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1,2,3,4-Tetrahydronaphthalin

analytical standard

Synonym(e):

Tetralin Lösungsmittel

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About This Item

Empirische Formel (Hill-System):
C10H12
CAS-Nummer:
119-64-2
Molekulargewicht:
132.20
Beilstein:
1446407
EG-Nummer:
204-340-2
MDL-Nummer:
MFCD00001733
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329770463
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Dampfdichte

4.55 (vs air)

Dampfdruck

0.18 mmHg ( 20 °C)

Assay

≥99.5% (GC)

Selbstzündungstemp.

723 °F

Haltbarkeit

limited shelf life, expiry date on the label

Expl.-Gr.

0.8 %, 100 °F
5 %, 150 °F

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

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

bp

207 °C (lit.)

mp (Schmelzpunkt)

−35 °C (lit.)

Dichte

0.973 g/mL at 25 °C (lit.)

Anwendung(en)

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

InChIKey

CXWXQJXEFPUFDZ-UHFFFAOYSA-N

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Anwendung

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.

Rechtliche Hinweise

Signalwort

Danger

Gefahreneinstufungen

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

Zusätzliche Gefahrenhinweise

EUH019

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

159.8 °F - closed cup

Flammpunkt (°C)

71 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Analysenzertifikate (COA)

Lot/Batch Number
BCCL9360
BCCG1981
BCCB0505
BCCB4389
BCBS0492V

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04070

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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
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
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
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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