94-09-7

  • Product Name:Benzoicacid, 4-amino-, ethyl ester
  • Molecular Formula:C9H11NO2
  • Purity:99%
  • Molecular Weight:
Inquiry

Product Details

Appearance:white odourless crystals

Benzocaine factory 94-09-7 Wholesaler with reasonable price

  • Molecular Formula:C9H11NO2
  • Molecular Weight:165.192
  • Appearance/Colour:white odourless crystals 
  • Vapor Pressure:0.000589mmHg at 25°C 
  • Melting Point:88-90 °C 
  • Refractive Index:1.5600 (estimate) 
  • Boiling Point:310.7 °C at 760 mmHg 
  • PKA:2.5(at 25℃) 
  • Flash Point:164.2 °C 
  • PSA:52.32000 
  • Density:1.13 g/cm>3 
  • LogP:2.02670 

Benzocaine 94-09-7 Usage

Benzocaine is a white odourless needle-like crystal, slightly soluble in water and easily soluble in organic solvents. For example: ethanol, chloroform, ether, soluble in almond oil, olive oil. Benzocaine is a local anaesthetic of the ester type with a poor solubility in water. The drug benzocaine is normally used as a topical pain reliever or as a common ingredient in cough drops. Benzocaine is used in multiple forms including lotion, gel, liquid, lozenges, and sprays. Benzocaine is a colorless trapezial crystal. Its melting point is 92℃ (88-90℃), boiling point is 183-184°C (1.87kPa). 1g of this drug is soluble in about 2500ml water, 5ml ethanol, 2ml chloroform, 4ml ether or 30-50ml almond oil and olive oil, and it is also soluble in dilute acid. Furthermore, being a PABA derivative, it has similar allergenic properties to procaine and is contraindicated with sulfonamide antibacterial agents.

Definition

ChEBI: Benzocaine cream or solution inside the condom de-sensitises the male sexual organ to help delay ejaculation and prolong erection during intercourse. Benzocaine is a benzoate ester having 4-aminobenzoic acid as the acid component and ethanol as the alcohol component. A surface anaesthetic, it is used to suppress the gag reflex, and as a lubricant and topical anaesthetic on the larynx, mouth, nasal cavity, respiratory tract, oesophagus, rectum, urinary tract, and vagina. It has a role as a topical anaesthetic, an antipruritic drug, an allergen and a sensitiser. It is a benzoate ester and a substituted aniline.

 

Safety Profile

Poison by ingestion and intraperitoneal routes. Human systemic effects by rectal route: methemoglobinemia/carboxyhemoglobinem ia in infants. A skin irritant and a mild sensitizer.

 

Structure and conformation

Ethyl aminobenzoate, a para-aminobenzoate derivative (PABA)

InChI:InChI=1/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3/p+1

94-09-7 Relevant articles

Metal-free organic dyes containing thiadiazole unit for dye-sensitized solar cells: A combined experimental and theoretical study

Siva Kumar, Gangala,Srinivas, Kola,Shanigaram, Balaiah,Bharath, Dyaga,Singh, Surya Prakash,Bhanuprakash,Rao, V. Jayathirtha,Islam, Ashraful,Han, Liyuan

, p. 13172 - 13181 (2014)

We have designed and synthesized four new metal free D-A-π-A type dyes (9-12) with variations in their acceptor/anchor groups. The dyes exhibited good power conversion efficiency ranging from 1.95-4.12%. Among the four dyes, 9 showed the best photovoltaic performance: short-circuit current density (Jsc) of 8.50 mA cm-2, open-circuit voltage (Voc) of 645 mV and fill factor (FF) of 0.75, corresponding to an overall conversion efficiency of 4.12% under standard global AM 1.5 solar light conditions. This journal is the Partner Organisations 2014.

Kinetics of the reduction of p-nitrobenzoic acid esters in nanoreactors on the basis of sulfonated polymers

Al'Tshuler,Shkurenko,Gorlov

, p. 372 - 375 (2015)

The kinetics of the reduction of p-nitrobenzoic acid esters in nanoreactors based on sulfonated network polymers containing nanodispersed palladium was studied. The kinetic characteristics of the hydrogenation of aromatic nitro compounds were calculated.

Cyclic (Alkyl)(amino)carbene Ligand-Promoted Nitro Deoxygenative Hydroboration with Chromium Catalysis: Scope, Mechanism, and Applications

Zhao, Lixing,Hu, Chenyang,Cong, Xuefeng,Deng, Gongda,Liu, Liu Leo,Luo, Meiming,Zeng, Xiaoming

, p. 1618 - 1629 (2021/01/25)

Transition metal catalysis that utilizes N-heterocyclic carbenes as noninnocent ligands in promoting transformations has not been well studied. The preparation of several commercially available pharmaceuticals by means of this strategy highlights its potential application in medicinal chemistry.

94-09-7 Process route

Ethyl 4-bromobenzoate
5798-75-4

Ethyl 4-bromobenzoate

4,4'-triazenediyl-di-benzoic acid diethyl ester
7334-36-3

4,4'-triazenediyl-di-benzoic acid diethyl ester

diethyl biphenyl-4,4'-dicarboxylate
47230-38-6

diethyl biphenyl-4,4'-dicarboxylate

4,4'-Iminobis(benzoesaeureethylester)
53884-32-5

4,4'-Iminobis(benzoesaeureethylester)

p-aminoethylbenzoate
94-09-7

p-aminoethylbenzoate

4,4'-bis(ethoxycarbonyl)azobenzene
7250-68-2

4,4'-bis(ethoxycarbonyl)azobenzene

Conditions
Conditions Yield
With copper(l) iodide; sodium azide; N,N`-dimethylethylenediamine; In dimethyl sulfoxide; at 100 ℃; Inert atmosphere;
 
ethyl 4-nitrobenzoate
99-77-4

ethyl 4-nitrobenzoate

p-aminoethylbenzoate
94-09-7

p-aminoethylbenzoate

4,4'-bis(ethoxycarbonyl)azobenzene
7250-68-2

4,4'-bis(ethoxycarbonyl)azobenzene

4,4'-azoxy-di-benzoic acid diethyl ester
6421-04-1,34241-38-8

4,4'-azoxy-di-benzoic acid diethyl ester

Conditions
Conditions Yield
With sodium tetrahydroborate; In tetrahydrofuran; water; at 20 ℃; for 3h; Catalytic behavior;
84 %Chromat.

94-09-7 Upstream products

  • 99-77-4
    99-77-4

    ethyl 4-nitrobenzoate

  • 61273-18-5
    61273-18-5

    4-nitro-benzoic acid-(2,2,2-trichloro-ethyl ester)

  • 10367-96-1
    10367-96-1

    2-(diethylamino)ethyl 2-chloro-4-nitrobenzoate

  • 64-17-5
    64-17-5

    ethanol

94-09-7 Downstream products

  • 15716-30-0
    15716-30-0

    ethyl 4-benzoate

  • 55966-68-2
    55966-68-2

    ethyl 4-benzoate

  • 99986-15-9
    99986-15-9

    4-(2-mercapto-ethylamino)-benzoic acid ethyl ester

  • 94-32-6
    94-32-6

    ethyl 4-(N-butylamino)benzoate

Relevant Products