76510
Pentadecane
≥98.0% (GC)
Synonym(s):
n-Pentadecane
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About This Item
Linear Formula:
CH3(CH2)13CH3
CAS Number:
Molecular Weight:
212.41
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-098-1
Beilstein/REAXYS Number:
1698194
MDL number:
Product Name
Pentadecane, ≥98.0% (GC)
InChI key
YCOZIPAWZNQLMR-UHFFFAOYSA-N
InChI
1S/C15H32/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3-15H2,1-2H3
SMILES string
CCCCCCCCCCCCCCC
vapor density
7.4 (vs air)
vapor pressure
1 mmHg ( 91.6 °C)
assay
≥98.0% (GC)
form
liquid
expl. lim.
6.5 %
refractive index
n20/D 1.431 (lit.)
bp
270 °C (lit.)
mp
8-10 °C (lit.)
density
0.769 g/mL at 25 °C (lit.)
Quality Level
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Related Categories
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1
supp_hazards
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Eyeshields, Gloves
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Biosynthesis of phomactins: common intermediate phomactatriene and taxadiene.
Tetsuo Tokiwano et al.
Chemical communications (Cambridge, England), (11)(11), 1324-1325 (2004-05-22)
From 2,2'-methylenedifuran to all stereomeric pentadecane-1,3,5,7,9,11,13,15-octols.
M E Schwenter et al.
The Journal of organic chemistry, 66(23), 7869-7872 (2001-11-10)
Keith D Schwartz et al.
Organic letters, 13(2), 248-251 (2010-12-18)
Conjugate reduction of an enone accompanied by in situ intramolecular aldol condensation was used to construct the tetrasubstituted cyclohexane nucleus of phomactins. Subsequent relay ring-closing metathesis completed the nine-membered ansa bridge of the diterpenoid framework.
Synthesis of homogeneous FePt nanoparticles using a nitrile ligand.
Virginie Monnier et al.
Small (Weinheim an der Bergstrasse, Germany), 4(8), 1139-1142 (2008-07-16)
Heber J Chacon-Madrid et al.
Environmental science & technology, 46(20), 11179-11186 (2012-09-14)
We use a two-dimensional volatility basis set (2D-VBS) box model to simulate secondary organic aerosol (SOA) mass yields of linear oxygenated molecules: n-tridecanal, 2- and 7-tridecanone, 2- and 7-tridecanol, and n-pentadecane. A hybrid model with explicit, a priori treatment of
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