721-50-6

  • Product Name:Prilocaine
  • Molecular Formula:C13H20N2O
  • Purity:99%
  • Molecular Weight:
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Product Details

Appearance:White crystalline powder

Hot Sale, best quality Prilocaine 721-50-6

  • Molecular Formula:C13H20N2O
  • Molecular Weight:220.315
  • Appearance/Colour:White crystalline powder 
  • Melting Point:37-38oC 
  • Refractive Index:nD20 1.5298 
  • Boiling Point:361.6 °C at 760 mmHg 
  • PKA:pKa 7.32 or 7.89 (Uncertain) 
  • Flash Point:134.3 °C 
  • PSA:41.13000 
  • Density:1.029 g/cm3 
  • LogP:2.78550 

top purity Prilocaine 721-50-6 Usage

Prilocaine is a secondary amide analogue of lidocaine, belongs to amide local anesthetic drug with its anesthesia intensity and speed being similar as lidocaine, which is clinically for local anesthesia, especially suitable for treating patients who are not allowed to use adrenaline. It has a better clinical performance in terms of providing rapid dental anesthesia and earlier teeth extraction than lidocaine. 

Definition

ChEBI: An amino acid amide in which N-propyl-DL-alanine and 2-methylaniline have combined to form the amide bond; used as a local anaesthetic.

InChI:InChI=1/C13H20N2O/c1-4-9-14-11(3)13(16)15-12-8-6-5-7-10(12)2/h5-8,11,14H,4,9H2,1-3H3,(H,15,16)

721-50-6 Relevant articles

Prilocaine: Mechanisms and application

Naresh Kumar Katari , Sreekantha B. Jonnalagadda 

Treatments, Mechanisms, and Adverse Reactions of Anesthetics and Analgesics 2022, Pages 151-164

This review describes the physical and chemical characteristics of prilocaine, and different liposomes loaded with prilocaine, their antibacterial activity, and clinical aspects of intrathecal prilocaine.

Thermal investigation on hydrated co-amorphous systems of nicotinamide and prilocaine

Xiaoyue Xu, Thomas Rades, Holger Grohganz

European Journal of Pharmaceutics and Biopharmaceutics Volume 186, May 2023, Pages 1-6

Recent studies showed that water can also act as an anti-plasticizer that reduced the molecular mobility of prilocaine (PRL), resulting in a higher Tg of hydrated PRL compared with that of anhydrous, amorphous PRL [14], [15]. The nature of the anti-plasticizing effect has not been finally elucidated, but it is speculated to be due to the interaction of water with the dimer structure of PRL [14].

721-50-6 Process route

propylamine
107-10-8,42939-71-9

propylamine

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

<i>o</i>-toluidine
95-53-4

o-toluidine

prilocaine
721-50-6,14289-31-7

prilocaine

Conditions
Conditions Yield
2-chloropropionyl chloride; o-toluidine; With potassium carbonate; In acetone; at 0 - 30 ℃; for 5h;
propylamine; In acetone; at 70 ℃; for 14h;
97%
propylamine
107-10-8,42939-71-9

propylamine

N-(2-methylphenyl)-2-chloropropanamide
19281-31-3

N-(2-methylphenyl)-2-chloropropanamide

prilocaine
721-50-6,14289-31-7

prilocaine

Conditions
Conditions Yield
With potassium carbonate; In acetone; Reflux;
90%

721-50-6 Upstream products

  • 107-10-8
    107-10-8

    propylamine

  • 19281-31-3
    19281-31-3

    N-(2-methylphenyl)-2-chloropropanamide

  • 7623-09-8
    7623-09-8

    2-chloropropionyl chloride

  • 95-53-4
    95-53-4

    o-toluidine

721-50-6 Downstream products

  • 521964-99-8
    521964-99-8

    C42H70O35*C13H20N2O

  • 1786-81-8
    1786-81-8

    prilocaine hydrochloride

  • 14289-31-7
    14289-31-7

    D(-)-α-Propylamino-2-methyl-propioanilid

  • 14289-31-7
    14289-31-7

    L(+)-α-Propylamino-2-methyl-propioanilid