Imipramine hydrochloride

Imipramine hydrochloride 구조식 이미지
카스 번호:
113-52-0
상품명:
Imipramine hydrochloride
동의어(영문):
g22355;imidol;ia-pram;imavate;iprogen;tofranil;deprinol;dynazina;efuranol;fujisawa
CBNumber:
CB6698241
분자식:
C19H25ClN2
포뮬러 무게:
316.87
MOL 파일:
113-52-0.mol
MSDS 파일:
SDS

Imipramine hydrochloride 속성

녹는점
168-1700C
인화점
9℃
저장 조건
2-8°C
용해도
H2O: 50 mg/mL
물리적 상태
수정 같은
색상
하얀색
수소이온지수(pH)
4.2~5.2(100g/l,25℃)
수용성
물에 용해됨
최대 파장(λmax)
260nm(lit.)
Merck
14,4920
CAS 데이터베이스
113-52-0(CAS DataBase Reference)
EPA
5H-Dibenz[b,f]azepine-5-propanamine, 10,11-dihydro-N,N-dimethyl-, monohydrochloride (113-52-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,T,F
위험 카페고리 넘버 23/25-36/38-36/37/38-22-39/23/24/25-23/24/25-11
안전지침서 7-16-24-33-45-36-26-36/37
유엔번호(UN No.) UN 1230 3/PG 2
WGK 독일 3
RTECS 번호 HO1925000
TSCA Yes
HS 번호 2933995800
독성 LD50 in mice, rats (mg/kg): 400, 490 orally; 110, 90 i.p. (Tobe)
기존화학 물질 KE-11188
그림문자(GHS): GHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H300 삼키면 치명적임 급성 독성 물질 - 경구 구분 1,2 위험 GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.
P405 밀봉하여 저장하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
0
2 0

Imipramine hydrochloride C화학적 특성, 용도, 생산

화학적 성질

White Solid

용도

Imipramine hydrochloride is used as a serotonin uptake inhibitor. It mainly used in the treatment of major depression and enuresis (inability to control urination). It has also been evaluated for use in panic disorder.

일반 설명

Imipramine hydrochloride, 5-[3-(dimethylamino)propyl]-10,11-dihydro-5H-dibenz[b,f]azepine monohydrochloride(Tofranil), is the lead compound of the TCAs. It is also a closerelative of the antipsychotic phenothiazines (replace the10–11 bridge with sulfur, and the compound is the antipsychoticagent promazine). It has weaker D2 postsynaptic blockingactivity than promazine and mainly affects amines (5-HT,NE, and DA) via the transporters. As is typical of dimethylaminocompounds, anticholinergic and sedative (central H1block) effects tend to be marked. The compound per se has a tendency toward a high 5-HT-to-NE uptake block ratio andprobably can be called a serotonin transport inhibitor(SERTI). Metabolic inactivation proceeds mainly by oxidativehydroxylation in the 2-position, followed by conjugationwith glucuronic acid of the conjugate. Urinary excretion predominates(about 75%), but some biliary excretion (up to25%) can occur, probably because of the large nonpolargrouping. Oxidative hydroxylation is not as rapid or completeas that of the more nucleophilic ring phenothiazine antipsychotics;consequently, appreciable N-demethylation occurs,with a buildup of norimipramine (or desimipramine).

Clinical Use

The demethylated metabolite is less anticholinergic, lesssedative, and more stimulatory and is a SNERI.Consequently, a patient treated with imipramine has twocompounds that contribute to activity. Overall, the effect isnonselective 5-HT versus NE reuptake.

Safety Profile

Human poison by ingestion. An experimental poison by ingestion, intravenous, subcutaneous, and intraperitoneal routes. An experimental teratogen. Human systemic effects by ingestion: sleep, somnolence, convulsions, muscle contraction or spasticity, coma, blood pressure decrease, dyspnea (difficulty in breathing), paresthesia (abnormal sensations), and kidney changes. Experimental reproductive effects. Mutation data reported. Used in the treatment of depression. When heated to decomposition it emits very toxic fumes of NO, and HCl. See also DIAZEPAM.

Imipramine hydrochloride 준비 용품 및 원자재

원자재

준비 용품


Imipramine hydrochloride 공급 업체

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