5-Hydroxy-1-tetralone

5-Hydroxy-1-tetralone Basic information
Product Name:5-Hydroxy-1-tetralone
Synonyms:1(2H)-Naphthalenone, 3,4-dihydro-5-hydroxy-;3,4-dihydro-5-hydroxy-1(2h)-naphthalenon;5-Hydroxy-3,4-dihydro-1(2H)-naphthalenone;5-HYDROXY-1,2,3,4-TETRAHYDRONAPHTHALEN-1-ONE;5-HYDROXY-1-TETRALONE;1-TETRALON-5-OL;1,2,3,4-tetrahydro-5-hydroxynaphthalen-1-one;5-HYDROY-1-TETRAIONE
CAS:28315-93-7
MF:C10H10O2
MW:162.19
EINECS:248-958-0
Product Categories:OLED materials,pharm chemical,electronic;C10;Carbonyl Compounds;Ketones;Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals
Mol File:28315-93-7.mol
5-Hydroxy-1-tetralone Structure
5-Hydroxy-1-tetralone Chemical Properties
Melting point 206-209 °C (lit.)
Boiling point 228.88°C (rough estimate)
density 1.0281 (rough estimate)
refractive index 1.5380 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in alcohol, ether, benzene and acetic acid.
form Solid
pka9.37±0.20(Predicted)
color White to Off-White
BRN 2437410
CAS DataBase Reference28315-93-7(CAS DataBase Reference)
NIST Chemistry Reference5-Hydroxy-1-tetralone(28315-93-7)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-37/39-26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29145090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
5-Hydroxy-1-tetralone Usage And Synthesis
Chemical Propertieslight yellow to beige or pinkish crystalline
Uses5-Hydroxy-1-tetralone, is used as a metabolite of Levobunolol (L335000) and d-Bunolol (L335010). It is also used as a reagent for the determination of hexoses and oligosaccharides by a fluorescence technique. A reagent that is used for fluorescence determination of enzyme activity. Some of the other applications include as internal standard during HPLC determination of 4-hydroxymephenytoin (4-OH-M) in human urine, as fluorescent labeling reagent during micro detection of glycosphingolipid on TLC plates, in synthesis of 1,2,3,4-tetrahydro-5H-1-benzazepine-quinone derivatives, in synthesis of new chiral oxathiane.
CHEMBRDG-BB 9070835 5-Methoxy-3,4-dihydro-2H-naphthalen-1-one Tetrahydro napyradiomycin C2 napyradiomycin C1 Nanaomycin E Hydroxy silicone oil napyradiomycin B1 1-ACETOXY-8-HYDROXY-1,4,4A,9A-TETRAHYDROANTHRAQUINONE STEFFIMYCIN B 10-Hydroxycamptothecin Levobunolol hydrochloride 2,3-DIHYDRO-9,10-DIHYDROXY-1,4-ANTHRACENEDIONE WS 009B RUGULOSIN napyradiomycin A1 RUBROSKYRIN CHLOROPHOSPHONAZO III

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