메프로바메이트

메프로바메이트
메프로바메이트 구조식 이미지
카스 번호:
57-53-4
한글명:
메프로바메이트
동의어(한글):
메프로바메이트
상품명:
Meprobamate
동의어(영문):
Erina;Dapaz;Diron;Klort;Letyl;CaMHA;Oasil;paxin;Seril;Urbil
CBNumber:
CB6477952
분자식:
C9H18N2O4
포뮬러 무게:
218.25
MOL 파일:
57-53-4.mol
MSDS 파일:
SDS

메프로바메이트 속성

녹는점
97-100°C
끓는 점
358.93°C (rough estimate)
밀도
1.2004 (rough estimate)
굴절률
1.4480 (estimate)
인화점
11 °C
저장 조건
2-8°C
용해도
DMF: 50 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 30 mg/ml; Ethanol: 25 mg/ml
산도 계수 (pKa)
13.09±0.50(Predicted)
수용성
6.2g/L(25℃)
안정성
안정적인. 타기 쉬운. 강한 산화제와 호환되지 않습니다.
CAS 데이터베이스
57-53-4(CAS DataBase Reference)
NIST
1,3-Propanediol, 2-methyl-2-propyl-, dicarbamate(57-53-4)
EPA
Meprobamate (57-53-4)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,T,F
위험 카페고리 넘버 22-39/23/24/25-23/24/25-11
안전지침서 7-16-36/37-45
유엔번호(UN No.) UN 1230 3/PG 2
WGK 독일 3
RTECS 번호 TZ0175000
HS 번호 2924110000
유해 물질 데이터 57-53-4(Hazardous Substances Data)
독성 LD50 i.p. in mice: 800 mg/kg (Berger)
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
NFPA 704
0
1 0

메프로바메이트 MSDS


2-Methyl-2-propylpropane-1,3-diol dicarbamate

메프로바메이트 C화학적 특성, 용도, 생산

화학적 성질

white crystalline powder

용도

An anxiolytic. This is a controlled substance.

World Health Organization (WHO)

Meprobamate, a bis-carbamate ester, was introduced in 1955 for the treatment of anxiety and was subsequently used as a sedative-hypnotic drug. Psychological and physical dependence can occur and abuse has been reported. Meprobamate is controlled under Schedule IV of the 1971 Convention on Psychotropic Substances. (Reference: (UNCPS4) United Nations Convention on Psychotropic Substances (IV), , , 1971)

일반 설명

Meprobamate,2-methyl-2-propyltrimethylene dicarbamate, 2-methyl-2-propyl-1,3-propanediol dicarbamate (Equanil, Miltown), is officiallyindicated as an antianxiety agent. It is also a sedative–hypnotic agent. It has several overall pharmacological properties resembling those of benzodiazepines and barbiturates.The mechanism of action underlying anxiolytic effectsis unknown but may involve effects on conductivity inspecific brain areas.It does not appear to act through effectson GABAergic systems.The drug is effective againstabsence seizures and may worsen generalized tonic–clonicseizures.

공기와 물의 반응

Insoluble in water.

반응 프로필

Meprobamate is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.

위험도

Central nervous system depressant, use restricted by law.

화재위험

Flash point data for Meprobamate are not available; however, Meprobamate is probably combustible.

Clinical Use

Meprobamate is also a centrally acting skeletal musclerelaxant. The agents in this group find use in several conditions,such as strains and sprains that may produce acutemuscle spasm. They have interneuronal blocking propertiesat the level of the spinal cord, which are said to bepartly responsible for skeletal muscle relaxation.Also,the general CNS depressant properties they possess maycontribute to, or be mainly responsible for, the skeletalmuscle relaxant activity.

Safety Profile

Human poison by unspecified routes. Moderately toxic to humans and experimentally by ingestion. Experimental poison by intravenous, intraperitoneal, and subcutaneous routes. An experimental teratogen. Human systemic effects by ingestion: coma, blood pressure decrease, regional or general arteriolar constriction, dyspnea, cyanosis, respiratory depression, nausea or vomiting, and allergic skin dermatitis. Experimental reproductive effects. Mutation data reported. Implicated in aplastic anemia. Used as a tranquilizer. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Crystallise it from hot water, aqueous EtOH (m 104-105.5o) or xylene (m 104.1-105.3o). It can be an addictive drug. [Beilstein 3 IV 73.]

메프로바메이트 준비 용품 및 원자재

원자재

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