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MEPERIDINE

MEPERIDINE Structure
CAS No.
57-42-1
Chemical Name:
MEPERIDINE
Synonyms
Lydol;C07128;Dolsin;Demarol;Demerol;Nemerol;Petydyna;Pethidin;Pethanol;Petantin
CBNumber:
CB1121049
Molecular Formula:
C15H21NO2
Molecular Weight:
247.33
MOL File:
57-42-1.mol
Modify Date:
2023/5/4 17:34:40

MEPERIDINE Properties

Melting point 270°C
Boiling point 390.37°C (rough estimate)
Density 1.0267 (rough estimate)
refractive index 1.5130 (estimate)
Flash point 11 °C
storage temp. −20°C
pka pKa 8.7 (Uncertain)
Water Solubility 6.55g/L(25 ºC)
BCS Class 1
EPA Substance Registry System 4-Piperidinecarboxylic acid, 1-methyl-4-phenyl-, ethyl ester (57-42-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS06,GHS08
Signal word  Danger
Hazard statements  H225-H301+H311+H331-H370
Precautionary statements  P210-P260-P280-P301+P310-P311
Hazard Codes  F,T
Risk Statements  11-23/24/25-39/23/24/25
Safety Statements  7-16-36/37-45
RIDADR  UN 1230 3/PG 2
WGK Germany  1
Toxicity A narcotic analgesic used for moderate to severe pain and during obstetrical anesthesia. Its oral LD50 in rats is 170 mg/kg. It has multiple actions qualitatively similar to those of morphine, and therapy is similar to that for morphine. Advantages over morphine concerning efficacy and reduced risk of addiction were largely illusory. This, and potential drug interactions, have resulted in a dramatic reduction in use.

MEPERIDINE Chemical Properties,Uses,Production

Uses

Analgesic (narcotic).

Biological Functions

Meperidine (Demerol) is a phenylpiperidine derivative of morphine that was developed in the late 1930s as a potential anticholinergic agent. It has some anticholinergic side effects that lead to tachycardia, blurred vision, and dry mouth. Meperidine is approximately onefifth as potent as morphine and is absorbed only half as well when administered orally as parenterally. It has a rapid onset and short duration of action (2 hours), that is, approximately one-fourth that of morphine.
Like morphine, meperidine has an active metabolite, normeperidine, formed by N-demethylation of meperidine. Normeperidine is not analgesic but is a proconvulsant and a hallucinogenic agent. For this reason, meperidine use in patients with renal or liver insufficiency is contraindicated because of the decreased clearance of the drug and its metabolite. Convulsant activity has been documented in elderly patients given meperidine and in patients using PCA who have decreased renal function.
Meperidine differs from morphine in that it has far less antitussive effect and little constipative effect. The drug is particularly useful in cancer patients and in pulmonary patients, in whom the cough reflex must remain intact. However, it does have more seizure-inducing activity than morphine. Although meperidine produces spasms of the biliary tract and colon, such spasms are of shorter duration than those produced by morphine.
Meperidine readily passes the placenta into the fetus. However, respiratory depression in the newborn has not been observed, and meperidine clearance in the newborn is rapid in that it does not rely upon conjugation to glucuronides. Meperidine, unlike morphine, has not been associated with prolongation of labor; conversely, it increases uterine contractions.

General Description

Meperidine (Demerol) was discovered in 1939 during a serendipitous screening of compounds being studied for antispasmodic activity. Mice given meperidine were noted to carry their tails in an erect position (the Straub tail reaction), which was indicative of narcotic analgesia. This led to the study of meperidine and derivatives as analgesic agents. Meperidine was found to have low potency at the receptor compared with morphine (0.2%) but much higher penetration into the brain resulting in a compound with about 10% of the potency of morphine.
Structural changes that increase the potency of meperidine include the introduction of an mhydroxyl on the phenyl ring, substituting the methyl on the N for a phenylethyl or a p-aminophenylethyl. Replacing the N-methyl with an N-allyl or N-cyclopropylmethyl group does not generate an antagonist, unlike the similar substitution of the morphine congeners. Meperidine quickly penetrates the blood-brain barrier and thus has a quick onset of activity and a high abuse potential.

Precautions

Contraindications are similar to those of morphine. In addition, because normeperidine accumulates in renal dysfunction and meperidine accumulates in hepatic dysfunction, meperidine is contraindicated in such patients because of convulsant effects. Similarly, the use of meperidine is contraindicated in patients who have a history of seizures or who are taking medication to prevent seizures. Phenytoin administered for seizures may reduce the effectiveness of meperidine by increasing the metabolism of the drug in the liver. Meperidine is not generally used in patients with cardiac dysfunction, since its anticholinergic effects can increase both heart rate and ectopic beats.

MEPERIDINE Preparation Products And Raw materials

N-Methyl-4-phenyl-4-carbethoxypiperidine Petantin Pethanol Pethidin Pethidine Pethidineter Petydyna Phetidine Piperosal Pipersal Mepergan Pamergan Mepridine 4-Piperidinecarboxylic acid, 1-methyl-4-phenyl-, ethyl ester PETHIDINEHCL(DANGEROUSDRUG) PETHIDINE/MEPERIDINE Meperidine solution C07128 Methanol(test Meperidine,1.0mg/mL) 1-methyl-4-phenyl-4-piperidinecarboxylicaciethylester 1-Methyl-4-phenylisonipecotic acid, ethyl ester 1-methyl-4-phenylisonipecoticacid,ethylester 1-methyl-4-phenylisonipecoticacidethylester 1-methyl-4-phenyl-isonipecoticaciethylester 1-Methyl-4-phenyl-piperidin-4-carbon-saeure-aethylester 1-Methyl-4-phenylpiperidine-4-carboxylic acid ethyl ester 1-methyl-4-phenylpiperidine-4-carboxylicacidethylester Demarol Demerol Dolantin Dolsin Ethyl 1-methyl-4-phenyl-4-piperidinecarboxylate Ethyl 1-methyl-4-phenylisonipecotate Ethyl 1-methyl-4-phenylpiperidine-4-carboxylate MEPERIDINE 1-Methyl-4-phenyl-4-piperidinecarboxylic acid ethyl ester 1-methyl-4-phenyl-4-piperidinecarboxylicacidethylester ethyl1-methyl-4-phenylisonipecotate ethyl1-methyl-4-phenylpiperidine-4-carboxylate Isonipecaine Isonipecotic acid, 1-methyl-4-phenyl-, ethyl ester Lydol Meperidine (demerol)) Meperidol Methyl phenylpiperidine carbonic acid ethyl ester methylphenylpiperidinecarbonicacidethylester Nemerol XADCESSVHJOZHK-UHFFFAOYSA-N MEPERIDINE USP/EP/BP 57-42-1 Stable Isotopes Controlled Drug StandardsAlphabetic M MEA - MES