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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Dihydrolanosterol - Moligand™, ≥95% , CAS No.79-62-9
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥95% Synonyms
DTXSID101000181 | Lanost-8-en-3-ol # | 5alpha-Lanost-8-en-3 beta-ol | C05109 | 9H273A8B2X | Dihydrolanosterol | UNII-9H273A8B2X | 24-dihydrolanosterol | Lanost-8-en-3beta-ol | 3beta-Hydroxylanost-8-ene | MBZYKEVPFYHDOH-BQNIITSRSA-N | 24,25-Dihydrolanoster
Storage
Store at 2-8°C,Protected from light
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Why this grade Moligand™, ≥95% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light Ships Wet ice 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.
Vue d’ensemble Dihydrolanosterol is a subtrate of CYP51 and a cholesterol biosynthesis inhibitor.
Specifications Synonymes
DTXSID101000181 | Lanost-8-en-3-ol # | 5alpha-Lanost-8-en-3 beta-ol | C05109 | 9H273A8B2X | Dihydrolanosterol | UNII-9H273A8B2X | 24-dihydrolanosterol | Lanost-8-en-3beta-ol | 3beta-Hydroxylanost-8-ene | MBZYKEVPFYHDOH-BQNIITSRSA-N | 24,25-Dihydrolanoster
Spécifications et pureté
Moligand™, ≥95%
Conditions de stockage de stockage
Store at 2-8°C,Protected from light
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Pubchem Sid 504758733 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504758733 Sourires canoniques CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C IUPAC Name (3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol InChIKey MBZYKEVPFYHDOH-BQNIITSRSA-N INCHI 1S/C30H52O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h20-22,25-26,31H,9-19H2,1-8H3/t21-,22-,25+,26+,28-,29-,30+/m1/s1 Isomères SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@]2([C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C Poids moléculaire 428.73 Reaxy-Rn 45962208 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=45962208&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 Classe Prenol lipids Subclass Triterpenoids Intermediate Tree Nodes Not available Direct Parent Triterpenoids Alternative Parents 3-beta-hydroxysteroids 14-alpha-methylsteroids Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Triterpenoid - 14-alpha-methylsteroid - 3-beta-hydroxysteroid - Hydroxysteroid - 3-hydroxysteroid - Steroid - 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 triterpenoids. These are terpene molecules containing six isoprene units. External Descriptors Cholesterol and derivatives 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Soluble in chloroform (slightly), and ethyl acetate (slightly, heated). Point d'ébullition (°C) 454.33° C (Predicted) Point de fusion (°C) 190.97° C Poids moléculaire 428.700 g/mol XLogP3 9.400 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 5 Exact Mass 428.402 Da Monoisotopic Mass 428.402 Da Topological Polar Surface Area 20.200 Ų Heavy Atom Count 31 Formal Charge 0 Complexity 716.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 7 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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Reconstitution Calculator Avis Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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