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SOLANESOL |
| (2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethyl-2,6,10,14,18,22,26,30, 34-Hexatriacontanonaen-1-ol; (2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35- nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol; Other CAS RN: 540-03-4; 15639-69-7; 111820-07-6 |
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| PRODUCT IDENTIFICATION |
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CAS RN |
13190-97-1 |
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EINECS RN |
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FORMULA |
C45H74O |
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MASS |
631.07 |
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CHEMICAL FAMILY |
Unsaturated polyisoprenoid |
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CATEGORY |
Fatty alcohol |
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| PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE |
yellowish crystalline powder |
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MELTING POINT |
35 C |
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BOILING POINT |
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DENSITY |
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SOLUBILITY IN WATER |
Insoluble |
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pH |
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VAPOR DENSITY |
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REFRACTIVE INDEX |
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FLASH POINT |
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| STABILITY AND REACTIVITY | |
| STABILITY | Stable under normal temperatures and pressures |
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INCOMPATIBLE MATERIALS |
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| DECOMPOSITION PRODUCTS |
Carbon monoxide, Carbon dioxide |
| POLYMERIZATION |
Will not occur |
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NFPA RATINGS |
Health: 1; Flammability: 0; Reactivity: 0 |
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| SAFETY |
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HAZARD NOTES |
May cause irritation. May be harmful by inhalation, ingestion, or skin absorption. |
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EYE |
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SKIN |
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INGESTION |
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INHALATION |
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CHRONIC |
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| TRANSPORT & REGULATORY INFORMATION |
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UN NO. |
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| HAZARD CLASS |
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| PACKING GROUP |
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| HAZARD SYMBOL |
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RISK PHRASES |
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SAFETY PHRASES |
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| GENERAL DESCRIPTION & EXTERNAL LINKS |
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wikipedia linking: (http://en.wikipedia.org/wiki/Fatty_alcohol) Long-chain trans-polyprenol (n>8) have been characterized from Eucommia ulmoides. Geraniol (from rose oil) is a monoterpene (2 isoprene units). It has a rose-like odor and is commonly used in perfumes and as several fruit flavors. Geraniol is also an effective mosquito repellent. Inversely, it can attract bees as it is produced by the scent glands of honey bees to help them mark nectar-bearing flowers and locate the entrances to their hives. Farnesol is a sesquiterpene (3 isoprene units). It is the prenol that corresponds to the carbon skeleton of the simplest juvenile hormone described for the first time in insects in 1961 (Schmialek PZ, Z Naturforsch 1961, 16b, 461; Wigglesworth VB, J Insect Physiol 1961, 7, 73). It is present in many essential oils such as citronella, neroli, cyclamen, lemon grass, rose, and others. It is used in perfumery to emphasize the odors of sweet floral perfumes. It is especially used in lilac perfumes. As a pheromone, farnesol is a natural pesticide for mites. Geranylgeraniol is a diterpene (4 isoprene units). Geraniol and geranylgeraniol are important molecules in the synthesis of various terpenes, the acylation of proteins and the synthesis of vitamins (Vitamins E and K). The covalent addition of phosphorylated derivatives of typical isoprenoids, farnesyl pyrophosphate and geranylgeranyl pyrophosphate, to proteins is a process (prenylation) common to G protein subunits. These isoprenylated proteins have key roles in membrane attachment leading to central functionality in cell biology and pathology. Solanesol, discovered in tobacco leaves in 1956 (Rowland RL et al., J Am Chem Soc 1956, 78, 4680), may be an important precursor of the tumorigenic polynuclear aromatic hydrocarbons of smoke but is also a possible side chain for plastoquinone. (http://www.cyberlipid.org/) Solanesol is C45 sesquiterpenoid alcohol abundant in tobacco leaves. It an intermediate of vitamin K2 and coenzyme Q10 and other nutrients. |
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| SALES SPECIFICATION |
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APPEARANCE |
yellowish crystalline powder |
| ASSAY (HPLC) |
90.0% min |
| MELTING POINT |
35 C |
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| PRICE INFORMATION |