11031-45-1

Basic information

• Product Name: SANTALOL
• Synonyms: SANTALOL;2-PENTEN-1-OL, 5-(2,3-DIMETHYL TRICYCLO [2.2.1.0(2,6)] HEPT-3-YL)-2-METHYL;A AND B-SANTALOL;FEMA 3006;SANTALOL ALPHA- AND BETA- FCC;D-ALPHA-SANTALOL;CIS-ALPHA-SANTALOL;2-Methyl-5-((1S,2S,4R)-2-Methyl-3-Methylenebicyclo[2.2.1]heptan-2-yl)pent-2-en-1-ol
• CAS NO: 11031-45-1
• Molecular Formula: C15H24O
• Molecular Weight: 220.35
• EINECS: 234-262-4
• Mol File: 11031-45-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 312°Cat760mmHg
• Flash Point: 116.3°C
• Appearance: /
• Density: 0.968 g/mL at 25 °C(lit.)
• Vapor Pressure: 2.24E-06mmHg at 25°C
• Refractive Index: 1.502
• Storage Temp.: 2-8°C
• CAS DataBase Reference: SANTALOL(CAS DataBase Reference)
• NIST Chemistry Reference: SANTALOL(11031-45-1)
• EPA Substance Registry System: SANTALOL(11031-45-1)

Safety Data

• Hazardous Substances Data: 11031-45-1(Hazardous Substances Data)

Usage

Chemical Properties

Santalol (α- and β-) has a sweet, sandalwood odor.

Occurrence

The stereochemistry of santalols has been discussed by Brieger (Burdock, 1995); santalols are found among the constituents of various sandalwood species (Santalum album L., S. spicatum, S. autrocaledonicum); the α- and β-isomers are present in varying ratios, with the α-isomer usually more abundant.

Uses

Different sources of media describe the Uses of 11031-45-1 differently. You can refer to the following data:
1. Santalol is a naturally occuring sesquiterpene that has antibacterial, anti-hyperglycaemic, anti inflammatory and antioxidant effects with a sweet woody odor making it useful in essential oils.
2. Santalol, α- and β-isomers are used as analytical standards for the quantification of the analytes in fragrances using flow-modulation comprehensive two-dimensional gas chromatography coupled to mass spectrometry (FM GCxGC/MS).
3. Santalol is a flavoring agent that is a colorless or pale yellow liquid, with odor resembling sandalwood. it is soluble in alcohol, fixed oils, mineral oil, and propylene glycol; and insoluble in water and glyc- erin. it is obtained from a sandalwood oil source.

Synthesis

The commercial product is generally a mixture of α- and β-santalol obtained by fractional distillation of sandalwood oil; noncommercial syntheses are known.

InChI:InChI=1/C15H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h2-9,16H,10-15H2,1H3/b3-2+,5-4+,7-6+,9-8+