102415
1,2,3,4-Tetrahydronaphthalene
reagent grade, ≥97%
Synonym(s):
Tetralin solvent
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C10H12
CAS Number:
Molecular Weight:
132.20
EC Number:
204-340-2
UNSPSC Code:
12352002
PubChem Substance ID:
Beilstein/REAXYS Number:
1446407
MDL number:
grade
reagent grade
vapor density
4.55 (vs air)
vapor pressure
0.18 mmHg ( 20 °C)
assay
≥97%
autoignition temp.
723 °F
expl. lim.
0.8 %, 100 °F, 5 %, 150 °F
refractive index
n20/D 1.541 (lit.)
bp
207 °C (lit.)
mp
−35 °C (lit.)
density
0.973 g/mL at 25 °C (lit.)
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
Legal Information
Still not finding the right product?
Explore all of our products under 1,2,3,4-Tetrahydronaphthalene
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2
supp_hazards
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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