Skip to Content
MilliporeSigma
All Photos(1)

Documents

T19208

Sigma-Aldrich

β-Tetralone

98%

Synonym(s):

beta-Tetralone, 3,4-Dihydro-2(1H)-naphthalenone, 3,4-Dihydro-2-naphthol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C10H10O
CAS Number:
530-93-8
Molecular Weight:
146.19
Beilstein/REAXYS Number:
509386
EC Number:
208-498-3
MDL number:
MFCD00001727
UNSPSC Code:
12352100
PubChem Substance ID:
24899999
NACRES:
NA.22

Quality Level

200

assay

98%

refractive index

n20/D 1.560 (lit.)

bp

131 °C/11 mmHg (lit.)

mp

18 °C (lit.)

density

1.106 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

O=C1CCc2ccccc2C1

InChI

1S/C10H10O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-4H,5-7H2

InChI key

KCKZIWSINLBROE-UHFFFAOYSA-N

Gene Information

human ... CYP2A6(1548)
mouse ... Cyp2a5(13087)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 5

1 of 5

1-Benzosuberone 99%

Sigma-Aldrich

B10587

1-Benzosuberone

1,2-Dihydronaphthalene 95%

Sigma-Aldrich

D105937

1,2-Dihydronaphthalene

1-Indanone ReagentPlus®, ≥99%

Sigma-Aldrich

I2304

1-Indanone

tBuBrettPhos 97%

Sigma-Aldrich

730998

tBuBrettPhos

Cyclohexanone ACS reagent, ≥99.0%

Sigma-Aldrich

398241

Cyclohexanone

R D Mattes et al.
Physiology & behavior, 72(1-2), 217-229 (2001-03-10)
Ethanol is a common dietary constituent, but knowledge of its chemosensory properties and their relationship to its ingestion is limited. Twenty-five male and 25 female, light-regular ethanol consumers participated in five test sessions. Sessions involved determination of taste, olfactory and
H S Shin et al.
Applied microbiology and biotechnology, 57(4), 506-510 (2002-01-05)
Biotransformation of 6-bromo-2-tetralone (Br-beta-tetralone) to 6-bromo-2-tetralol (Br-beta-tetralol) by yeast cells of Trichosporon capitatum (ATCC 74312) and its partially purified Br-beta-tetralone reductase was evaluated in an electrochemical bioreactor. The biotransformation rates and final product formation were significantly affected by substrate concentration
M Goto et al.
Chemical & pharmaceutical bulletin, 48(10), 1529-1531 (2000-10-25)
The reactions of the lithium enolate of 1-tetralone with reactive alkyl halides were examined in the absence and in the presence of 3 eq of various ligands for the lithium. It is shown that the rates of the reactions are
Palladium-catalyzed asymmetric allylic alkylation of alpha-aryl ketones.
Barry M Trost et al.
Angewandte Chemie (International ed. in English), 41(18), 3492-3495 (2002-09-26)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service