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Thermo Scientific Chemicals
1,10-Decanediol, 97%
CAS: 112-47-0 | C10H22O2 | 174.284 g/mol
化学物質識別子
CAS112-47-0
IUPAC Namedecane-1,10-diol
Molecular FormulaC10H22O2
InChI KeyFOTKYAAJKYLFFN-UHFFFAOYSA-N
SMILESOCCCCCCCCCCO
さらに表示
スペックシート1,10-Decanediol is an minor intermediate in the production of polyesters. It also used in essence, perfumes and in pharmaceuticals. The diacrylate is hydrophobic and used for flexible dental materials, radiation curable coatings, and for lenses.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1,10-Decanediol is an minor intermediate in the production of polyesters. It also used in essence, perfumes and in pharmaceuticals. The diacrylate is hydrophobic and used for flexible dental materials, radiation curable coatings, and for lenses.
Solubility
Soluble in alcohol. Insoluble in water, petroleum ether.
Notes
Store in a cool, dry, well-ventilated area. Incompatible with oxidizing agent.
1,10-Decanediol is an minor intermediate in the production of polyesters. It also used in essence, perfumes and in pharmaceuticals. The diacrylate is hydrophobic and used for flexible dental materials, radiation curable coatings, and for lenses.
Solubility
Soluble in alcohol. Insoluble in water, petroleum ether.
Notes
Store in a cool, dry, well-ventilated area. Incompatible with oxidizing agent.
RUO – Research Use Only
General References:
- Li Li, Zhi-Cheng Tan; Shuang-He Meng; Yong-Ji Song. Final report on the safety assessment of Isobutylparaben and Isopropylparaben. Thermochimica Acta. 1995, 14 (5), 364-372.
- M. J. Diamond; T. H. Applewhite. Alkaline cleavage of hydroxy unsaturated fatty acids and derivatives. II 10-hydroxydecanoic acid from ricinoleates and 1,10-decanediol from ricmoleyl alcohol. Journal of the American Oil Chemist’s Society. 1967, 44 (11), 656-658.