Name | ethyl undecylenate |
Synonyms | ethyl undecylenate ETHYL UNDECYLENATE ETHYL UNDECYLENOATE RARECHEM AL BI 0169 ETHYL 10-UNDECENOATE HENDECENOIC ACID ETHYL ESTER UNDECYLENIC ACID ETHYL ESTER Undecenoic acid, ethyl ester DELTA 10 CIS UNDECENOIC ACID ETHYL ESTER |
CAS | 692-86-4 |
EINECS | 211-734-8 |
InChI | InChI=1/C13H24O2/c1-3-5-6-7-8-9-10-11-12-13(14)15-4-2/h3H,1,4-12H2,2H3 |
Molecular Formula | C13H24O2 |
Molar Mass | 212.33 |
Density | 0.879 g/mL at 25 °C (lit.) |
Melting Point | -38 °C |
Boling Point | 258-259 °C/761 mmHg (lit.) |
Flash Point | >230°F |
JECFA Number | 343 |
Solubility | Chloroform (Slightly), Methanol (Slightly) |
Vapor Presure | 0.73Pa at 20℃ |
Appearance | Oil |
Color | Clear Yellow |
Storage Condition | Refrigerator |
Refractive Index | n20/D 1.439(lit.) |
MDL | MFCD00009220 |
Physical and Chemical Properties | Colorless to light yellow liquid, with fat aroma, fruit aroma, wax aroma, mould aroma and wine aroma. Boiling point 258~259 deg C, the relative density (d2020)0.8788. Insoluble in water, soluble in ethanol, slightly soluble in propylene glycol. |
WGK Germany | 2 |
RTECS | YQ2978400 |
HS Code | 29161900 |
flammable liquid. The relative density was 0. 8827. Melting Point -38 °c. Boiling point 263.5~265.5 deg C, 131.5 deg C (2.13kPa). Refractive index 4449. Flash point 110 °c. Insoluble in water, soluble in ethanol, ether, acetic acid and other organic solvents.
The raw materials of 11 enoic acid and ethanol were directly esterified under sulfuric acid catalysis to obtain crude ethyl 11 enoate, which was then neutralized, washed with water and fractionated under reduced pressure to obtain a finished product.
It is mainly used as a raw material intermediate for spinal contrast agent sulfophenyl ester.
FEMA | 2461 | ETHYL 10-UNDECENOATE |
LogP | 5.15 |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
toxicity | GRAS(FEMA). |
usage limit | FEMA(mg/kg): Soft drink 1.7; Cold drink 8.7; Candy 10; Baked goods 11; alcohol 5.0. Moderate limits (FDA § 172.515,2000). |
Use | GB 2760-96 specifies the permitted use of flavorants. Mainly used for the preparation of nuts, fruit wine and coconut flavor. It is mainly used as a raw material intermediate of iodophenyl ester as a spinal contrast agent. |
production method | is derived from the esterification of the acid with ethanol. The raw materials of 11 enoic acid and ethanol were directly esterified under sulfuric acid catalysis to obtain crude ethyl 11 enoate, which was then neutralized, washed with water and fractionated under reduced pressure to obtain a finished product. Another method of production is the transesterification of glyceryl triricinoleate with ethanol to obtain ethyl ricinoleate, which is then cleaved at 550-600 °c. The lysate was subjected to fractional distillation under reduced pressure, and a fraction of 150-220 ° C. (2.67-8.0kPa) was collected, which was ethyl 11 enoate. the reaction mixture was obtained by heating to 70 ° C. With ethyl alcohol in the presence of hydrochloric acid followed by esterification and distillation. |