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castoryl maleate
modified castor oil in which some of the unsaturation has been converted to a cyclic dicarboxylic acid

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CAS Number: 241153-84-4Picture of molecule3D/inchi
FDA UNII: V5B97ZYP2F
XlogP3-AA:18.10 (est)
Molecular Weight:1031.50622000
Formula:C61 H106 O12
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:cosmetic ingredient for skin conditioning
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.167e-018 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
 
Suppliers:
Jiangyin Healthway
Castoryl Maleate
New functional food ingredients
M.C.Biotec
Castoryl Maleate
Odor: characteristic
Use: Castoryl maleate is a lipid analogue with good affinity to the skin and superior moisturization on wash off Lipids found in healthy, moisturized skin are typically in a lamellar gel crystalline state that is responsible for the skin's barrier function. In the stratum corneum, ceramides and cholesterol organize together with fatty acids to form the highly ordered lipid phase of the skin. Rinse-off personal cleansing products designed to remove dirt and debris from the skin can also remove protective lipids, which can weaken the skin's natural defensive barrier and result in dry, flaky skin. Even emollient-rich cleansers can leave the skin feeling and looking dry, since most emollients are washed away when the cleanser is rinsed off. Castoryl maleate has been found not only to deposit onto the skin from rinse-off cleansing formulas, but also to deliver quantifiable long-lasting moisturization. When combined with palmitic acid, it forms a highly ordered lamellar gel that is analogous to the lipid barrier in healthy skin, and can duplicate in-vitro the effect of the more expensive, complex combination of cholesterol and sphingosine ceramide. Skin texture and appearance are visibly improved.
 
Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
cosmetic ingredient for skin conditioning
Recommendation for castoryl maleate usage levels up to:
 not for fragrance use.
 
Recommendation for castoryl maleate flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
National Institute of Allergy and Infectious Diseases:Data
(Z)-4-[(Z)-18-[2,3-bis[[(Z)-12-hydroxyoctadec-9-enoyl]oxy]propoxy]-18-oxooctadec-9-en-7-yl]oxy-4-oxobut-2-enoic acid
Chemidplus:0241153844
 
References:
 (Z)-4-[(Z)-18-[2,3-bis[[(Z)-12-hydroxyoctadec-9-enoyl]oxy]propoxy]-18-oxooctadec-9-en-7-yl]oxy-4-oxobut-2-enoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (sid):172649798
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):Search
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 castor oil maleate
 castor oil, monomaleate
(Z)-4-[(Z)-18-[2,3-bis[[(Z)-12-hydroxyoctadec-9-enoyl]oxy]propoxy]-18-oxooctadec-9-en-7-yl]oxy-4-oxobut-2-enoic acid
 modified castor oil in which some of the unsaturation has been converted to a cyclic dicarboxylic acid
 ricinoleyl monomaleate triglyceride
 
 
Notes:
None found
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