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

1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one
7H-2,4a-methanonaphthalen-7-one, 1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-

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CAS Number: 23747-14-0Picture of molecule3D/inchi
Other(deleted CASRN):17015-42-8
ECHA EINECS - REACH Pre-Reg:245-859-4
FDA UNII: Search
Nikkaji Web:J242.663C
XlogP3-AA:3.60 (est)
Molecular Weight:218.33954000
Formula:C15 H22 O
NMR Predictor:Predict (works with chrome, Edge 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
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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 316.00 °C. @ 760.00 mm Hg (est)
Flash Point: 283.00 °F. TCC ( 139.30 °C. ) (est)
logP (o/w): 3.422 (est)
Soluble in:
 water, 13.02 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Foreverest Resources
Isolongifolenone 95%
Odor: characteristic
Use: Isolongifolenone, appears white or pale green crystal or powder, has light smell like Camphor with woody and amber odor. Production of fully oxidized with oxygen in the reactor by Isolongifolene, synthesise in the process of filtering, distillation and crystallization. The other method is used Cobalt Acetate as the catalyst, through the processing of distillation, crystallization, filtration.
Foreverest Resources
Isolongifolenone 98%
Odor: characteristic
Use: Isolongifolenone, appears white or pale green crystal or powder, has light smell like Camphor with woody and amber odor. Production of fully oxidized with oxygen in the reactor by Isolongifolene, synthesise in the process of filtering, distillation and crystallization. The other method is used Cobalt Acetate as the catalyst, through the processing of distillation, crystallization, filtration.
 
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:
information only not used for fragrances or flavors
Recommendation for 1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one usage levels up to:
 not for fragrance use.
 
Recommendation for 1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-7H-2,4a-methanonaphthalen-7-one flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
EPA Substance Registry Services (TSCA):23747-14-0
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :90971
National Institute of Allergy and Infectious Diseases:Data
Chemidplus:0023747140
 
References:
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):90971
Pubchem (sid):135049525
 
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
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
isolongifolen-9-one
7H-2,4a-methanonaphthalen-7-one, 1,2,3,4,5,6-hexahydro-1,1,5,5-tetramethyl-
2,2,7,7-tetramethyltricyclo[6.2.1.01,6]undec-5-en-4-one
 

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