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219975

Sigma-Aldrich

5-Hydroxy-1-tetralone

99%

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About This Item

Empirical Formula (Hill Notation):
C10H10O2
CAS Number:
28315-93-7
Molecular Weight:
162.19
Beilstein:
2437410
EC Number:
248-958-0
MDL number:
MFCD00001693
UNSPSC Code:
12352100
PubChem Substance ID:
24853157
NACRES:
NA.22

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

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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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

219975-VAR:
219975-BULK:
219975-5G:
219975-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ3562
MKBP6931V
MKBC3741V
MKBC3741
07729BJ

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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)
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)
M Tanaka et al.
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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