N-TRICOSANE
N-TRICOSANE Basic information
- Product Name:
- N-TRICOSANE
- Synonyms:
-
- n-Tricosane,99%
- N-TRICOSANOIC
- n-Tricosane [Standard Material]
- Tricosane [Standard Material]
- n-Tricosane, δ13C: -26.71
- Tricosane [Standard Material for GC]
- n-Tricosane ,98%
- Tricosane
- CAS:
- 638-67-5
- MF:
- C23H48
- MW:
- 324.63
- EINECS:
- 211-347-4
- Product Categories:
-
- Analytical Chemistry
- n-Paraffins (GC Standard)
- Standard Materials for GC
- Acyclic
- Alkanes
- Organic Building Blocks
- Chemical Class
- Hydrocarbons
- NeatsAlphabetic
- TP - TZ
- Mol File:
- 638-67-5.mol
N-TRICOSANE Chemical Properties
- Melting point:
- 46-47 °C(lit.)
- Boiling point:
- 199-200 °C3 mm Hg(lit.)
- Density
- 0,7969 g/cm3
- refractive index
- 1.4468
- Flash point:
- >230 °F
- storage temp.
- Store below +30°C.
- solubility
- dioxane: 0.1 g/mL, clear, colorless
- form
- Shiny Flakes
- color
- White
- Odor
- at 100.00?%. waxy
- Water Solubility
- Insoluble in water.
- BRN
- 1756000
- Stability:
- Stable. Incompatible with strong oxidizing agents.
- LogP
- 12.425 (est)
- CAS DataBase Reference
- 638-67-5(CAS DataBase Reference)
- EPA Substance Registry System
- Tricosane (638-67-5)
Safety Information
- Risk Statements
- 36/37/38
- Safety Statements
- 22-24/25-26
- WGK Germany
- 3
- RTECS
- 211-347-4
- TSCA
- Yes
- HS Code
- 29011000
- Hazardous Substances Data
- 638-67-5(Hazardous Substances Data)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
N-TRICOSANE Usage And Synthesis
Chemical Properties
white flakes
Uses
Organic synthesis.
Uses
n-Tricosane is used as a pharmaceutical intermediate.
Definition
ChEBI: A straight chain alkane containing 23 carbon atoms.
General Description
Leafs (ether-alcohol).
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Saturated aliphatic hydrocarbons, such as N-TRICOSANE, 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.
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