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87140

Tetradecane

Name: Tetradecane
Brand: ALDRICH

olefin free, ≥99.0% (GC)

Synonym(s):

n-Tetradecane

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About This Item

Linear Formula:

CH₃(CH₂)₁₂CH₃

CAS Number:

629-59-4

Molecular Weight:

198.39

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

57653230

EC Number:

211-096-0

Beilstein/REAXYS Number:

1733859

MDL number:

MFCD00008986

eCl@ss:

39010124

Assay:

≥99.0% (GC)

Form:

liquid

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Properties

vapor density

6.83 (vs air)

Quality Level

100

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

Description

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.

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pictograms

GHS08

signalword

Danger

hcodes

H304

pcodes

P301 + P310 - P331 - P405 - P501

Hazard Classifications

Asp. Tox. 1

supp_hazards

EUH066

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves

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Protocols

US EPA Method 8015 (modified): GC Analysis of Diesel Range Organics (DRO) on SLB®-5ms (20 m x 0.18 mm I.D., 0.18 µm), Fast GC Analysis

Separation of Decane; Dodecane; Tetradecane; Hexadecane; Octadecane; Eicosane; Docosane; Tetracosane; Hexacosane; Octacosane

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)

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)

Diels-Alder cycloaddition and ring-closing metathesis: a versatile, stereoselective, and general route to embellished bridged bicyclic systems, carbocyclic framework of secoatisanes, and homologues.

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

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Global Trade Item Number

SKU	GTIN
87140-50ML	04061833049938
87140-250ML	04061833049921