pimara-7,15-diene
 
Notes:
None found
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CAS Number: 21561-91-1Picture of molecule3D/inchi
Nikkaji Web: J3.113.735G
XlogP3-AA: 6.80 (est)
Molecular Weight: 272.47504000
Formula: C20 H32
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 0.001413 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: natural substances and extractives
Recommendation for pimara-7,15-diene usage levels up to:
 not for fragrance use.
 
Recommendation for pimara-7,15-diene flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
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EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 102580737
National Institute of Allergy and Infectious Diseases: Data
 (2R,4aR,4bS,8aR)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene
Chemidplus: 0021561911
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References:
 (2R,4aR,4bS,8aR)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 102580737
Pubchem (cas): 21561-91-1
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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
FooDB: FDB001466
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: 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
 picea chihuahuana leaf
Search Trop  Picture
 picea martinezii leaf
Search Trop  Picture
 rice
Search Trop  Picture
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Synonyms:
(2R,4aR,4bS,8aR)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene
9beta-pimara-7,15-diene
7,15-pimaradiene
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Articles:
PubMed: HpDTC1, a Stress-Inducible Bifunctional Diterpene Cyclase Involved in Momilactone Biosynthesis, Functions in Chemical Defence in the Moss Hypnum plumaeforme.
PubMed: Identification of UV-Induced Diterpenes Including a New Diterpene Phytoalexin, Phytocassane F, from Rice Leaves by Complementary GC/MS and LC/MS Approaches.
PubMed: Identification of a degradation intermediate of the momilactone A rice phytoalexin by the rice blast fungus.
PubMed: Simultaneous quantification of diterpenoids in Premna integrifolia using a validated HPTLC method.
PubMed: CYP99A3: functional identification of a diterpene oxidase from the momilactone biosynthetic gene cluster in rice.
PubMed: Functional characterization of the rice kaurene synthase-like gene family.
PubMed: Diterpene cyclases responsible for the biosynthesis of phytoalexins, momilactones A, B, and oryzalexins A-F in rice.
PubMed: Identification of syn-pimara-7,15-diene synthase reveals functional clustering of terpene synthases involved in rice phytoalexin/allelochemical biosynthesis.
PubMed: Microbial transformation of 18-hydroxy-9,13-epi-ent-pimara-7,15-diene by Gibberella fujikuroi.
PubMed: Biosynthesis of rice phytoalexin: enzymatic conversion of 3beta-hydroxy-9beta-pimara-7,15-dien-19,6beta-olide to momilactone A.
PubMed: Diterpenes from Sideritis trojana.
PubMed: The biotransformation of 18-hydroxy-9-epi-ent-pimara-7,15-diene by Gibberella fujikuroi.
PubMed: Biosynthesis of cyclic diterpene hydrocarbons in rice cell suspensions: conversion of 9,10-syn-labda-8(17),13-dienyl diphosphate to 9beta-pimara-7,15-diene and stemar-13-ene.
PubMed: Biosynthesis of rice phytoalexins: identification of putative diterpene hydrocarbon precursors.
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