Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Cambiar Vistas
Acerca de este artículo
Fórmula lineal:
CH3(CH2)12CH3
Número CAS:
Peso molecular:
198.39
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-096-0
Beilstein/REAXYS Number:
1733859
MDL number:
eCl@ss:
39010124
Assay:
≥99.0% (GC)
Form:
liquid
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarlevapor density
6.83 (vs air)
Quality Level
vapor pressure
1 mmHg ( 76.4 °C)
assay
≥99.0% (GC)
form
liquid
autoignition temp.
455 °F
refractive index
n20/D 1.429
bp
252-254 °C (lit.)
mp
5.5 °C (lit.)
density
0.762 g/mL at 20 °C (lit.)
SMILES string
CCCCCCCCCCCCCC
InChI
1S/C14H30/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-14H2,1-2H3
InChI key
BGHCVCJVXZWKCC-UHFFFAOYSA-N
Application
Tetradecane can be used for the synthesis of thermally stable nano-encapsulated phase change materials (NEPCMs), exhibiting thermal energy storage and heat transfer enhancement applications. It can also be used as an n-alkane model for the study of ignition time measurements for larger n-alkanes.
Still not finding the right product?
Explore all of our products under Tetradecane
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1
supp_hazards
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 1
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Preparation and characterization of nano-encapsulated n-tetradecane as phase change material for thermal energy storage
Fang G, et al.
Chemical Engineering Journal, 153(1-3), 217-221 (2009)
A shock tube study of the ignition of n-heptane, n-decane, n-dodecane, and n-tetradecane at elevated pressures
Shen HPS, et al.
Energy and Fuels, 23(5), 2482-2489 (2009)
Vishwakarma Singh et al.
The Journal of organic chemistry, 74(16), 6092-6104 (2009-07-21)
A general and stereoselective methodology for the synthesis of bridged bicyclic octenones having various types of alkenyl chains and a tricyclic framework of secoatisanes and higher analogues is reported. In situ generation and cycloaddition of 2-allyl-6,6-spiroepoxycyclohexadienones with ethyl acrylate gave
