loliolid
2(4H)-benzofuranone, 5,6,7,7a-tetrahydro-6-hydroxy-4,4,7a-trimethyl-, (6S,7aR)-

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  CODE138434 CODE138434
  Product(s):
  5989-02-6 Loliolide 98%
  Loliolide is a germination inhibitor that is isolated from Sargassum ringgoldi

Name: (6S,7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one CAS Number: 5989-02-6 3D/inchi FDA UNII: U3BB4IM281 Nikkaji Web: J16.007E XlogP3-AA: 1.00 (est) Molecular Weight: 196.24612000 Formula: C11 H16 O3 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: 352.70 °C. @ 760.00 mm Hg (est) Flash Point: 309.00 °F. TCC ( 153.70 °C. ) (est) logP (o/w): 0.610 (est) Soluble in:   water, 3.333e+004 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. Loliolide 98% Odor: characteristic Use: Loliolide is a germination inhibitor that is isolated from Sargassum ringgoldi Coompo For experimental / research use only. Loliolid from Plants ≥98%   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 loliolid usage levels up to:   not for fragrance use.   Recommendation for loliolid 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 :100332 National Institute of Allergy and Infectious Diseases:Data (6S,7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one Chemidplus:0005989026   References:   (6S,7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one NIST Chemistry WebBook: Search Inchi Pubchem (cid): 100332 Pubchem (sid): 135057462   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 HMDB (The Human Metabolome Database): Search FooDB: FDB004536 VCF-Online: VCF Volatile Compounds in Food ChemSpider: View Wikipedia: View EFSA Update of results on the monitoring of furan levels in food: Read Report EFSA Previous report: Results on the monitoring of furan levels in food: Read Report EFSA Report of the CONTAM Panel on provisional findings on furan in food: Read Report   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   kelp wakame kelp Search Trop Picture   sunflower flower Search Trop Picture   tea leaf oil Search Trop Picture   Synonyms: 2(4H)- benzofuranone, 5,6,7,7a-tetrahydro-6-hydroxy-4,4,7a-trimethyl-, (6S-cis)- 2(4H)- benzofuranone, 5,6,7,7a-tetrahydro-6-hydroxy-4,4,7a-trimethyl-, (6S,7aR)- 1,3- dihydroxy-3,5,5-trimethyl cyclohexylidene-4-acetic acid lactone 1,3- dihydroxy-3,5,5-trimethylcyclohexylidene-4-acetic acid lactone (6S,7aR)-6- hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one (6S,7aR)-6- hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one   loliolide (6S-cis)-5,6,7,7a- tetrahydro-6-hydroxy-4,4,7a-2(4H)-benzofuranone   Articles: PubMed:[Isolation and NMR-study of loliolid from Plantago lanceoata using a displacement reagent].

Notes: None found