N-DOCOSANE

N-DOCOSANE Basic information
Product Name:N-DOCOSANE
Synonyms:n-Docosane, δ13C: -30.35;Docosane [Standard Material for GC];n-Docosane 1g [629-97-0];Docosane ;n-Docosane, 99% 100GR;Twenty-two alkyl;Docosane 99%;n-Docosane 0.5
CAS:629-97-0
MF:C22H46
MW:310.6
EINECS:211-121-5
Product Categories:Aloe Vera;Building Blocks;Chemical Synthesis;Nutrition Research;Organic Building Blocks;Phytochemicals by Plant (Food/Spice/Herb);Plantago ovata;Alkanes;Organic Building Blocks;Alphabetic;DJ - DZChemical Class;Hydrocarbons;Neats;DJ - DZ;Alpha Sort;D;DAlphabetic;Volatiles/ Semivolatiles;Miscellaneous Natural Products;Analytical Chemistry;n-Paraffins (GC Standard);Standard Materials for GC;Acyclic
Mol File:629-97-0.mol
N-DOCOSANE Structure
N-DOCOSANE Chemical Properties
Melting point 42-45 °C(lit.)
Boiling point 369 °C(lit.)
density 0.778 g/mL at 25 °C(lit.)
vapor density 10.8 (vs air)
vapor pressure <1 mm Hg ( 21.1 °C)
refractive index 1.4455
Fp >230 °F
storage temp. room temp
solubility soluble in Benzene,Toluene
form Crystalline Solid
Specific Gravity0.778
color White
Odorat 100.00?%. waxy
Water Solubility Insoluble in water. Soluble in alcohol.
BRN 1702206
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKeyHOWGUJZVBDQJKV-UHFFFAOYSA-N
LogP11.47 at 25℃
CAS DataBase Reference629-97-0(CAS DataBase Reference)
EPA Substance Registry SystemDocosane (629-97-0)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
TSCA Yes
HS Code 29011000
Hazardous Substances Data629-97-0(Hazardous Substances Data)
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
N-DOCOSANE Usage And Synthesis
Chemical Propertiescolourless crystalline solid
UsesIt is employed as a perfuming agent in cosmetics industry. It is also used in organic synthesis, calibration, and temperature sensing equipment. Docosane is used to investigate commercially available waxes in the form of thin disc samples as possible diffraction intensity standards for macromolecular crystallography synchrotron beamlines.
DefinitionChEBI: Docosane is a straight-chain alkane with 22 carbon atoms. It has a role as a plant metabolite.
General DescriptionSolid. Insoluble in water. Used in organic synthesis, calibration, and temperature sensing equipment.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileSaturated aliphatic hydrocarbons, such as N-DOCOSANE, 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.
Purification MethodsCrystallise docosane from EtOH or ether. [Beilstein 1 IV 572.]
N-DOCOSANE Preparation Products And Raw materials
7,16-Diphenyl-1,5,10,14-tetraazatricyclo[14.2.2.27,10]docosane,7,16-Diphenyl-1,5,10,14-tetraazatricyclo[14.2.2.27,10]docosane OCTACOSANOIC ACID Sodium cholate docosane,2-methyl 3',4'-(DIDODECYLOXY)BENZALDEHYDE 6-KETOCHOLESTANOL 1-HEXACOSANOL Tetracosanedioic acid Docosane-1-amine,Docosane-1-amine APOCHOLIC ACID Aluminum tris(docosane-1-olate),Aluminum tris(docosane-1-olate) 21,22-Dimethoxytricyclo[15.3.1.17,11]docosane,21,22-Dimethoxytricyclo[15.3.1.17,11]docosane 3-(3-Methoxy-4-hydroxyphenyl)propenoic acid docosane-1-yl ester,3-(3-Methoxy-4-hydroxyphenyl)propenoic acid docosane-1-yl ester Tetracyclo[14.3.1.14,8.19,13]docosane-1(20),4(22),5,7,9,11,13(21),16,18-nonaene,Tetracyclo[14.3.1.14,8.19,13]docosane-1(20),4(22),5,7,9,11,13(21),16,18-nonaene BEHENIC ACID METHYL ESTER 5,14-Dimethyl-7,16-diphenyl-1,5,10,14-tetraazatricyclo[14.2.2.27,10]docosane,5,14-Dimethyl-7,16-diphenyl-1,5,10,14-tetraazatricyclo[14.2.2.27,10]docosane Taurodeoxycholic acid sodium salt Cholesteryl behenate

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