6073C2A77I 79-54-9 Levopimaric acid 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1theta-(1alpha,4abeta,4balpha,10aalpha))- Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- (8CI) 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R-(1alpha,4abeta, 4balpha,10aalpha))- delta6,8(14)-Abietadienoic acid NSC 4827 beta-Pimaric acid l-Pimaric acid l-Sapietic acid UNII-6073C2A77I CAS 79-54-9

Purity 97%+In StockPharmaceutical Standards
CAS No.79-54-9
Molecular FormulaC20H30O2
Molecular Weight302.45 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6073C2A77I
79-54-9
Levopimaric acid
1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1theta-(1alpha,4abeta,4balpha,10aalpha))-
Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- (8CI)
1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R-(1alpha,4abeta, 4balpha,10aalpha))-
delta6,8(14)-Abietadienoic acid
NSC 4827
beta-Pimaric acid
l-Pimaric acid
l-Sapietic acid
UNII-6073C2A77I CAS 79-54-9 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

6073C2A77I 79-54-9 Levopimaric acid 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1theta-(1alpha,4abeta,4balpha,10aalpha))- Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- (8CI) 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R-(1alpha,4abeta, 4balpha,10aalpha))- delta6,8(14)-Abietadienoic acid NSC 4827 beta-Pimaric acid l-Pimaric acid l-Sapietic acid UNII-6073C2A77I (CAS 79-54-9), molecular formula C20H30O2 and molecular weight 302.45 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 6073C2A77I 79-54-9 Levopimaric acid 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1theta-(1alpha,4abeta,4balpha,10aalpha))- Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- (8CI) 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R-(1alpha,4abeta, 4balpha,10aalpha))- delta6,8(14)-Abietadienoic acid NSC 4827 beta-Pimaric acid l-Pimaric acid l-Sapietic acid UNII-6073C2A77I (C20H30O2) contains a steroid core, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 302.45 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 6073C2A77I 79-54-9 Levopimaric acid 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1theta-(1alpha,4abeta,4balpha,10aalpha))- Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- (8CI) 1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,4b,5,9,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R-(1alpha,4abeta, 4balpha,10aalpha))- delta6,8(14)-Abietadienoic acid NSC 4827 beta-Pimaric acid l-Pimaric acid l-Sapietic acid UNII-6073C2A77I under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC20H30O2
Molecular Weight302.45 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957

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