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219975

5-Hydroxy-1-tetralone

Name: 5-Hydroxy-1-tetralone
Brand: ALDRICH

99%

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₀O₂

CAS Number:

28315-93-7

Molecular Weight:

162.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24853157

EC Number:

248-958-0

Beilstein/REAXYS Number:

2437410

MDL number:

MFCD00001693

Assay:

99%

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Properties

Quality Level

100

assay

99%

mp

206-209 °C (lit.)

functional group

ketone

SMILES string

Oc1cccc2C(=O)CCCc12

InChI

1S/C10H10O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1,3,5,11H,2,4,6H2

InChI key

YPPZCRZRQHFRBH-UHFFFAOYSA-N

Description

Application

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Fluorometric detection of glycosphingolipids on thin-layer chromatographic plates.

K Watanabe et al.

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.

Valderrama JA, et al.

Synthetic Communications, 22(4), 629-640 (1992)

A new chiral oxathiane: synthesis, resolution and absolute configuration determination by vibrational circular dichroism.

Solladie-Cavallo A, et al.

Tetrahedron Asymmetry, 12(18), 2605-2611 (2001)

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Global Trade Item Number

SKU	GTIN
219975-5G	04061831810127