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n-Octacosane

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n-Octacosane Basic information

Product Name:
n-Octacosane
Synonyms:
  • ALKANE C28
  • N-OCTACOSANE, 1000MG, NEAT
  • OCTACOSANE, STANDARD FOR GC
  • n-octocosane
  • N-OCTACOSANE
  • OCTACOSANE
  • Octacosane, 99+%
  • n-Octcosane
CAS:
630-02-4
MF:
C28H58
MW:
394.76
EINECS:
211-125-7
Product Categories:
  • Alphabetic
  • Chemical Class
  • Hydrocarbons
  • NeatsAnalytical Standards
  • O
  • Alpha Sort
  • N-OAnalytical Standards
  • Volatiles/ Semivolatiles
  • Acyclic
  • Alkanes
  • Organic Building Blocks
Mol File:
630-02-4.mol
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n-Octacosane Chemical Properties

Melting point:
57-62 °C(lit.)
Boiling point:
278 °C15 mm Hg(lit.)
Density 
0.8067
vapor density 
13.6 (vs air)
vapor pressure 
<1 mm Hg ( 20 °C)
refractive index 
1.4330
Flash point:
227 °C
storage temp. 
room temp
form 
Shiny Flakes or Powder
color 
White
Water Solubility 
Soluble in chloroform, acetone, benzene, and toluene. Insoluble in water.
BRN 
1770570
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
Major Application
petroleum
InChI
1S/C28H58/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-28H2,1-2H3
InChIKey
ZYURHZPYMFLWSH-UHFFFAOYSA-N
SMILES
CCCCCCCCCCCCCCCCCCCCCCCCCCCC
LogP
14.973 (est)
CAS DataBase Reference
630-02-4(CAS DataBase Reference)
NIST Chemistry Reference
Octacosane(630-02-4)
EPA Substance Registry System
Octacosane (630-02-4)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
TSCA 
TSCA listed
HS Code 
29011090
Storage Class
11 - Combustible Solids
Hazardous Substances Data
630-02-4(Hazardous Substances Data)

MSDS

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n-Octacosane Usage And Synthesis

Chemical Properties

white powder or waxy solid

Uses

Refer to the productμs Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Definition

ChEBI: A straight-chain alkane containing 28 carbon atoms.

General Description

Waxy hydrocarbon, insoluble in water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Saturated aliphatic hydrocarbons, such as n-Octacosane, may be incompatible with strong oxidizing agents like nitric acid. Charring of the hydrocarbon may occur followed by ignition of unreacted hydrocarbon and other nearby combustibles. In other settings, aliphatic saturated hydrocarbons are mostly unreactive. They are not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, they burn exothermically to produce carbon dioxide and water.

Fire Hazard

Flash point data for n-Octacosane is not available, but n-Octacosane is probably combustible.

Synthesis

A method of preparing n-octacosane in the steps of:

(1) take 2773 g (10 mol) of brominated n-tetradecane and set aside;

(2) Weigh 241.5 g (10.5 mol) of sodium metal and cut it into small thin strips measuring about 1×3 cm2, set aside;

(3) in the reaction kettle put 50g bromine n-tetradecane as well as 20g sodium metal, stirring to warm up to 80 ??, withdraw the heat source, relying on the reaction heating, and maintained at 120 ??, constantly adding the remaining bromine n-tetradecane dropwise, and add sodium metal, to maintain a slight reflux state, the addition of the material is completed, the control of the temperature of 160 ??, the constant temperature for 2 hours;

(4) sequentially add 400 g of 95% ethanol reaction after adding 1000 ml of water, divided into organic matter, water washing to neutral, dried with anhydrous magnesium sulfate, distillation to collect 140 ?? / 1 mmHg before the fraction, the remaining fraction washed with concentrated sulfuric acid to light yellow, washed with water to neutral, drying the proceeds of benzene with repeated purification three times, drained, to obtain the white crystalline eicosanoctadecane as 1.38 Kg, mp60-62 ??. Said brominated n-tetradecane of sodium metal molar ratio of 1:1.01.

Purification Methods

Purify it by forming its adduct with urea, washing it and crystallising it from acetone/water. [McCubbin Trans Faraday Soc 58 2307 1962.] Crystallise it then from hot filtered isopropyl ether solution (10mL/g). [Beilstein 1 IV 588.]

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