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95462

Supelco

1,2,3,4-Tetrahydronaphthalene

analytical standard

Sinonimo/i:

Tetralin solvent

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About This Item

Formula empirica (notazione di Hill):
C10H12
Numero CAS:
119-64-2
Peso molecolare:
132.20
Beilstein:
1446407
Numero CE:
204-340-2
Numero MDL:
MFCD00001733
Codice UNSPSC:
41116107
ID PubChem:
329770463
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Densità del vapore

4.55 (vs air)

Tensione di vapore

0.18 mmHg ( 20 °C)

Saggio

≥99.5% (GC)

Temp. autoaccensione

723 °F

Durata

limited shelf life, expiry date on the label

Limite di esplosione

0.8 %, 100 °F
5 %, 150 °F

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

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

P. eboll.

207 °C (lit.)

Punto di fusione

−35 °C (lit.)

Densità

0.973 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Stringa SMILE

C1CCc2ccccc2C1

InChI

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

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Applicazioni

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.

Note legali

Avvertenze

Danger

Indicazioni di pericolo

H304,H315,H319,H351,H411

Classi di pericolo

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

Rischi supp

EUH019

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

159.8 °F - closed cup

Punto d’infiammabilità (°C)

71 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL9360
BCCG1981
BCCB0505
BCCB4389
BCBS0492V

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Supelco

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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)
Laura Ledesma García et al.
The Journal of biological chemistry, 286(3), 1709-1718 (2010-11-12)
Previous genetic studies in Sphingomonas macrogolitabida strain TFA have established that expression of genes involved in tetralin biodegradation (thn genes) requires the function of the LysR type activator ThnR and also ThnY. Sequence comparison indicated that ThnY is homologous to
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
Laura Tomás-Gallardo et al.
Microbial biotechnology, 2(2), 262-273 (2009-03-01)
The tetralin biodegradation pathway in Rhodococcus sp. strain TFB, a Gram-positive bacterium resistant to genetic manipulation, was characterized using a proteomic approach. Relative protein expression in cell free extracts from tetralin- and glucose-grown cells was compared using the 2D-DIGE technique.
Laura Tomás-Gallardo et al.
Applied and environmental microbiology, 78(15), 5460-5462 (2012-05-29)
Glucose catabolite repression of tetralin catabolic genes in Rhodococcus sp. strain TFB was shown to be exerted by a protein homologous to transcriptional regulators of the cyclic AMP receptor (CRP)-FNR family. The protein was detected bound to putative CRP-like boxes
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