![]() 9-Icosanol structure
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Common Name | 9-Icosanol | ||
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CAS Number | 5333-42-6 | Molecular Weight | 298.547 | |
Density | 0.8±0.1 g/cm3 | Boiling Point | 357.7±10.0 °C at 760 mmHg | |
Molecular Formula | C20H42O | Melting Point | -1-1ºC(lit.) | |
MSDS | Chinese USA | Flash Point | 129.7±7.1 °C |
Development of ciclopirox olamine topical formulations: evaluation of drug release, penetration and cutaneous retention.
Pharm. Dev. Technol. 20(2) , 197-203, (2015) With the aim of reducing system absorption and consequently, the side effects, and simultaneously select a penetration enhancing, three topical formulations with 0.5% ciclopirox olamine (CO) and 15% of propylene glycol (PG), ethoxydiglycol or oleic acid were ... |
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The effect of alcohol structures on the interaction mode with the hexameric capsule of resorcin[4]arene.
Chemistry 18(27) , 8515-20, (2012) After more than a century of research on resorcin[4]arenes (1) it is clear that such systems form spontaneously [1(6)(H(2)O)(8)]-type hexameric capsules in wet, non-polar, organic solvents. However, the interactions of these hexameric capsules with alcohols a... |
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Contact sensitivity to octyldodecanol and trometamol in an anti-itch cream.
Contact Dermatitis 56(5) , 289-90, (2007)
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Final report on the safety assessment of Octyidodecyl Stearoyl Stearate.
Int. J. Toxicol. 20 Suppl 3 , 51-9, (2001) Octyldodecyl Stearoyl Stearate functions as an occlusive skin-conditioning agent and as a nonaqueous viscosity-increasing agent in many cosmetic formulations. Current concentrations of use are between 0.7% and 23%, although historically higher concentrations ... |
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Development of topical hydrogels containing genistein-loaded nanoemulsions.
J. Biomed. Nanotechnol. 8(2) , 330-6, (2012) This article describes the development of topical hydrogels containing genistein-loaded nanoemulsions, obtained by means of spontaneous emulsification. This procedure yielded monodisperse nanoemulsions in a sub 250 nm range exhibiting negative zeta-potential ... |
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Airway responsiveness of rabbits after exposure to 2-octyl dodecanol.
AIHA J. (Fairfax,. Va.) 64(4) , 461-6, (2003) Cooling lubricants are used in the metal industry during drilling or turning. Vapors and aerosols of these lubricants are suspected to induce airway hyperresponsiveness (AHR) in exposed workers. In a previous study the authors demonstrated that water-soluble ... |
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Free-choice-profile descriptive analysis of sticks with conditioning agents.
J. Cosmet. Sci. 57(6) , 455-63, (2006) Nine formulations to be used as stick bases were manufactured using sodium stearate, propyleneglycol, and water, adding different concentrations of the following conditioning agents: octyldodecanol, PPG-5-ceteth-20, and PPG-15-stearyl ether. Free-choice-profi... |
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Effects of ethylcellulose and 2-octyldodecanol additives on skin permeation and irritation with ethylene-vinyl acetate copolymer matrix patches containing formoterol fumarate.
Biol. Pharm. Bull. 29(8) , 1717-22, (2006) Skin permeation of formoterol fumarate (FF) and irritation with ethylene-vinyl acetate (EVA) copolymer matrix patches was investigated using rat and human skin in vitro and different species of experimental animal, respectively. Skin permeation of FF increase... |
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Genital swelling caused by octyldodecanol contact dermatitis.
Clin. Exp. Dermatol. 28(2) , 228-9, (2003)
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Extractive recovery of aqueous diamines for bio-based plastics production. Krzyzaniak A, et al.
J. Chem. Technol. Biotechnol. 88(10) , 1937-1945, (2013)
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