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95462

Supelco

1,2,3,4-Tetrahydronaphthalene

analytical standard

Synonym(s):

Tetralin solvent

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About This Item

Empirical Formula (Hill Notation):
C10H12
CAS Number:
119-64-2
Molecular Weight:
132.20
Beilstein:
1446407
EC Number:
204-340-2
MDL number:
MFCD00001733
UNSPSC Code:
41116107
PubChem Substance ID:
329770463
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

4.55 (vs air)

vapor pressure

0.18 mmHg ( 20 °C)

Assay

≥99.5% (GC)

autoignition temp.

723 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

0.8 %, 100 °F
5 %, 150 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.541 (lit.)
n20/D 1.542

bp

207 °C (lit.)

mp

−35 °C (lit.)

density

0.973 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

C1CCc2ccccc2C1

InChI

1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2

InChI key

CXWXQJXEFPUFDZ-UHFFFAOYSA-N

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Related Categories

Application

1,2,3,4-Tetrahydronaphthalene may be used as a solvent in studying the fabrication of solution-processed 6,13-bis(triisopropylsilylethynyl) (TIPS) pentacene thin-film transistors with a cross-linked poly-4-vinylphenol (PVP) dielectric on a polyethersulphone (PES) substrate.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

Signal Word

Danger

Hazard Statements

H304,H315,H319,H351,H411

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2

Supplementary Hazards

EUH019

WGK

WGK 2

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Solution-processed 6, 13-bis (triisopropylsilylethynyl)(TIPS) pentacene thin-film transistors with a polymer dielectric on a flexible substrate.
Shin SI, et al.
Semiconductor Science and Technology, 23(8), 085009-085009 (2008)
Satish Chandra Puri et al.
Journal of biotechnology, 122(4), 494-510 (2005-12-27)
The aryl tetralin lignans are synthesized by Podophyllum sps. and are in great demand worldwide due to their use in synthesis of topoisomerase inhibitors. However, the sustained production of these aryl tetralin lignans requires large-scale harvesting from the natural environments
Michael A Brodney et al.
Bioorganic & medicinal chemistry letters, 21(9), 2637-2640 (2011-01-29)
A novel series of tetralin containing amino imidazoles, derived from modification of the corresponding phenyl acetic acid derivatives is described. Replacement of the amide led to identification of a potent series of tetralin-amino imidazoles with robust central efficacy. The reduction
Laurent Piccolo et al.
ChemSusChem, 5(9), 1717-1723 (2012-09-06)
The development of cleaner fuels from conventional resources requires the finding of new hydrotreatment processes able to improve the combustion performances of fuels and limit undesirable emissions. In the context of gas oil upgrading by selective ring opening, we have
Bin Ma et al.
Bioorganic & medicinal chemistry letters, 20(7), 2264-2269 (2010-03-02)
Modifying FTY720, an immunosuppressant modulator, led to a new series of well phosphorylated tetralin analogs as potent S1P1 receptor agonists. The stereochemistry effect of tetralin ring was probed, and (-)-(R)-2-amino-2-((S)-6-octyl-1,2,3,4-tetrahydronaphthalen-2-yl)propan-1-ol was identified as a good SphK2 substrate and potent S1P1
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