30540
Decane
analytical standard
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About This Item
Linear Formula:
CH3(CH2)8CH3
CAS Number:
Molecular Weight:
142.28
UNSPSC Code:
12352001
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-686-4
Beilstein/REAXYS Number:
1696981
MDL number:
grade
analytical standard
Quality Segment
vapor density
4.9 (vs air)
vapor pressure
1 mmHg ( 16.5 °C), 3.77 mmHg ( 37.7 °C)
assay
≥99.8% (GC)
autoignition temp.
410 °F
shelf life
limited shelf life, expiry date on the label
expl. lim.
2.6 %
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.411 (lit.), n20/D 1.412
bp
174 °C (lit.)
mp
−30 °C (lit.)
density
0.73 g/mL at 25 °C (lit.)
application(s)
petroleum
format
neat
SMILES string
CCCCCCCCCC
InChI
1S/C10H22/c1-3-5-7-9-10-8-6-4-2/h3-10H2,1-2H3
InChI key
DIOQZVSQGTUSAI-UHFFFAOYSA-N
General description
Decane is an alkane hydrocarbon. It exists as a colourless flammable liquid. It is mostly used as solvent. Its vapors may be narcotic at high concentrations.
Application
Decane may have been used as internal standard in GC analysis for determining the product yield during iron-catalyzed cross coupling performed of primary/secondary alkyl halides with aryl Grignard reagent.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
114.8 °F - closed cup
flash_point_c
46.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Iron-catalyzed cross-coupling of primary and secondary alkyl halides with aryl grignard reagents.
Nakamura M
Journal of the American Chemical Society, 126(12), 3686-3687 (2004)
Florent Darriet et al.
Planta medica, 78(4), 386-389 (2012-01-20)
Investigation of the essential oil of the aerial parts of Eryngium maritimum L. from Corsica led to the isolation of one known sesquiterpene (1) and three new oxygenated sesquiterpenes with a muurolane or cadinane skeleton (2-4). Structure assignments of 4
Silke R Kirchner et al.
Journal of biophotonics, 5(1), 40-46 (2011-12-08)
Microfluidic jetting is a promising method to produce giant unilamellar phospholipid vesicles for mimicking living cells in biomedical studies. We have investigated the chemical composition of membranes of vesicles prepared using this approach by means of Raman scattering spectroscopy. The