P3406
Pentadecane
≥99%
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, ≥99%
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
≥99%
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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Application
Pentadecane is a linear alkane with high latent heat (~168 kJ/kg) and low melting point. These properties make it an ideal candidate as a phase change material (PCM) for cooling applications.
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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Thermal properties of n-pentadecane, n-heptadecane and n-nonadecane in the solid/liquid phase change region.
Velez C, et al.
International Journal of Thermal Sciences, 94, 139-146 (2015)
The thermodynamic properties of n-pentadecane in the liquid state, determined by the results of measurements of sound velocity.
Dovnar D, et al.
High Temperature, 39(6), 835-839 (2001)
The capric?lauric acid and pentadecane combination as phase change material for cooling applications
Dimaano.RNM and Watanabe T
Applied Thermal Engineering, 22(4), 365-377 (2002)
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.
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)
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