| Name | tetratriacontane |
| Synonyms | ALKANE C34 TETRATRICONTANE TETRATRIACONTANE tetratriacontane N-TETRATRIACONTANE n-Tetratriacontane TETRATRIACONTANE, STANDARD FOR GC |
| CAS | 14167-59-0 |
| EINECS | 238-013-0 |
| InChI | InChI=1/C34H70/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-34H2,1-2H3 |
| Molecular Formula | C34H70 |
| Molar Mass | 478.92 |
| Density | 0.9045 (estimate) |
| Melting Point | 72-75°C(lit.) |
| Boling Point | 285°C2mm Hg(lit.) |
| Flash Point | 345.3°C |
| Solubility | Chloroform |
| Vapor Presure | 5.36E-09mmHg at 25°C |
| Appearance | Flakes |
| Color | White |
| BRN | 1788466 |
| Storage Condition | room temp |
| Refractive Index | 1.4296 |
| MDL | MFCD00009412 |
| WGK Germany | 3 |
| HS Code | 29011000 |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| Application | n-tetradecane is a hydrocarbon derivative that can be used as an organic raw material. |
| Preparation | Synthesis of n-tetralane can be done by coupling method or grafting method, but there are few reports of electrolytic synthesis of n-tetralane. Electrolytic synthesis is an effective organic synthesis method with safe and convenient operation, high efficiency and low energy consumption. |