3-메틸-1-페닐-2-피라졸린-5-온

3-메틸-1-페닐-2-피라졸린-5-온
3-메틸-1-페닐-2-피라졸린-5-온 구조식 이미지
카스 번호:
89-25-8
한글명:
3-메틸-1-페닐-2-피라졸린-5-온
동의어(한글):
3-메틸-1-페닐-2-피라졸린-5-온;3-메틸-1-페닐-5-피라졸론;3-메틸-1-페닐-5-피라졸론및그염류(예:페닐메틸피라졸론);페닐메틸피라졸론
상품명:
5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one
동의어(영문):
PMP;EDARAVONE;1-Phenyl-3-methyl-5-pyrazolone;5-METHYL-2-PHENYL-2,4-DIHYDRO-3H-PYRAZOL-3-ONE;3-methyl-1-phenyl-1H-pyrazol-5(4H)-one;Norphenazone;3-METHYL-1-PHENYL-5-PYRAZOLONE;3-METHYL-1-PHENYL-2-PYRAZOLIN-5-ONE;MONOPYRAZOLONE;PHENYLMETHYLPYRAZOLON
CBNumber:
CB1287462
분자식:
C10H10N2O
포뮬러 무게:
174.2
MOL 파일:
89-25-8.mol
MSDS 파일:
SDS

3-메틸-1-페닐-2-피라졸린-5-온 속성

녹는점
126-128 °C(lit.)
끓는 점
287 °C265 mm Hg(lit.)
밀도
1,12 g/cm3
증기압
0.016Pa at 20℃
굴절률
1.6300 (estimate)
인화점
191°C/17mm
저장 조건
2-8°C
용해도
3.30g/L
산도 계수 (pKa)
2.73±0.50(Predicted)
물리적 상태
결정성 분말
색상
노란색에서 베이지색
수소이온지수(pH)
4.0-4.4 (H2O, 20℃)(saturated aqueous solution)
수용성
3g/L(20℃)
Merck
14,6713
BRN
609575
안정성
제공된 대로 구매일로부터 2년 동안 안정적입니다. DMSO 또는 에탄올 용액은 -20°에서 최대 3개월 동안 보관할 수 있습니다.
InChIKey
QELUYTUMUWHWMC-UHFFFAOYSA-N
LogP
0.75 at 24℃
CAS 데이터베이스
89-25-8(CAS DataBase Reference)
NIST
3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-2-phenyl-(89-25-8)
EPA
1-Phenyl-3-methyl-5-pyrazolone (89-25-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36
WGK 독일 1
RTECS 번호 UQ9625000
TSCA Yes
HS 번호 29331990
유해 물질 데이터 89-25-8(Hazardous Substances Data)
독성 LD50 orl-rat: 3500 mg/kg LONZA# 08FEB79
기존화학 물질 KE-10718
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
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P337+P313 눈에 대한 자극이 지속되면 의학적인 조치· 조언를 구하시오.
NFPA 704
1
2 0

3-메틸-1-페닐-2-피라졸린-5-온 MSDS


Edaravone

3-메틸-1-페닐-2-피라졸린-5-온 C화학적 특성, 용도, 생산

개요

Edaravone was marketed in Japan for improving neurologic recovery following acute brain infarction. Currently, several agents classified as neuroprotectants and acting by diverse mechanisms (inhibition of glutamate release, blockade of calcium channels, lazaroids) have been marketed for treating the outcomes of brain damage due to trauma, ischemia or cardiac arrest. Edavarone is the first antioxidant with free radical scavenging activity to be introduced for this pathology. This previously described molecule (in particular as norantipyrine, one of three metabolites of antipyrine in mammals) can be simply prepared by direct cyclization of phenylhydrazine with alkylacetoacetate. Edarevone is a lipophilic agent, readily accessible to brain tissue, that is capable of reducing edema in the brain following ischemia by blocking the arachidonic acid cascade triggering peroxidative neurodegeneration. Interestingly, this agent has been shown to quench active oxygen species in endothelial cell homogenate, as well as inhibiting in vitro lipid peroxidative disintegration of membranes, so making this compound effective during reperfusion following ischemic injury. As an additional indication, phase III trials started with edaravone for increasing the chance of recovery after subarachnoid hemorrhage.

화학적 성질

Off white to light yellow powder

용도

Edaravone inhibits the disease activity in rheumatoid arthritis.

정의

ChEBI: A pyrazolone that is 2,4-dihydro-3H-pyrazol-3-one which is substituted at positions 2 and 5 by phenyl and methyl groups, respectively.

일반 설명

A free radical scavenger and antioxidant that reduces post-ischemic brain injury. Inhibits iron-dependent peroxidation in rat brain homogenates (IC50 = 15 μM). Inhibits mitochondrial permeability transition pore.

위험도

Toxic by ingestion.

생물학적 활성

A radical scavenger and antioxidant which is able to protect against the effects of ischemia, probably by inhibiting the lipoxygenase system. Protects against MPTP-induced neurotoxicity.

Safety Profile

Moderately toxic by ingestion andintraperitoneal routes. An eye irritant. When heated todecomposition it emits toxic fumes of NOx.

Purification Methods

Crystallise the pyrazolone from hot H2O, EtOH or EtOH/water (1:1). It complexes with metals. [Veibel et al. Acta Chim Scand 6 1066 1952, Beilstein 24 II 9, 24 III/IV 71.]

3-메틸-1-페닐-2-피라졸린-5-온 준비 용품 및 원자재

원자재

준비 용품


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