trans-isocarveol
trans-p-mentha-1(7),8-diene-2-ol

Supplier Sponsors

Name: (1S,5R)-2-methylidene-5-prop-1-en-2-ylcyclohexan-1-ol CAS Number: 21391-84-4 3D/inchi FDA UNII: Search Nikkaji Web: J487.297E XlogP3-AA: 2.30 (est) Molecular Weight: 152.23672000 Formula: C10 H16 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 Boiling Point: 227.00 to 228.00 °C. @ 760.00 mm Hg (est) Vapor Pressure: 0.015200 mmHg @ 25.00 °C. (est) Flash Point: 194.00 °F. TCC ( 90.00 °C. ) (est) logP (o/w): 2.420 (est) Soluble in:   water, 319.2 mg/L @ 25 °C (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: None found   Suppliers:   None found   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 trans-isocarveol usage levels up to:   not for fragrance use.   Recommendation for trans-isocarveol 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 :6428442 National Institute of Allergy and Infectious Diseases:Data (1S,5R)-2-methylidene-5-prop-1-en-2-ylcyclohexan-1-ol   References:   (1S,5R)-2-methylidene-5-prop-1-en-2-ylcyclohexan-1-ol NIST Chemistry WebBook: Search Inchi Pubchem (cid): 6428442 Pubchem (sid): 162492474   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: FDB004001 Typical G.C. 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   celery seed Search Trop Picture   chenopodium ambrosioides Search Trop Picture   cymbopogon laniger extract @ 24.00-35.20% Data GC Search Trop Picture   eucalyptus globulus bicostata oil @ 0.97% Data GC Search Trop Picture   eucalyptus globulus maidenii f. muell oil @ 0.94% Data GC Search Trop Picture   eucalyptus globulus oil @ 0.18% Data GC Search Trop Picture   eucalyptus globulus oil rwanda @ 0.05% Data GC Search Trop Picture   eucalyptus globulus pseudoglobulus oil @ 0.59% Data GC Search Trop Picture   fleabane oil (conyza canadensis) @ 0.20% Data GC Search Trop Picture   gingergrass oil @ 12.14% Data GC Search Trop Picture   laurel leaf oil turkey @ 0.30% Data GC Search Trop Picture   layana oil kenya @ trace% Data GC Search Trop Picture   tsauri grass oil @ 17.00% Data GC Search Trop Picture   Synonyms: trans-p- mentha-1(7),8-dien-2-ol trans-para- mentha-1(7),8-dien-2-ol trans-p- mentha-1(7),8-diene-2-ol trans-para- mentha-1(7),8-diene-2-ol trans-1(7),8-p- menthadien-2-ol trans-1(7),8-para- menthadien-2-ol trans-2- methylene-5-isopropyl cyclohexanol trans-2- methylene-5-isopropyl-cyclohexanol trans-2- methylene-5-isopropylcyclohexanol (1S,5R)-2- methylidene-5-(prop-1-en-2-yl)cyclohexanol (1S,5R)-2- methylidene-5-prop-1-en-2-ylcyclohexan-1-ol   Articles: US Patents:3,993,604 - Alicyclic compounds, their use and process for preparing same

Notes: None found

Please share your Comments.
Email Address:
Top of Page | Home