Acetic acid, ethoxy-, ethyl ester
Ethyl ethoxyacetate
CAS: 817-95-8
Molecular Formula: C6H12O3
Acetic acid, ethoxy-, ethyl ester - Names and Identifiers
| Name | Ethyl ethoxyacetate |
| Synonyms | DIETHYL GLYCOLATE TIMTEC-BB SBB007971 ETHYL ETHOXYACETATE Ethyl ethoxyacetate 2-ETHYL ETHOXYACETATE ETHYL 2-ETHOXYACETATE ETHOXYACETIC ACID-ETHYL ESTER 2-ETHOXYACETIC ACID ETHYL ESTER Acetic acid, ethoxy-, ethyl ester |
| CAS | 817-95-8 |
| EINECS | 212-447-0 |
| InChI | InChI=1/C6H12O3/c1-3-8-5-6(7)9-4-2/h3-5H2,1-2H3 |
Acetic acid, ethoxy-, ethyl ester - Physico-chemical Properties
| Molecular Formula | C6H12O3 |
| Molar Mass | 132.16 |
| Density | 0.975g/mLat 25°C(lit.) |
| Boling Point | 156°C(lit.) |
| Flash Point | 119°F |
| Water Solubility | insoluble |
| Vapor Presure | 2.68mmHg at 25°C |
| Appearance | Liquid |
| Color | Clear colorless |
| BRN | 1749545 |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | n20/D 1.402(lit.) |
| Physical and Chemical Properties | Colorless liquid. Boiling point of 0.970-156 deg C, the relative density of 1.403 deg C (20/4 deg C), refractive index of (20 deg C). Soluble in ethanol, ether, insoluble in water. |
| Use | Used as organic solvents, pharmaceutical, pesticide intermediates |
Acetic acid, ethoxy-, ethyl ester - Risk and Safety
| Risk Codes | 10 - Flammable |
| Safety Description | 16 - Keep away from sources of ignition. |
| UN IDs | UN 3272 3/PG 3 |
| WGK Germany | 3 |
| HS Code | 29189900 |
| Hazard Class | 3.2 |
| Packing Group | III |
Acetic acid, ethoxy-, ethyl ester - Reference Information
| NIST chemical information | information provided by: webbook.nist.gov (external link) |
| EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
| Introduction | ethyl 2-ethoxyacetate is colorless liquid, soluble in ethanol, ether, insoluble in water. It can be used as an intermediate in organic synthesis. |
| Use | for intermediates in organic synthesis. used as organic solvent, pharmaceutical, pesticide intermediates |
| production method | dry hydrogen chloride gas was introduced into a mixture of ethoxyacetic acid and absolute ethanol, and the mixture was cooled to saturation, the reaction was allowed to stand for 24h at room temperature, and saturated sodium carbonate solution was carefully added until the reaction solution was alkaline to litmus. It was extracted with diethyl ether, and the extract was distilled off under atmospheric pressure. The normal boiling fraction was collected to obtain ethyl ethoxylate in the yield of 69%-72%, |
Last Update：2024-04-09 02:00:12
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View History
Acetic acid, ethoxy-, ethyl ester
复合烷基吡啶 吡啶碱
Mupirocin Calcium EP Impurity E
2-(5-(4-(4,5-二氢-1H-咪唑-2-基)苯基)呋喃-2-基)-1H-苯并[d]咪唑 二盐酸盐
353249-09-9
利奈唑胺相关化合物B(USP)
4(3H)-Pteridinone, 6-(4-iodophenyl)-
1-(2-氯吡啶-3-羰基)哌嗪盐酸盐
2-溴-5H-吡咯并[2,3-b]吡嗪-7-羧酸
PROCYSTEINE ETHYL ESTER (L-OXOTHIAZOLIDINE-4-CARB
复合烷基吡啶 吡啶碱
Mupirocin Calcium EP Impurity E
2-(5-(4-(4,5-二氢-1H-咪唑-2-基)苯基)呋喃-2-基)-1H-苯并[d]咪唑 二盐酸盐
353249-09-9
利奈唑胺相关化合物B(USP)
4(3H)-Pteridinone, 6-(4-iodophenyl)-
1-(2-氯吡啶-3-羰基)哌嗪盐酸盐
2-溴-5H-吡咯并[2,3-b]吡嗪-7-羧酸
PROCYSTEINE ETHYL ESTER (L-OXOTHIAZOLIDINE-4-CARB