PHENCYCLIDINE

PHENCYCLIDINE 구조식 이미지
카스 번호:
77-10-1
동의어(한글):
펜시클리딘
상품명:
PHENCYCLIDINE
동의어(영문):
PCP;C07575;HUMPCP;Phencylidine;PHENCYCLIDINE;PrCP active human;Phencyclidine (pcp);Pcp (phencyclidine);prolylcarboxypeptidase;Phencyclidine solution
CBNumber:
CB1310072
분자식:
C17H25N
포뮬러 무게:
243.39
MOL 파일:
77-10-1.mol

PHENCYCLIDINE 속성

녹는점
46.5℃
끓는 점
bp1.0 135-137°
밀도
0.9762 (rough estimate)
굴절률
1.5000 (estimate)
인화점
11 °C
저장 조건
−20°C
산도 계수 (pKa)
pKa 8.5 (Uncertain)
색상
무색 결정
EPA
Piperidine, 1-(1-phenylcyclohexyl)- (77-10-1)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F,T
위험 카페고리 넘버 23/24/25-39/23/24/25-11-61
안전지침서 36/37-45-16-53
유엔번호(UN No.) 2811
WGK 독일 1
위험 등급 6.1(a)
포장분류 I
유해 물질 데이터 77-10-1(Hazardous Substances Data)
독성 LD50 oral in mouse: 75mg/kg
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H225 고인화성 액체 및 증기 인화성 액체 구분 2 위험 GHS hazard pictograms P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H370 장기(또는, 영향을 받은 알려진 모든 장기를 명시)에 손상을 일으킴(노출되어도 특정 표적장기 독성을 일으키지 않는다는 결정적인 노출경로가 있다면 노출경로를 기재) 특정 표적장기 독성 - 1회 노출 구분 1 위험 GHS hazard pictograms P260, P264, P270, P307+P311, P321,P405, P501
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P260 분진·흄·가스·미스트·증기·...·스프레이를 흡입하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.
P311 의료기관(의사)의 진찰을 받으시오.

PHENCYCLIDINE C화학적 특성, 용도, 생산

용도

Anesthetic.

정의

ChEBI: A member of the class of piperidines that is piperidine in which the nitrogen is substituted with a 1-phenylcyclohexyl group. Formerly used as an anaesthetic agent, it exhibits both hallucinogenic and neurotoxic effects.

일반 설명

Phencyclidine was introduced as a dissociative anestheticfor animals. Its close structural relative ketamine is still soused and may be used in humans. In humans,PCP produces a sense of intoxication, hallucinogenic experiencesnot unlike those produced by the anticholinergic hallucinogens,and often, amnesia.
The drug affects many systems, including those of NE,DA, and 5-HT. It has been proposed that PCP (and certainother psychotomimetics) produces a unique pattern of activationof ventral tegumental area dopaminergic neurons.Itblocks glutaminergic N-methyl-D-aspartate receptors.Thisaction is the basis for many of its CNS effects. PCP itself appearsto be the active agent. The psychotic state produced bythis drug is also cited as a better model than amphetaminepsychosis for the psychotic state of schizophrenia.

Pharmacology

PCP acts as a biocide through its ability to uncouple mitochondrial oxidative phosphorylation.

Safety Profile

Poison by intraperitoneal route. Experimental reproductive effects. Caution: This is a controlled substance (depressant) listed in the U.S. Code of Federal Regulations, Title 21 Part 1308.12 (1985). The ethylamine, pyrrolidine and thiophene analogs are l

신진 대사 경로

When mice and rats are administered phencyclidine intraperitoneally, several hydroxylated metabolites are identified in the urine. A new metabolite, 1-phenyl-1- (1-piperidinyl-3-ol)cyclohexane, is identified in the urine and liver microsomal preparations.

신진 대사

Pentachlorophenolwas metabolized in rats by conjugation with glucuronic acid and eliminated as the glucuronide. P450 catalyzed oxidative dechlorination also occurred to form tetrachlorohydroquinone, and this was conjugated to form a monoglucuronide representing 27% of the dose administered. Other metabolites have been reported, including isomeric tetrachlorophenols, tetrachlorocatechol and tetrachlororesorcinol. Trace amounts of benzoquinones were also noted.
Metabolites in female rats were tetrachloromonophenols, diphenols, and hydroquinones.

PHENCYCLIDINE 준비 용품 및 원자재

원자재

준비 용품


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