P3406
十五烷
≥99%
别名:
n -十五烷
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关于此项目
线性分子式:
CH3(CH2)13CH3
化学文摘社编号:
分子量:
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
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.)
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Application
十五烷是一种高潜热 (~168 kJ/kg)、低熔点的直链烷烃。这些属性使其成为冷却应用的相更改材料 (PCM) 的理想候选材料。
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1
supp_hazards
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Eyeshields, Gloves
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)
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)
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.
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
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