Name | Decyl Decanoate |
Synonyms | Decyl caprate Decyl Decanoate DECYL DECANOATE capricaciddecylester DECANOIC ACID DECYL ESTER N-CAPRIC ACID N-DECYL ESTER N-CAPRIC ACID N-DECYL ESTER fandachem |
CAS | 1654-86-0 |
EINECS | 216-729-4 |
InChIKey | XAKXZZPEUKNHMA-UHFFFAOYSA-N |
Molecular Formula | C20H40O2 |
Molar Mass | 312.53 |
Density | 0.86 |
Melting Point | 9.7°C |
Boling Point | 159 °C / 2mmHg |
Flash Point | 140 °C |
Storage Condition | 室温,干燥 |
Refractive Index | 1.4410-1.4430 |
MDL | MFCD00059280 |
Application | n-decyl decanoate can be used as an intermediate in organic synthesis and an intermediate in medicine, mainly used in laboratory research and development and chemical pharmaceutical synthesis process. |
preparation | Method 1: N-decyl N-decanoate was prepared as follows: 1mol of N-decanol and 1mol of N-decanoic acid and 0.22 g0.22g2001 (tin oxalate) heating was carried out in a water separator at a temperature of 240 °c for 3 hours. The product was distilled off via a 30cm column (153-168 °c, 0.8 mbar). The product is a colorless, odorless oil. Method 2: 348 parts of capric acid, 383 parts of decyl alcohol, 0.30 parts of stannous oxide catalyst and 1.0 parts of activated carbon were added to the reaction kettle in sequence, and the temperature was gradually raised by stirring under N2, the reaction is maintained at a temperature of 160 to 170 ° C. For 6 hours, and the water generated by the reaction is distilled off. After the heat preservation, it is transferred to the dealcoholization kettle, and the temperature is 160 ° C., vacuum 100Pa for 30 minutes, decanol decanoate was obtained by cooling to 70 ℃ and filtering, and the esterification rate was 99.3%. |
EPA chemical substance information | information is provided by: ofmpeb.epa.gov (external link) |