| Weight | 324.637 g/mol |
|---|---|
| Formula | C23H48 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 20 |
TRICOSANE (638-67-5)
n-tricosane
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- Disorder in the pseudohexagonal rotator phase of n-alkanes: molecular-dynamics calculations for tricosane (Molecular Physics, 1989)
- Studies on alkane biosynthesis in epidermis of Allium porrum L. leaves: Direct synthesis of tricosane from lignoceric acid (Archives of Biochemistry and Biophysics, 1974)
- Phase Diagram of n-Tricosane and n-Pentacosane Mixtures (Molecular Crystals and Liquid Crystals, 1996)
- Decarboxylation of tetracosanoic acid to n-Tricosane in the termite Zootermopsis angusticollis (Comparative Biochemistry and Physiology B, 1980)
- Diagram of the n-tricosane-n-tetracosane mixtures: Corrections (Thermochimica Acta, 1997)
- Phase diagram of n-heneicosane and n-tricosane molecular alloys (Journal of Molecular Structure, 1996)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - n-tricosane
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SMILESCCCCCCCCCCCCCCCCCCCCCCC
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InChIKeyFIGVVZUWCLSUEI-UHFFFAOYSA-N
- Pubchem - TRICOSANE
- Wikipedia - Tricosane
Higher alkanes are alkanes having nine or more carbon atoms. Nonane is the lightest alkane to have a flash point above 25C, and is not classified as dangerously flammable. The term higher alkanes is sometimes used literally as "alkanes with a higher number of carbon atoms".
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