ChemicalBook > Product Catalog >Organic Chemistry >Hydrocarbons and derivatives >Acyclic hydrocarbons >Heneicosane

Heneicosane

Heneicosane Suppliers list
Company Name: SEDIN Pionerr Technology & Industry Development limited  Gold
Tel: 0351-12179486 13233602527
Email: 1211028710@qq.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: future industrial shanghai co., ltd  
Tel: 400-0066400 13621662912
Email: sales@jonln.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com

Heneicosane manufacturers

  • N-HENEICOSANE
  • N-HENEICOSANE pictures
  • $100.00
  • 2026-09-02
  • CAS:629-94-7
  • Min. Order: 1KG
  • Purity: 99%
  • Heneicosane
  • Heneicosane pictures
  • $29.00
  • 2026-05-11
  • CAS:629-94-7
  • Purity: 98.69%
  • Supply Ability: 10g
  • N-HENEICOSANE
  • N-HENEICOSANE pictures
  • 2026-04-13
  • CAS:629-94-7
  • Min. Order: 1ton
  • Purity: 78%
  • Supply Ability: 200
Heneicosane Basic information
Product Name:Heneicosane
Synonyms:Heneicosane 98%;n-Heneicosane [Standard Material];N-ENEICOSANE;HENEICOSANE, STANDARD FOR GC;N-HENEICOSANE 99+%;Jenicosane.;uneicosane;n-Heneicosane,98%
CAS:629-94-7
MF:C21H44
MW:296.57
EINECS:211-118-9
Product Categories:Analytical Chemistry;n-Paraffins (GC Standard);Standard Materials for GC;Acyclic;Alkanes;Organic Building Blocks;Alphabetic;H;HA -HTChemical Class;Hydrocarbons;Neats;Aliphatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:629-94-7.mol
Heneicosane Structure
Heneicosane Chemical Properties
Melting point 39-41 °C(lit.)
Boiling point 100 °C2 mm Hg(lit.)
density 0,792 g/cm3
vapor density 10.3 (vs air)
vapor pressure <1 mm Hg ( 20 °C)
refractive index 1.4352 (589.3 nm 45℃)
Fp >230 °F
storage temp. Refrigerator
solubility Chloroform, Hexane
form Crystalline Chunks, Crystals, or Flakes
color White
Odorat 100.00%. waxy
BRN 1748500
Henry's Law Constant7.3×10-8 mol/(m3Pa) at 25℃, Hilal et al. (2008)
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
Major Applicationpetroleum
Cosmetics Ingredients FunctionsPERFUMING
InChI1S/C21H44/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h3-21H2,1-2H3
InChIKeyFNAZRRHPUDJQCJ-UHFFFAOYSA-N
SMILESCCCCCCCCCCCCCCCCCCCCC
LogP11.406 (est)
CAS DataBase Reference629-94-7(CAS DataBase Reference)
EPA Substance Registry SystemHeneicosane (629-94-7)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
RTECS 211-118-9
TSCA TSCA listed
HS Code 29011000
Storage Class11 - Combustible Solids
Hazardous Substances Data629-94-7(Hazardous Substances Data)
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Heneicosane Usage And Synthesis
DescriptionHeneicosane (also known as n-Heneicosane) is a potential organic phase-change material (PCM) used for thermal energy storage[1]. In its pure form, it has a melting point of 313.55 K (approximately 40.4 °C) and offers advantages such as good stability, low supercooling and low cost. However, due to its relatively low thermal conductivity, it is often combined with highly thermally conductive fillers (such as graphene) to form composite materials, which are used in solar thermal energy storage, passive cooling of electronic devices, and waste heat recovery systems.
Chemical Propertieswhite waxy solid
UsesHeneicosane is a long chain saturated aliphatic hydrocarbon found in coal tars and fossil organic matter. Heneicosane has a high flashpoint which makes it an inefficient fuel for use in the petrochemical industry. Heneicosane is usually present in the form of paraffin wax.
DefinitionChEBI: An alkane that has 21 carbons and a straight-chain structure. It has been isolated from plants like Periploca laevigata and Carthamus tinctorius.
Synthesis Reference(s)Tetrahedron Letters, 17, p. 2643, 1976 DOI: 10.1016/S0040-4039(00)91757-X
General DescriptionCrystals.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileSaturated aliphatic hydrocarbons, such as N-HENEICOSANE, 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.
Synthesis

Preparation method for one-time preparation of n-hexadecane in the following steps:

(1). Mix 1510.5 g (10 mol) of n-pentyl bromide and 3053.5 g (10 mol) of n-hexadecyl bromide to form a bromoalkane mixture, and set aside;

(2). Weigh 483 g (21 mol) of metallic sodium and cut it into small thin strips with an area of about 1 x 3 cm2, and set aside;

(3). In the reaction kettle put 50g of bromoalkane mixture as well as 20g of sodium metal, stirring to raise the temperature to 80 , relying on the reaction heating, and maintain the reaction temperature of 120 , and constantly dropwise addition of the remaining bromoalkane mixture, and add the sodium metal, maintain the micro reflux state, the addition is completed, control the temperature at 140 , constant temperature for 2 hours;

(4). Sequentially add 400 g of 95% ethanol as well as 1000 ml of water, split the organic matter, washed with water to neutral, dried with anhydrous magnesium sulfate, distilled to collect 260 ~ 280 fractions, the fraction plus 600 g of concentrated potassium sulfate washed to the acid layer light yellow, washed with water the organic phase to neutral, drying, through the fractional distillation column to collect 500 g of 96% of the n-decane, 600 g of 98% of the n-xyloxanes, the resulting n-alkane content of 96% to 98%.

Said n-pentane and n-hexadecyl bromide molar ratio is 1:1, the reactor is a three-ported flask consisting of a stirrer, a separatory funnel and a reflux condenser, said strong oxidizing agent is concentrated sulfuric acid or acidic potassium permanganate.

References[1] Sinaga, R. (2026). Thermal Performance Enhancement of Heneicosane as Thermal Energy Storage Material: A Molecular Dynamic Study. Energy Storage, 8 1. https://doi.org/10.1002/est2.70334
Heneicosane Preparation Products And Raw materials
Tag:Heneicosane(629-94-7) Related Product Information
N-HEPTACOSANE N-HEXACOSANE n-Octacosane N-NONACOSANE Docosane Lignoceric acid N-HENEICOSANE-D44,N-HENEICOSANE-D44 N-TETRACOSANE-D50 N-EICOSANE-D42 N-HEPTANE-D16 N-HEXYLAMINE HYDROCHLORIDE PROPYLCYCLOHEXANE Azetidine Tricosane N-Tetracosane N-Tetratriacontane N-Pentacosane Heneicosanol