Prilocaine

HCID 4906CAS 721-50-6

Basic information

Standard SMILES
CCCNC(C)C(=O)Nc1ccccc1C
InChIKey
MVFGUOIZUNYYSO-UHFFFAOYSA-N
Molecular formula
C13H20N2O
Average molar mass
220.31 g/mol
Monoisotopic mass
220.15756326

Overview

Prilocaine is 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. It has a role as an anticonvulsant and a local anaesthetic. It is an amino acid amide and a monocarboxylic acid amide.

Names & identifiers

Preferred name
Prilocaine
IUPAC
N-(2-methylphenyl)-2-(propylamino)propanamide
English name
Prilocaine
Molecular formula
C13H20N2O
Molecular weight
220.31

Names & synonyms

prilocaine721-50-6Propitocaineprilocaine basePrilocainaPrilocainumAstra 1515N-(2-Methylphenyl)-2-(propylamino)propanamideo-Methyl-2-propylaminopropionanilidePropanamide, N-(2-methylphenyl)-2-(propylamino)-o-Propionotoluidide, 2-(propylamino)-2-(Propylamino)-o-propionotoluidide
Show more names
Aβ25-35l67PrilocainCitanestPrilocaine Free Base2-(PropylaMino)-N-(o-tolyl)propanaMideN-(2-methylphenyl)-2-(propylamino)propionamideL 67
Astra 1512o-Methyl-alpha-propylaminopropionanilide2-Methyl-alpha-propylaminopropionanilidealpha-n-Propylamino-2-methylpropionanilideNSC-40027ASTRA-1512ASTRA-1515CHEBI:8404

Database identifiers

CAS
721-50-6
PubChem CID
4906
DTXSID
DTXSID7031955
ChEMBL
CHEMBL1194
ChEBI
CHEBI:8404
UNII
046O35D44R
EC Number
211-957-0
Nikkaji
J6.949C

Properties

Computed structural properties

XLogP
2.1
Topological polar surface area
41.1 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
2
Rotatable bonds
5
Heavy atoms
16

Experimental & physicochemical properties

DrugsPharmaceuticals
LogP · 3 items

log Kow= 2.11

2.1

2.11

OdorODORLESS
TasteINITIALLY ACID & THEN BITTER TASTE
Color/Form · 2 items

Needles

WHITE

Solubility · 4 items

Crystals from ethanol + isopropyl ether; readily sol in water; mp 167-168 °C /Hydrochloride/

FREELY SOL IN ALC; SLIGHTLY SOL IN CHLOROFORM

VERY SLIGHTLY SOL IN ACETONE; PRACTICALLY INSOL IN ETHER

3.26e-01 g/L

Physicochemical properties

Melting point
37 · 37-38°
Boiling point
0.1 · bp0.1 159-162°
Density
1.0117 · 1.0117 (rough estimate)
refractive index
20 · nD20 1.5298
storage temp.
2 · 2-8°C
solubility
Slightly soluble in water, very soluble in acetone and in ethanol (96 per cent).

Safety & regulation

GHS classification

GHS Classification · 4 items

Warning

H302 (98.6%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P264+P265, P270, P273, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 69 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory InformationPropanamide, N-(2-methylphenyl)-2-(propylamino)-: Does not have an individual approval but may be used under an appropriate group standard
Other Safety InformationIMAP assessments - Propanamide, N-(2-methylphenyl)-2-(propylamino)-: Environment tier I assessment
FDA Requirements · 1 item

Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).

Hazard Classes and CategoriesAcute Tox. 4 (98.6%)

Safety & protection

Disposal Methods · 1 item

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Toxicology

Interactions · 5 items

...MOUSE TRIALS INDICATE INCR TOXICITY WHEN COMBINED WITH TETRACAINE.

...PRILOCAINE...REPORTED TO INTERACT WITH SUCCINYLCHOLINE /RESULTING IN INCR IN INTENSITY & DURATION OF SUCCINYLCHOLINE-INDUCED NEUROMUSCULAR BLOCKADE & RESP DEPRESSION; OTHER DEPOLARIZING MUSCLE RELAXANTS (EG DECAMETHONIUM) & NONDEPOLARIZING MUSCLE RELAXANTS (EG GALLAMINE TRIETHIODIDE & PANCURONIUM) MAY BEHAVE SIMILARLY/.

.../PRILOCAINE/ PRODUCED A SLIGHT INCR IN INTENSITY OF NEUROMUSCULAR BLOCKADE /OF ALCURONIUM CHLORIDE/. ...MARKED DECR IN TIDAL VOL, INDICATING RESP DEPRESSION, WAS OBSERVED...

EPINEPHRINE PROLONGS THE EFFECT /OF PRILOCAINE/. /PRILOCAINE HCL/

For more Interactions (Complete) data for PRILOCAINE (15 total), please visit the HSDB record page.

Non-Human Toxicity Excerpts...CAPABLE OF INDUCING METHEMOGLOBINEMIA IN LAB ANIMALS... /PRILOCAINE HCL/
Antidote and Emergency TreatmentALTHOUGH METHEMOGLOBINEMIA IS READILY REVERSED BY THE IV ADMIN OF METHYLENE BLUE ... THE THERAPEUTIC EFFECT MAY BE SHORT-LIVED BECAUSE METHYLENE BLUE MAY BE CLEARED BEFORE CONVERSION OF ALL THE METHEMOGLOBIN TO HEMOGLOBIN. /PRILOCAINE HCL/
Effects During Pregnancy and Lactation · 2 items

◉ Summary of Use during Lactation

◈ What is prilocaine?

Regulatory information

FDA Requirements · 1 item

Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).

Safety data

wgk
WGK 3
hs_code
2924296000
Signal word
Warning
Symbol(GHS)
GHS07
Storage Class
11 - Combustible Solids
Hazard statements
H302-H319

Chemistry & industry

Pharmacology

ATC Code · 3 items

N01BB04

N - Nervous system

QN - Nervous system

Protein BindingPrilocaine is 55% protein bound in plasma at a concentraion of 0.5-1.0 mg/mL.
Pharmacodynamics · 1 item

Prilocaine binds to the intracellular surface of sodium channels which blocks the subsequent influx of sodium into the cell. Action potential propagation and nerve function is, therefore, prevented. This block is reversible and when the drug diffuses away from the cell, sodium channel function is restored and nerve propagation returns.

Mechanism of Action · 5 items

Prilocaine acts on sodium channels on the neuronal cell membrane, limiting the spread of seizure activity and reducing seizure propagation. The antiarrhythmic actions are mediated through effects on sodium channels in Purkinje fibers.

... BLOCK CONDUCTION IN NERVE PERHAPS BY COMPETING WITH CA @ SOME SITE THAT CONTROLS PERMEABILITY OF MEMBRANE ... CA IS ALSO INVOLVED IN ACTION OF LOCAL ANESTHETICS ON SMOOTH MUSCLE ... & ON ADRENAL MEDULLA ... /LOCAL ANESTHETICS/

... PREVENT THE GENERATION & THE CONDUCTION OF THE NERVE IMPULSE. THEIR PRIMARY SITE OF ACTION IS THE CELL MEMBRANE. ... BLOCK CONDUCTION BY DECREASING OR PREVENTING THE LARGE TRANSIENT INCREASE IN THE PERMEABILITY OF EXCITABLE MEMBRANES TO NA+ THAT NORMALLY IS PRODUCED BY A SLIGHT DEPOLARIZATION OF THE MEMBRANE. /LOCAL ANESTHETICS/

AS ANESTHETIC ACTION PROGRESSIVELY DEVELOPS IN A NERVE, THRESHOLD FOR ELECTRICAL EXCITABILITY INCR & SAFETY FACTOR FOR CONDUCTION DECR; WHEN THIS ACTION IS SUFFICIENTLY WELL-DEVELOPED, BLOCK OF CONDUCTION IS PRODUCED. /LOCAL ANESTHETICS/

.../2 POSSIBILITIES:/ ACHIEVE BLOCK BY INCR SURFACE PRESSURE OF LIPID LAYER THAT CONSTITUTES NERVE MEMBRANE...CLOSING PORES THROUGH WHICH IONS MOVE. ... /OR:/ AFFECT PERMEABILITY BY INCR DEGREE OF DISORDER OF MEMBRANE. /LOCAL ANESTHETICS/

Biological Half-Life · 1 item

MEPIVACAINE-HCL (I-HCL) & PRILOCAINE-HCL (II-HCL) WERE INFUSED IV 250 MG INTO HEALTHY VOLUNTEERS. T/2 FOR I WAS GENERALLY LONGER THAN II; TOTAL BODY CLEARANCE II CONSISTENTLY GREATER THAN I. II CLEARANCE EXCEEDED NORMAL HEPATIC BLOOD FLOW: EXTRA-HEPATIC METAB SITE IS POSTULATED.

Metabolism/Metabolites · 2 items

The amide-linked local anesthetics are, in general, degraded by the hepatic endoplasmic reticulum, the initial reactions involving N-dealkylation and subsequent hydrolysis. However, with prilocaine, the initial step is hydrolytic, forming o-toluidine metabolites that can cause methemoglobinemia.

BIOTRANSFORMATION OF PRILOCAINE...IN RATS GAVE O-TOLUIDINE & N-PROPYLALANINE.

Uses & manufacturing

Uses · 4 items

MEDICATION (VET)

MEDICATION

Local anesthetic

Use (kg; approx.) in Germany (2009): >1000

Methods of Manufacturing · 2 items

O-TOLUIDINE IS CONDENSED WITH 2-BROMOPROPIONYL BROMIDE & RESULTING 2-BROMO-O-PROPIONOTOLUIDIDE IS IN TURN CONDENSED WITH PROPYLAMINE TO YIELD PRILOCAINE (BASE). AN ACETONE SOLN OF BASE TREATED WITH HCL YIELDS THE OFFICIAL SALT. /PRILOCAINE HCL/

Prilocaine is synthesized by reacting 2-aminotoluene with 2-bromopropionyl chloride and then with n-propylamine. /Hydrochloride/

Use ClassificationPharmaceuticals
General Manufacturing InformationIt has a pharmacological profile similar to that of lidocaine.
Applications · 4 items

UsesIt is a kind of local anesthetic drug. The product has better efficacy than procaine and the local anesthesia intensity and speed being similar as lidocaine but with longer duration time and less toxicity as well as smaller accumulation effect. It is suitable for epidural anesthesia, conduction anesthesia and infiltration anesthesia.

UsesPrilocaine is a local anesthetic of the amino amide type. Prilocaine is often used in dentistry. Prilocaine is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA), for treatment of conditions like paresthesia.

UsesIn terms of pharmacological parameters, prilocaine is comparable to lidocaine; however, because of a number of toxic manifestations, it is rarely used in medical practice. Citanest and xylonest are well-known synonyms for prilocaine.

General DescriptionPrilocaine hydrochloride is a water-soluble salt available asa solution for nerve block or infiltration in dental procedures.Prilocaine is used for intravenous regional anesthesiaas the risk of CNS toxicity is low because of the quick metabolism.Prilocaine prepared in the crystal form is used inEMLA for topical administration to decrease painful needlesticks in children. Prilocaine 4% solution should be protectedfrom light and the manufacturer recommends discardingif the solution turns pinkish or slightly darker than lightyellow. Solutions are available in various concentrations upto 4%, with or without epinephrine and with or withoutpreservatives.

Suppliers50 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
Shanghai Biolang Biotechnology Co., Ltd.+86-15970428662 +86-13397199602 · [email protected]
江苏瑞点药业有限公司15896106238 · [email protected]

Additional notes

DefinitionChEBI: 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.

Related reactions

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