Mepivacaine

Mepivacaine 구조식 이미지
카스 번호:
22801-44-1
상품명:
Mepivacaine
동의어(영문):
MEPIVACAINE;A pp because;MepivacaineBase;Mepivacaine USP/EP/BP;Mepivacaine Impurity A;Mepivacaine Impurity 1;Mepivacaine HCl (base);Mepivacaine hydorchloride;Trimethocaine hydrochloride;Mepivacaine(Cas number22801-44-1)
CBNumber:
CB8460318
분자식:
C15H22N2O
포뮬러 무게:
246.35
MOL 파일:
22801-44-1.mol

Mepivacaine 속성

녹는점
147-151°C
저장 조건
-20°C Freezer
용해도
클로로포름(약간 용해됨), DMSO(약간 용해됨), 에탄올(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
pKa 7.73(H2O,t =25±0.2,I=0.01(NaCl)) (Uncertain)
색상
흰색에서 황백색까지
InChI
InChI=1S/C15H22N2O/c1-11-7-6-8-12(2)14(11)16-15(18)13-9-4-5-10-17(13)3/h6-8,13H,4-5,9-10H2,1-3H3,(H,16,18)
InChIKey
INWLQCZOYSRPNW-UHFFFAOYSA-N
SMILES
N1(C)CCCCC1C(NC1=C(C)C=CC=C1C)=O
CAS 데이터베이스
22801-44-1(CAS DataBase Reference)
EPA
2-Piperidinecarboxamide, N-(2,6-dimethylphenyl)-1-methyl- (22801-44-1)

안전

Mepivacaine C화학적 특성, 용도, 생산

용도

Local anesthetic.

일반 설명

Mepivacaine hydrochloride is available in 1% to 3% solutionsand is indicated for infiltration anesthesia, dental procedures,peripheral nerve block, or epidural block. The onset of anesthesiais rapid, ranging from about 3 to 20 minutes for sensoryblock. Mepivacaine is rapidly metabolized in the liver with50% of the administered dose excreted into the bile asmetabolites. The metabolites are reabsorbed in the intestineand excreted in the kidney with only a small percentage foundin the feces. Less than 5% to 10% of the administered dose isfound unchanged in the urine. The primary metabolic productsare the N-demethylated metabolite and the 3 and 4 phenolicmetabolites excreted as their glucuronide conjugates.

Clinical Use

Mepivacaine hydrochloride [N-(2, 6-dimethylphenyl)-1-methyl 2-piperidinecarboxamide monohydrochloride] is an amino amide-type local anesthetic agent widely used to provide regional analgesia and anesthesia by local infiltration, peripheral nerve block, and epidural and caudal blocks. The pharmacological and toxicological profile of mepivacaine is quite similar to that of lidocaine, except that mepivacaine has a slightly longer duration of action and lacks the vasodilator activity of lidocaine. For this reason, it serves as an alternate choice for lidocaine when addition of epinephrine is not recommended in patients with hypertensive vascular disease.

신진 대사

Mepivacaine undergoes extensive hepatic metabolism catalyzed by CYP1A2, with only a small percentage of the administered dosage (<10%) being excreted unchanged in the urine. The major metabolic biotransformations of mepivacaine are N-dealkylation (to give the N-demethylated compound 2′,6′-pipecoloxylidide) and aromatic hydroxylations. These metabolites are excreted as their corresponding glucuronides.

Mepivacaine 준비 용품 및 원자재

원자재

준비 용품


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