calendic acid
 
Notes:
None found
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    • BOC Sciences
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      Product(s):
      28872-28-8 Jacaric acid ≥95%
      Jacaric acid is a conjugated polyunsaturated fatty acid isolated from the seeds of Jacaranda plants. Jacaric acid exhibited imm
       
       
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CAS Number: 28872-28-8Picture of molecule3D/inchi
XlogP3: 6.70 (est)
Molecular Weight: 278.43550000
Formula: C18 H30 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 0.02371 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
Jacaric acid ≥95%
Odor: characteristic
Use: Jacaric acid is a conjugated polyunsaturated fatty acid isolated from the seeds of Jacaranda plants. Jacaric acid exhibited imm
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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
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for calendic acid usage levels up to:
 not for fragrance use.
 
Recommendation for calendic acid flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5282818
National Institute of Allergy and Infectious Diseases: Data
 (8E,10E,12Z)-octadeca-8,10,12-trienoic acid
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References:
 (8E,10E,12Z)-octadeca-8,10,12-trienoic acid
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5282818
Pubchem (cas): 28872-28-8
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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
CHEBI: View
HMDB (The Human Metabolome Database): HMDB30962
FooDB: FDB002944
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 calendula officinalis seed
Search Trop  Picture
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Synonyms:
(8E,10E,12Z)-octadeca-8,10,12-trienoic acid
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Articles:
PubMed: Robust inhibitory effects of conjugated linolenic acids on a cyclooxygenase-related linoleate 10S-dioxygenase: Comparison with COX-1 and COX-2.
PubMed: Induction of apoptosis and inhibition of invasion in choriocarcinoma JEG-3 cells by α-calendic acid and β-calendic acid.
PubMed: Fatty acid composition of lipids in pot marigold (Calendula officinalis L.) seed genotypes.
PubMed: Growth inhibition and apoptosis induction by all-trans-conjugated linolenic acids on human colon cancer cells.
PubMed: Conjugated fatty acids accumulate to high levels in phospholipids of metabolically engineered soybean and Arabidopsis seeds.
PubMed: Lipids as renewable resources: current state of chemical and biotechnological conversion and diversification.
PubMed: Effect of conjugated FA on feed intake, body composition, and liver FA in mice.
PubMed: Mechanism of 1,4-dehydrogenation catalyzed by a fatty acid (1,4)-desaturase of Calendula officinalis.
PubMed: Identification and analysis of a gene from Calendula officinalis encoding a fatty acid conjugase.
PubMed: Formation of conjugated delta8,delta10-double bonds by delta12-oleic-acid desaturase-related enzymes: biosynthetic origin of calendic acid.
PubMed: Isolation and characterization of a calendic acid producing (8,11)-linoleoyl desaturase.
PubMed: Calendic acid in seed oils of the genus Calendula.
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