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P3406

Sigma-Aldrich

Pentadecane

≥99%

Synonym(s):

n-Pentadecane

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About This Item

Linear Formula:
CH3(CH2)13CH3
CAS Number:
629-62-9
Molecular Weight:
212.41
Beilstein/REAXYS Number:
1698194
EC Number:
211-098-1
MDL number:
MFCD00008990
UNSPSC Code:
12352100
PubChem Substance ID:
24898408
NACRES:
NA.22

vapor density

7.4 (vs air)

Quality Level

100

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.)

SMILES string

CCCCCCCCCCCCCCC

InChI

1S/C15H32/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3-15H2,1-2H3

InChI key

YCOZIPAWZNQLMR-UHFFFAOYSA-N

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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.

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H304

Hazard Classifications

Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

219.2 °F - closed cup

flash_point_c

104 °C - closed cup

ppe

Eyeshields, Gloves

Certificates of Analysis (COA)

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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)
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
Kevin M Foote et al.
Organic & biomolecular chemistry, 1(22), 3917-3948 (2003-12-11)
A concise synthesis of the tricyclic furanochroman unit 3 found in the PAF antagonist phomactin A (1) isolated from the marine fungus Phoma sp., is described. In complementary studies, a variety of synthetic routes towards the bicyclo[9.3.1]pentadecane ring system 4
Thembelani E Nomkoko et al.
Dalton transactions (Cambridge, England : 2003), (33)(33), 4029-4038 (2006-10-10)
The equilibrium constants of Cu(II), Zn(II), Ca(II) and Gd(III) with 1,15-bis(N,N-dimethyl)-5,11-dioxo-8-(N-benzyl)-1,4,8,12,15-pentaazapentadecane (La) have been studied at 25 degrees C and an ionic strength of 0.15 mol dm-3. Copper forms more stable complexes with La than the other metal ions investigated.
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