추천 제품
애플리케이션
5-Hydroxy-1-tetralone was used:
- as internal standard during HPLC determination of 4-hydroxymephenytoin (4-OH-M) in human urine
- as fluorescent labeling reagent during microdetection of glycosphingolipid on TLC plates
- in synthesis of 1,2,3,4-tetrahydro-5H-1-benzazepine-quinone derivatives
- in synthesis of new chiral oxathiane
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
A new chiral oxathiane: synthesis, resolution and absolute configuration determination by vibrational circular dichroism.
Tetrahedron Asymmetry, 12(18), 2605-2611 (2001)
Journal of lipid research, 36(8), 1848-1855 (1995-08-01)
A microdetection system for glycosphingolipid analysis has been developed using 5-hydroxy-1-tetralone as the fluorescent labeling reagent. The reagents in H2SO4 permit the fluorometric detection of acidic and neutral glycosphingolipids both in test tube and on thin-layer chromatographic plates. Glycosphingolipids can
Studies on Quinones. Part 22.'Synthesis of 1-Benzazepine-6, 9-Quinone Derivatives.
Synthetic Communications, 22(4), 629-640 (1992)
Journal of chromatography. B, Biomedical applications, 676(1), 87-94 (1996-02-09)
A simple and selective HPLC method for the determination of 4-hydroxymephenytoin (4-OH-M) in human urine, using a controlled potential coulometric detector equipped with a dual working electrode cell of fully porous graphite, has been developed. After acid hydrolysis of urine
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