents Diterpene lactone - Diterpenoid - Kaurane diterpenoid - Delta valerolactone - Delta_valerolactone - Oxane - Cyclic alcohol - Tetrahydrofuran - Carboxylic acid ester - Hemiacetal - Ketone - Lactone - Secondary alcohol - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Carbonyl group - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. External Descriptors delta-lactone 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 Solubility 125 mg/mL (344.90 mM; ultrasound assisted dissolution,<60 ℃) Sensitivity light sensitive Flash Point(°F) 431.78℉ Flash Point(°C) 222.1℃ Boil Point(°C) 615.3℃ at 760mmHg Molecular Weight 362.400 g/mol XLogP3 1.500 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 0 Exact Mass 362.173 Da Monoisotopic Mass 362.173 Da Topological Polar Surface Area 93.100 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 728.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 8 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
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