oxyquinoline
8-hydroxylquinoline

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  BOC Sciences

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  Product(s):
  148-24-3 8-Hydroxyquinoline 95%
  8-Hydroxyquinoline, a monoprotic bidentate chelating agent, has antiseptic, disinfectant, and pesticide propertiesas. And it can be used as the electron-transporting and chromaticity-tuning layer.

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  Glentham Life Sciences Ltd

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  GA0472 8-Hydroxyquinoline

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  Penta International Corporation

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  08-69900 8-HYDROXYQUINOLINE BASE C.P.

Name: quinolin-8-ol CAS Number: 148-24-3 3D/inchi Other(deleted CASRN): 123574-67-4 ECHA EINECS - REACH Pre-Reg: 205-711-1 FDA UNII: 5UTX5635HP Nikkaji Web: J2.960B Beilstein Number: 0114512 MDL: MFCD00006807 XlogP3: 2.00 (est) Molecular Weight: 145.16099000 Formula: C9 H7 N O BioActivity Summary: listing NMR Predictor: Predict (works with chrome, Edge or firefox) Category:cosmetic agents   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: Appearance: white to pale yellow crystalline powder (est) Assay: 95.00 to 100.00 Food Chemicals Codex Listed: No Melting Point: 75.50 °C. @ 760.00 mm Hg Boiling Point: 267.00 °C. @ 760.00 mm Hg Vapor Pressure: 0.001660 mmHg @ 25.00 °C. (est) Flash Point: 290.00 °F. TCC ( 143.10 °C. ) (est) logP (o/w): 2.020 Soluble in:   water, 556 mg/L @ 20 °C (exp)   water, 7965 mg/L @ 25 °C (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: CosIng: cosmetic data Cosmetic Uses: stabilising agents   Suppliers: BOC Sciences For experimental / research use only. 8-Hydroxyquinoline 95% Odor: characteristic Use: 8-Hydroxyquinoline, a monoprotic bidentate chelating agent, has antiseptic, disinfectant, and pesticide propertiesas. And it can be used as the electron-transporting and chromaticity-tuning layer. EMD Millipore For experimental / research use only. 8-Hydroxyquinoline sds Glentham Life Sciences 8-Hydroxyquinoline Penta International 8-HYDROXYQUINOLINE BASE C.P. Santa Cruz Biotechnology For experimental / research use only. 8-Hydroxyquinoline ≥99% Sigma-Aldrich For experimental / research use only. 8-Hydroxyquinoline ACS reagent, 99%   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: oral-guinea pig LD20 1205 mg/kg Teratology, The International Journal of Abnormal Development. Vol. 20, Pg. 413, 1979. unreported-mammal (species unspecified) LD50 1000 mg/kg "Chemistry of Pesticides," Melnikov, N.N., New York, Springer-Verlag New York, Inc., 1971Vol. -, Pg. 410, 1971. intraperitoneal-mouse LD50 43 mg/kg Farmakologiya i Toksikologiya Vol. 42, Pg. 396, 1979. oral-mouse LD50 20000 mg/kg Drugs in Japan Vol. 6, Pg. 271, 1982. oral-rat LD50 1200 mg/kg Pesticide Chemicals Official Compendium, Association of the American Pesticide Control Officials, Inc., 1966. Vol. -, Pg. 602, 1966. Dermal Toxicity: subcutaneous-mouse LD50 83600 ug/kg Pharmazie. Vol. 1, Pg. 150, 1946. Inhalation Toxicity: inhalation-rat LC50 > 1210 mg/m3/6H Journal of the American College of Toxicology. Vol. 11, Pg. 497, 1992.   Safety in Use Information: Category: cosmetic agents Recommendation for oxyquinoline usage levels up to:   not for fragrance use.   Recommendation for oxyquinoline flavor usage levels up to:   not for flavor use.   Safety References: European Food Safety Authority (EFSA) reference(s): Reasoned opinion on the modification of the existing MRL for 8-hydroxyquinoline in tomatoes View page or View pdf Peer review of the pesticide risk assessment of the active substance 8-hydroxyquinoline View page or View pdf Review of the existing maximum residue levels for 8-hydroxyquinoline according to Article 12 of Regulation (EC) No 396/2005 View page or View pdf EPI System: View Daily Med:search Chemical Carcinogenesis Research Information System:Search AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search Carcinogenic Potency Database:Search EPA GENetic TOXicology:Search EPA Substance Registry Services (TSCA):148-24-3 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :1923 National Institute of Allergy and Infectious Diseases:Data WGK Germany:3 quinolin-8-ol Chemidplus:0000148243 EPA/NOAA CAMEO:hazardous materials RTECS:VC4200000 for cas# 148-24-3   References:   quinolin-8-ol NIST Chemistry WebBook: Search Inchi Canada Domestic Sub. List: 148-24-3 Pubchem (cid): 1923 Pubchem (sid): 134975266   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): C19434 HMDB (The Human Metabolome Database): Search Export Tariff Code: 2933.40.7000 ChemSpider: View Wikipedia: View Formulations/Preparations: •usepaopp pesticide code 059803; trade names: fennosan h 30, nci-c55298, tumex, usaf ek-794, quinophenol. •available in usa in technical & reagent grades. it is also available as 0.5% soln (or aerosol) suitable for topical use.   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   not found in nature   Synonyms: oxy benzopyridine   bioquin oxy chinolin 8- chinolinol   fennosan 8- hydroxy quinoline 8- hydroxy-chinolin (8- hydroxy)quinoline 8- hydroxychinolin 8- hydroxylquinoline 8- hydroxyquinolin-n-oxide 8- hydroxyquinoline 1-aza naphthalene-8-ol aza naphthalene-8-ol   oxine   quino phenol 8- quinol   quinolin-8-ol 8-oxy quinoline   quinoline, 8-hydroxy-   quinolinol 8- quinolinol   quinophenol   tumex   Articles:   None found yet. 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Notes: an antiseptic with mild fungistatic, bacteriostatic, anthelmintic, and amebicidal action. it is also used as a reagent and metal chelator, as a carrier for radio-indium for diagnostic purposes, and its halogenated derivatives are used in addition as topical anti-infective agents and oral antiamebics.