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5-Hydroxy-1-tetralone

CAS No.
28315-93-7
Chemical Name:
5-Hydroxy-1-tetralone
Synonyms
5-hydroxy-3,4-dihydronaphthalen-1(2H)-one;1-TETRALON-5-OL;5-Hydroxy-1-tetraL;5-HYDROY-1-TETRAIONE;5-HYDROXY-1-TETRALONE;5-Hydroxy-α-tetralone;5-Hydroxy-1-tetrazole;Levobunolol Impurity 5;5-Hydroxytetralin-1-one;5-hydroxy-1-oxotetraline
CBNumber:
CB8111979
Molecular Formula:
C10H10O2
Molecular Weight:
162.19
MDL Number:
MFCD00001693
MOL File:
28315-93-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08
Product description Number Pack Size Price
5-Hydroxy-1-tetralone 99% 219975 5g $53.7
5-Hydroxy-1-tetralone >99.0%(GC) H0614 1g $57
5-Hydroxy-1-tetralone >99.0%(GC) H0614 5g $175
5-Hydroxy-1-tetralone TRC-H957850-5G 5g $91
5-Hydroxy-1-tetralone TRC-H957850-25G 25g $353
More product size

5-Hydroxy-1-tetralone 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
pka 9.37±0.20(Predicted)
color White to Off-White
BRN 2437410
InChI InChI=1S/C10H10O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1,3,5,11H,2,4,6H2
InChIKey YPPZCRZRQHFRBH-UHFFFAOYSA-N
SMILES C1(=O)C2=C(C(O)=CC=C2)CCC1
CAS DataBase Reference 28315-93-7(CAS DataBase Reference)
FDA UNII 8605DD71BS
NIST Chemistry Reference 5-Hydroxy-1-tetralone(28315-93-7)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE Eyeshields, Gloves, type N95 (US)
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
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

5-Hydroxy-1-tetralone price More Price(67)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 219975 5-Hydroxy-1-tetralone 99% 28315-93-7 5g $53.7 2026-04-30 Buy
TCI Chemical H0614 5-Hydroxy-1-tetralone >99.0%(GC) 28315-93-7 1g $57 2026-04-30 Buy
TCI Chemical H0614 5-Hydroxy-1-tetralone >99.0%(GC) 28315-93-7 5g $175 2026-04-30 Buy
TRC TRC-H957850-5G 5-Hydroxy-1-tetralone 28315-93-7 5g $91 2026-06-03 Buy
TRC TRC-H957850-25G 5-Hydroxy-1-tetralone 28315-93-7 25g $353 2026-06-03 Buy
Product number Packaging Price Buy
219975 5g $53.7 Buy
H0614 1g $57 Buy
H0614 5g $175 Buy
TRC-H957850-5G 5g $91 Buy
TRC-H957850-25G 25g $353 Buy

5-Hydroxy-1-tetralone Chemical Properties,Uses,Production

Chemical Properties

light yellow to beige or pinkish crystalline

Uses

5-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.

Synthesis

1,5-Dihydroxy naphthalene

83-56-7

5-Hydroxy-1-tetralone

28315-93-7

The general procedure for the synthesis of 5-hydroxy-1-tetralone from 1,5-dihydroxynaphthalene is as follows: Example 1-1 Method A Preparation of [5-(biphenyl-4-sulfonylamino)-5,6,7,8-tetrahydronaphthalen-1-yloxy]-acetic acid; Synthesis of 5-hydroxy-3,4-dihydro-2H-naphthalen-1-one To a mixed solution of isopropanol (150 mL) and aqueous sodium hydroxide (40 mL) containing 1,5-dihydroxynaphthalene (25.0 g, 156 mmol) was added 10% palladium carbon catalyst (3.9 g) at room temperature. The reaction mixture was transferred to a Parr autoclave (Parr Instrument Company) and reacted at 80 °C for 20 h under 100 psi hydrogen pressure. Upon completion of the reaction, the mixture was cooled to room temperature, filtered through a diatomaceous earth pad (diatomaceous earth filter from World Minerals Inc.) and the filter cake was washed with isopropanol (200 mL). The combined filtrates were treated with activated carbon at 50 °C for 1 h and subsequently filtered through a Celite pad (diatomaceous earth filter). Isopropanol was removed by distillation under reduced pressure and the pH was adjusted to about 2 by slowly adding concentrated hydrochloric acid to the remaining solution, at which point a solid precipitated. The solid product was collected, washed with water (100 mL x 2), and then dried under high vacuum at 50 °C to afford 5-hydroxy-3,4-dihydro-2H-naphthalen-1-one (15.0 g, 60% yield) as a dark brown solid, which can be used in subsequent steps without further purification. Mass spectrometry analysis: calculated value (C10H10O2) 162, measured value (M+H)+ 163.

References

[1] Russian Journal of Organic Chemistry, 2000, vol. 36, # 10, p. 1474 - 1477
[2] Patent: US2010/41714, 2010, A1. Location in patent: Page/Page column 18
[3] Patent: US2010/41760, 2010, A1. Location in patent: Page/Page column 7; 23-24
[4] Journal of Organic Chemistry, 2017, vol. 82, # 18, p. 9844 - 9850

83-56-7
28315-93-7
Synthesis of 5-Hydroxy-1-tetralone from 1,5-Dihydroxy naphthalene
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View Lastest Price from 5-Hydroxy-1-tetralone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
5-Hydroxy-1-tetralone pictures 2026-07-15 5-Hydroxy-1-tetralone
28315-93-7
$29.00 99.75% 10g TargetMol Chemicals Inc.
5-Hydroxy-1-tetralone pictures 2025-06-27 5-Hydroxy-1-tetralone
28315-93-7
$10.00-30.00 50KG 99% 500000kg Hebei Chuanghai Biotechnology Co., Ltd
5-Hydroxy-1-tetralone pictures 2025-06-20 5-Hydroxy-1-tetralone
28315-93-7
1kg 0.99 20 tons Hebei Yanxi Chemical Co., Ltd.
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 5-hydroxy-1-oxotetraline 1,2,3,4-tetrahydro-5-hydroxynaphthalen-1-one 5-HYDROY-1-TETRAIONE 5-Hydroxy-1-tetralone,99% 3,4-Dihydro-5-hydroxy-1(2H)-naphthalenone 5-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-one 5-Hydroxy-3,4-dihydronaphthalene-1(2H)-one 5-Hydroxytetralin-1-one 3,4-Dihydro-5-Hydroxyl-1(2H)-Naphthalen one 5-Hydroxy-1-Tetralone 1,2,3,4-Tetrahydro-1-oxo-5-hydroxynaphthalene 1,2,3,4-Tetrahydro-5-hydroxynaphthyl-1-one 5-Hydroxy-1,2,3,4-tetrahydronapht 5-Hydroxy-α-tetralone 5-hydroxy-3,4-dihydronaphthalen-1(2H)-one 5-Hydroxy-1-tetrazole 5-Hydroxy-3,4-dihydro-2H-naphthalen-1-one 5-Hydroxy-1-tetralone 99% 5-Hydroxy-1-tetralone> 5-Hydroxy-1-tetraL 5-hydroxy-1-tetrahydronaphthalene ketone Benzoicacid,5-acetyl-7-hydroxy-,methylester 5-Hydroxy-1-tetralone, ≥ 99.0% 5-Hydroxy-1-tetralone, 10 mM in DMSO 5-hydroxy-1-tetrahydronaphthone Levobunolol Impurity 5 28315-93-7 C10H10O2 KETONE Building Blocks C10 Carbonyl Compounds Ketones Organic Building Blocks OLED materials,pharm chemical,electronic C10 Carbonyl Compounds Ketones Aromatics Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals