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· · COA & SDS available for every product · Same-day shipping on in-stock items Home Applications Drug Discovery Hydrocortisone 17-valerate - ≥99% , Glucocorticoid receptor agonist, CAS No.57524-89-7, Glucocorticoid receptor agonist Hydrocortisone 17-valerate - ≥99% , Glucocorticoid receptor agonist, CAS No.57524-89-7, Glucocorticoid receptor agonist
Synonyms
(1S,10S,11S,15S,17S,2R,14R)-17-hydroxy-14-(2-hydroxyacetyl)-2,15-dimethyl-5-ox otetracyclo[8.7.0.0<2,7>.0<11,15>]heptadec-6-en-14-yl pentanoate | DTXCID7025633 | HYDROCORTISONE VALERATE [USP MONOGRAPH] | SCHEMBL80603 | NCGC00024016-03 | Hydrocortisone val
Storage
Store at -20°C,Argon charged
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 Store at -20°C,Argon charged 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 Hydrocortisone Valerate has anti-inflammatory, antipruritic and vasoconstrictive properties.
Specifications Synonyms
(1S, 10S, 11S, 15S, 17S, 2R, 14R)-17-hydroxy-14-(2-hydroxyacetyl)-2, 15-dimethyl-5-ox otetracyclo[8.7.0.0<2, 7>.0<11, 15>]heptadec-6-en-14-yl pentanoate | DTXCID7025633 | HYDROCORTISONE VALERATE [USP MONOGRAPH] | SCHEMBL80603 | NCGC00024016-03 | Hydrocortisone val
Specifications & Purity
≥99%
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Glucocorticoid receptor agonist
Product Properties Names and Identifiers Pubchem Sid 504763440 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504763440 Canonical Smiles CCCCC(=O)OC1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)C(=O)CO IUPAC Name [(8S,9S,10R,11S,13S,14S,17R)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] pentanoate InChIKey FZCHYNWYXKICIO-FZNHGJLXSA-N INCHI 1S/C26H38O6/c1-4-5-6-22(31)32-26(21(30)15-27)12-10-19-18-8-7-16-13-17(28)9-11-24(16,2)23(18)20(29)14-25(19,26)3/h13,18-20,23,27,29H,4-12,14-15H2,1-3H3/t18-,19-,20-,23+,24-,25-,26-/m0/s1 Isomeric SMILES CCCCC(=O)O[C@@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)O)C)C(=O)CO PubChem CID 5282494 Molecular Weight 446.58
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 Steroids and steroid derivatives Subclass Hydroxysteroids Intermediate Tree Nodes Not available Direct Parent 21-hydroxysteroids Alternative Parents Gluco/mineralocorticoids, progestogins and derivatives Steroid esters 20-oxosteroids 11-beta-hydroxysteroids 3-oxo delta-4-steroids Delta-4-steroids Alpha-acyloxy ketones Cyclohexenones Alpha-hydroxy ketones Cyclic alcohols and derivatives Carboxylic acid esters Secondary alcohols Monocarboxylic acids and derivatives Organic oxides Primary alcohols Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Progestogin-skeleton - 21-hydroxysteroid - Pregnane-skeleton - Steroid ester - 20-oxosteroid - 3-oxo-delta-4-steroid - 3-oxosteroid - 11-hydroxysteroid - 11-beta-hydroxysteroid - Oxosteroid - Delta-4-steroid - Cyclohexenone - Alpha-acyloxy ketone - Alpha-hydroxy ketone - Cyclic alcohol - Carboxylic acid ester - Cyclic ketone - Secondary alcohol - Ketone - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Organic oxide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Aliphatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as 21-hydroxysteroids. These are steroids carrying a hydroxyl group at the 21-position of the steroid backbone. External Descriptors glucocorticoid - cortisol ester - valerate ester 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 DMSO: 10 mM ( < 1 mg/ml refers to the product slightly soluble or insoluble ) Melt Point(°C) ~161-163° C Molecular Weight 446.600 g/mol XLogP3 3.800 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 7 Exact Mass 446.267 Da Monoisotopic Mass 446.267 Da Topological Polar Surface Area 101.000 Ų Heavy Atom Count 32 Formal Charge 0 Complexity 832.000 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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