P3406
Pentadecane
≥99%
Synonym(s):
n-Pentadecane
Sign In to View Organizational & Contract Pricing.
Select a Size
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:
Assay:
≥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 %
Quality Level
bp
270 °C (lit.)
mp
8-10 °C (lit.)
density
0.769 g/mL at 25 °C (lit.)
Looking for similar products? Visit Product Comparison Guide
Related Categories
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
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.
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)
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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service