lycopersene
psi,psi-carotene, 7,7',8,8',11,11',12,12',15,15'-decahydro-
 
Notes:
biosynthetic product of squalene synthetase.
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CAS Number: 502-62-5Picture of molecule3D/inchi
Nikkaji Web: J12.235A
XlogP3-AA: 15.30 (est)
Molecular Weight: 546.96602000
Formula: C40 H66
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (est)
Soluble in:
 water, 1.077e-014 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:
 None found
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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: information only not used for fragrances or flavors
Recommendation for lycopersene usage levels up to:
 not for fragrance use.
 
Recommendation for lycopersene flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5365816
National Institute of Allergy and Infectious Diseases: Data
 (6E,10E,14E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaene
Chemidplus: 0000502625
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References:
 (6E,10E,14E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaene
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5365816
Pubchem (sid): 135059306
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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
HMDB (The Human Metabolome Database): Search
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
 not found in nature
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Synonyms:
psi,psi-carotene, 7,7',8,8',11,11',12,12',15,15'-decahydro-
7,7',8,8',11,11',12,12',15,15'-decahydro-psi,psi-carotene
(6E,10E,14E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaene
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Articles:
PubMed: Construction of carotenoid biosynthetic pathways using squalene synthase.
PubMed: Oxidation of acyclic terpenoids by Corynebacterium sp.
PubMed: The stereochemistry of trans-phytoene synthesis. Some observations on lycopersene as a carotene precursor and a mechanism for the synthesis of cis- and trans-phytoene.
PubMed: Prelycopersene pyrophosphate and lycopersene. Intermediates in carotene biosynthesis.
PubMed: Biosynthesis of prelycopersene pyrophosphate and lycopersene by squalene synthetase.
PubMed: Lycopersene and prelycopersene pyrophosphate. Intermediates in carotene biosynthesis.
PubMed: Attempts to detect lycopersene formation in yeast.
PubMed: Incorporation of 2-[14C]mevalonic acid into phytoene by isolated chloroplasts.
PubMed: [DEMONSTRATION OF LYCOPERSENE IN HIGHER PLANTS].
PubMed: Studies in carotenogenesis. 30. The problem of lycopersene formation in Neurospora crassa.
PubMed: Studies in carotenogenesis. 29. Attempts to detect lycopersene in higher plants.
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