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cryptomeridiol
(1R,4aR,7R,8aR)-7-(2-hydroxy-2-propanyl)-1,4a-dimethyldecahydro-1-naphthalenol

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Name:(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol
CAS Number: 4666-84-6Picture of molecule3D/inchi
Other(deleted CASRN):55353-16-7
FDA UNII: Y2KBV9FZ9M
Nikkaji Web:J13.424D
XlogP3-AA:3.00 (est)
Molecular Weight:240.38656000
Formula:C15 H28 O2
BioActivity Summary:listing
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
Boiling Point: 317.30 °C. @ 760.00 mm Hg (est)
Flash Point: 279.00 °F. TCC ( 137.30 °C. ) (est)
logP (o/w): 3.090 (est)
Soluble in:
 water, 67.72 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.
Cryptomeridiol 98%
Odor: characteristic
Use: Cryptomeridiol isolated from the herbs of Blumea balsamifera DC. It exhibits a significant and concentration-dependent inhibitory effect on platelet-activating factor receptor binding. antispasmodic agent;
Coompo
For experimental / research use only.
Cryptomeridiol from Plants ≥96%
 
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 cryptomeridiol usage levels up to:
 not for fragrance use.
 
Recommendation for cryptomeridiol 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 :165258
National Institute of Allergy and Infectious Diseases:Data
(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol
Chemidplus:0004666846
 
References:
 (1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):165258
Pubchem (sid):135122164
 
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
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB38018
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 cymbopogon proximus
Search Trop Picture
 
Synonyms:
(2R-(2alpha,4aalpha,8beta,8abeta))-decahydro-8-hydroxy-alpha,alpha,4a,8-tetramethyl-2-naphthalene methanol
 eudesmane-4a,11-diol
(1R,4aR,7R,8aR)-7-(2-hydroxy-2-propanyl)-1,4a-dimethyldecahydro-1-naphthalenol
(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol
(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyldecahydronaphthalen-1-ol
2-naphthalenemethanol, decahydro-8-hydroxy-a,a,4a,8-tetramethyl-, (2R,4aR,8R,8aR)-
 proximadiol
 

Articles:

PubMed:Melanogenesis inhibitory activity of sesquiterpenes from Canarium ovatum resin in mouse B16 melanoma cells.
PubMed:Inhibitory effect of compounds from Goniothalamus tapis Miq. and Goniothalamus uvaroides King on platelet-activating factor receptor binding.
PubMed:Sesquiterpenes from Blumea balsamifera.
PubMed:[Chemical constituents from Aeschynanthus longicaullis].
PubMed:[Studies on chemical constituents from rhizomes of Hedychium chrysoleucum].
PubMed:Beyerane derivatives and a sesquiterpene dimer from Japanese Cypress (Chamaecyparis obtusa).
PubMed:[Study on the chemical constituents of Buddleja purdomii].
PubMed:Antifungal metabolites from Blumea balsamifera.
PubMed:Chemical-microbiological synthesis of cryptomeridiol derivatives by Gliocladium roseum: semisynthesis of 11-hydroxyeudesmanolides.
PubMed:Cytotoxic constituents of the fruits of Cananga odorata.
PubMed:Constituents of local plants.
PubMed:An analytical method for proximadiol, the active principle of Cymbopogon proximus.
 
Notes:
dicyclic sesquiterpenediol from cymbopogon proximus with antispasmodic activity.
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