Description

IUPAC Name: (1R,2R,4aS,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol

InChI: InChI=1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15-,16+,18-,19-,20+/m0/s1

InChIKey: XVULBTBTFGYVRC-HHUCQEJWSA-N

Canonical SMILES: CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C

Isomeric SMILES: C[C@]12CCCC([C@@H]1CC[C@@]([C@@H]2CC[C@](C)(C=C)O)(C)O)(C)C

Synonyms: Sclareol; 515-03-7; labd-14-ene-8,13-diol; (13R)-Labd-14-ene-8,13-diol; Sclareol (natural); (1R,2R,4aS,8aS)-1-((R)-3-hydroxy-3-methylpent-4-en-1-yl)-2,5,5,8a-tetramethyldecahydronaphthalen-2-ol; SCAREOL; UNII-B607NP0Q8Y; …

Botanical Source: Salvia sclarea L.

Product Overview

High-purity Sclareol (Labd-14-ene-8,13-diol), a natural labdane diterpenoid isolated from Salvia sclarea, manufactured to exceptional standards for pharmaceutical and fragrance research.

Technical Specifications

• Molecular Formula: C₂₀H₃₆O₂
• Molecular Weight: 308.50 g/mol
• Purity: ≥98% (HPLC)
• Appearance: White to off-white crystalline powder
• Solubility: Freely soluble in organic solvents

Key Features & Benefits

• Natural diterpene compound
• Sweet, balsamic scent
• Validated chemical structure
• Comprehensive Certificate of Analysis
• Full spectroscopic characterization

Research Applications

1. Pharmaceutical Research

   • Anticancer studies
   • Apoptosis induction research
   • Leukemic cell studies
   • Colon cancer investigations

2. Biomedical Studies

   • Anti-microbial research
   • Antifungal studies
   • Plant metabolite investigations
   • Drug development screening

3. Fragrance Development

   • Amber fragrance synthesis
   • Perfumery applications
   • Aroma compound research

Storage & Handling

• Store at the recommended temperature
• Protect from light and moisture
• Jojoba oil compatibility validated
• Solution preparation guidelines provided

Quality Assurance

• GMP-compliant manufacturing
• Rigorous quality control
• Complete analytical documentation
• Traceable lot numbers
• Stability monitoring program

Research Support

BIORLAB provides:

• Technical consultation
• Analytical method support
• Stability data
• Custom synthesis options
• Application Guidance

Key Physical Properties

• Melting Point: 95-105°C
• Amber colored solid
• Sweet, balsamic scent
• Natural bioactive compound

Research Highlights

1. Cancer Research Applications

   • Human leukemic cell studies
   • Colon cancer cell investigations
   • Apoptosis induction mechanisms

2. Bioavailability Studies

   • Transdermal absorption confirmed
   • Liver accumulation studies
   • Safety profile established

This premium-grade Sclareol is specifically designed for research institutions and pharmaceutical companies advancing therapeutic development and scientific research.

For research and development purposes only. Not for human consumption or clinical use.

[Contact BIORLAB’s technical support team for detailed specifications and custom requirements]