Name | Ethyl 3-aminobenzoate |
Synonyms | AKOS BB-7960 Ethyl 3-aminobenzoate m-Ethoxycarbonylaniline Benzocaine EP Impurity C 3-amino-benzoicaciethylester 3-AMINOBENZOIC ACID ETHYL ESTER 3-Aminobenzoic acid ethyl ester m-Aminobenzoic acid, ethyl ester Benzoic acid, m-amino-, ethyl ester 3-(ethoxycarbonyl)anilinium methanesulfonate BENZOCAINE IMPURITY C (ETHYL 3-AMINOBENZOATE) Ethyl 3-aminobenzoate,(3-Aminobenzoic acid ethyl ester) |
CAS | 582-33-2 |
EINECS | 209-482-9 |
InChI | InChI=1/C9H11NO2.ClH/c1-2-12-9(11)7-4-3-5-8(10)6-7;/h3-6H,2,10H2,1H3;1H |
InChIKey | ZMCBYSBVJIMENC-UHFFFAOYSA-N |
Molecular Formula | C9H11NO2 |
Molar Mass | 165.19 |
Density | 1.107 g/mL at 25 °C (lit.) |
Melting Point | 27-30°C |
Boling Point | 172-175 °C/13 mmHg (lit.) |
Specific Rotation(α) | n20/D 1·560(lit·) |
Flash Point | >230°F |
Vapor Presure | 0.0016mmHg at 25°C |
Appearance | oily liquid |
Specific Gravity | 1.127 (20/4℃) |
Color | Clear yellow to light brown |
BRN | 1101967 |
pKa | 3.50±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | n20/D 1.560(lit.) |
MDL | MFCD00007794 |
Physical and Chemical Properties | Oily liquid. Boiling point 294 ℃, 1.73-175 ℃ (144 kPa), 0.67 ℃ (1.1248 kPa), relative density 1.5600 (22/4 ℃), refractive index (22 ℃). Soluble in alcohol and ether, slightly soluble in water. |
Use | Used as an intermediate in organic synthesis |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29224999 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | for organic synthesis. Ethyl M-aminobenzoate mesylate (Tricaine[886-86-2]) is a fish anesthetic. used as intermediate in organic synthesis |
production method | is obtained by esterification of M-aminobenzoic acid with ethanol in the presence of hydrochloric acid. Anhydrous ethanol was cooled while keeping it below 10 °c, hydrochloric acid was passed to saturation, and dried m-aminobenzoic acid was added. Then heated to reflux for 24h. After recovering the ethanol, it is poured into ice water, neutralized to pH 8 with sodium carbonate, and then washed with water to obtain a crude product. |