4-Amino-3-ethylbenzoic acid
- Product Name
- 4-Amino-3-ethylbenzoic acid
- CAS No.
- 51688-75-6
- Chemical Name
- 4-Amino-3-ethylbenzoic acid
- Synonyms
- 4-Amino-3-ethylbenzoicaci;Benzoic acid, 4-amino-3-ethyl-;4-Amino-3-ethylbenzoic acid hydrochloride
- CBNumber
- CB7967456
- Molecular Formula
- C9H11NO2
- Formula Weight
- 165.19
- MOL File
- 51688-75-6.mol
4-Amino-3-ethylbenzoic acid Property
- Melting point:
- 152-154 °C(Solv: water (7732-18-5); ethanol (64-17-5))
- Boiling point:
- 348.3±35.0 °C(Predicted)
- Density
- 1.205±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 4.93±0.10(Predicted)
- Appearance
- Brown to reddish brown Solid
Safety
- HS Code
- 2935009090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H317May cause an allergic skin reaction
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- CHM0095114
- Product name
- 4-AMINO-3-ETHYL-BENZOIC ACID
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $500.7
- Updated
- 2021/12/16
- Product number
- 51688756
- Product name
- 4-Amino-3-ethylbenzoicacid
- Packaging
- 500mg
- Price
- $790.55
- Updated
- 2021/12/16
- Product number
- CD12066063
- Product name
- 4-Amino-3-ethylbenzoicacid
- Purity
- 98%
- Packaging
- 5g
- Price
- $234
- Updated
- 2021/12/16
- Product number
- CD12066063
- Product name
- 4-Amino-3-ethylbenzoicacid
- Purity
- 98%
- Packaging
- 10g
- Price
- $455
- Updated
- 2021/12/16
4-Amino-3-ethylbenzoic acid Chemical Properties,Usage,Production
Synthesis
34921-76-1
51688-75-6
Preparation of 4-amino-3-ethylbenzoic acid: N1-(4-cyano-2-ethylphenyl)acetamide (10.1 g, 53.66 mmol) was suspended in 20% aqueous sodium hydroxide (38 mL, 188 mmol) and stirred at reflux for 22 h under nitrogen protection. Upon completion of the reaction, the dark-colored reaction solution was cooled to room temperature, diluted with water (200 mL), and washed with ethyl acetate (2 × 50 mL). The aqueous phase was adjusted to pH 5 with concentrated hydrochloric acid and subsequently extracted with ethyl acetate (2 x 100 mL). The aqueous phase was continued to be adjusted to pH 4 with concentrated hydrochloric acid and again extracted with ethyl acetate (2 × 50 mL). All organic phases were combined, washed with saturated saline (50 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residual solid was ground with petroleum ether, filtered, and the filter cake was washed with petroleum ether and dried in vacuum to obtain a beige solid 4-amino-3-ethylbenzoic acid (7.49 g, 84.5% yield) with good purity.
References
[1] Patent: US2011/190267, 2011, A1. Location in patent: Page/Page column 55-56
4-Amino-3-ethylbenzoic acid Preparation Products And Raw materials
Raw materials
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