EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

germanicol

Supplier Sponsors

CAS Number: 465-02-1Picture of molecule3D/inchi
FDA UNII: 7NEX9512DZ
Nikkaji Web:J12.058H
XlogP3-AA:9.40 (est)
Molecular Weight:426.72770000
Formula:C30 H50 O
NMR Predictor:Predict (works with chrome, Edge 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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 9.552e-005 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Germanicol 97.5%
Odor: characteristic
Use: Germanicol is a natural compound isolated from the barks of Lecythis pisonis.
 
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:
natural substances and extractives
Recommendation for germanicol usage levels up to:
 not for fragrance use.
 
Recommendation for germanicol 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
Laboratory Chemical Safety Summary :122857
National Institute of Allergy and Infectious Diseases:Data
(3S,4aR,6aS,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol
Chemidplus:0000465021
 
References:
 (3S,4aR,6aS,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):122857
Pubchem (cas):465-02-1
 
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
CHEMBL:View
KEGG (GenomeNet):C19833
HMDB (The Human Metabolome Database):Search
FooDB:FDB013013
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 vitellaria paradoxa seed
Search Trop Picture
 
Synonyms:
(3S,4aR,6aS,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol
 olean-18-en-3-ol, (3beta)-
 

Articles:

PubMed:Strictly Conserved Residues in Euphorbia tirucalli β-Amyrin Cyclase: Trp612 Stabilizes Transient Cation through Cation-π Interaction and CH-π Interaction of Tyr736 with Leu734 Confers Robust Local Protein Architecture.
PubMed:Germanicol induces selective growth inhibitory effects in human colon HCT-116 and HT29 cancer cells through induction of apoptosis, cell cycle arrest and inhibition of cell migration.
PubMed:Multifunctional oxidosqualene cyclases and cytochrome P450 involved in the biosynthesis of apple fruit triterpenic acids.
PubMed:Cytotoxic biomonitored study of Euphorbia umbellata (Pax) Bruyns.
PubMed:Chemical Constituents of Lecythispisonis (Lecythidaceae)--A New Saponin and Complete 1H and 13C Chemical Shift Assignments.
PubMed:Phytochemical and pharmacological study of Ficus palmata growing in Saudi Arabia.
PubMed:Changes in the triterpenoid content of cuticular waxes during fruit ripening of eight grape (Vitis vinifera) cultivars grown in the Upper Rhine Valley.
PubMed:Klodorone A and klodorol A: new triterpenes from Kleinia odora.
PubMed:[Triterpene compounds of Ainsliaea yunnanensis].
PubMed:Effect of cation-π interactions and steric bulk on the catalytic action of oxidosqualene cyclase: a case study of Phe728 of β-amyrin synthase from Euphorbia tirucalli L.
PubMed:[Chemical constituents of Psammosilene tunicoides and bacteriostatic activity].
PubMed:Triterpenoid profile of flower and leaf cuticular waxes of heather Calluna vulgaris.
PubMed:Isolation and characterization of new ceramides from aerial parts of Lepidaploa cotoneaster.
PubMed:Source correlation of biomarkers in a mangrove ecosystem on Santa Catarina Island in southern Brazil.
PubMed:Synthesis and anti-HIV activity of lupane and olean-18-ene derivatives. Absolute configuration of 19,20-epoxylupanes by VCD.
PubMed:Antibacterial activity of the essential oils of Pistacia lentiscus used in Moroccan folkloric medicine.
PubMed:A new triterpene from Barringtonia asiatica.
PubMed:New triterpenes from Barringtonia asiatica.
PubMed:Antiinflammatory properties of Morus nigra leaves.
PubMed:Occurrence and sources of triterpenoid methyl ethers and acetates in sediments of the cross-river system, southeast Nigeria.
PubMed:Composition of the epicuticular and intracuticular wax layers on Kalanchoe daigremontiana (Hamet et Perr. de la Bathie) leaves.
PubMed:Development of the cuticular wax during growth of Kalanchoe daigremontiana (Hamet et Perr. de la Bathie) leaves.
PubMed:Rapid and enantioselective synthetic approaches to germanicol and other pentacyclic triterpenes.
PubMed:Triterpene synthases from the Okinawan mangrove tribe, Rhizophoraceae.
PubMed:Two new 18-en-oleane derivatives from marine mangrove plant, Barringtonia racemosa.
PubMed:Antitumor and antiinflammatory constituents from Celtis sinensis.
PubMed:Cytotoxic activity of moronic acid and identification of the new triterpene 3,4-seco-olean-18-ene-3,28-dioic acid from Phoradendron reichenbachianum.
PubMed:Arabidopsis thaliana LUP1 converts oxidosqualene to multiple triterpene alcohols and a triterpene diol.
PubMed:Koelpinin-A, B and C--three triterpenoids from Koelpinia linearis.
PubMed:Molluscicidal constituents of Marsypianthes chamaedrys.
PubMed:Triterpenoid compounds from Araujia sericifera B. Effects on the isolated guinea pig ileum.
PubMed:Antiplasmodial triterpene from Vernonia brasiliana.
PubMed:Linear, steroidal, and triterpene esters, and steryl glycosides from Festuca argentina.
PubMed:[Triterpene constituents from Euphorbia nematocypha Hand-Mazz].
 
Notes:
None found
Please share your Comments.
Email Address:
Top of Page Home
Copyright © 1980-2021 The Good Scents Company (tgsc) ™ Disclaimer Privacy Policy