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经验公式(希尔记法):
C10H12
化学文摘社编号:
分子量:
132.20
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-340-2
Beilstein/REAXYS Number:
1446407
MDL number:
InChI key
CXWXQJXEFPUFDZ-UHFFFAOYSA-N
InChI
1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2
SMILES string
C1CCc2ccccc2C1
grade
analytical standard
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
Quality Level
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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
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2
supp_hazards
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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)
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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
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
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
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