기본 정보
- CAS
329-63-5- 표준 SMILES
CNCC(O)c1ccc(O)c(O)c1.Cl- InChIKey
ATADHKWKHYVBTJ-UHFFFAOYSA-N- 분자식
- C9H14ClNO3
- 평균 분자량
- 219.66 g/mol
- 단동위원소 질량
- 219.06622099
개요
Racepinephrine Hydrochloride is an organic molecular entity.
이름 및 식별자
- 우선 이름
- (+-)-Epinephrine hydrochloride
- IUPAC
- 4-[1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol;hydrochloride
- 현지명
- DL-아드레날린염화물
- 영어명
- DL-Adrenaline hydrochloride
- 분자식
- C9H14ClNO3
- 분자량
- 219.67
이름 및 동의어
329-63-5Racepinephrine hydrochlorideAsthmanefrin(+-)-Epinephrine hydrochlorideRacepinephrine HClRacepinefrine hydrochlorideAdrenaline hydrochloride, dl-Epinephrine hydrochloride, dl-336096P2WE1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, hydrochlorideEPINEPHRINE DL-FORM HYDROCHLORIDEEPINEPHRINE,RACEMIC HYDROCHLORIDE
이름 더 보기
DL-아드레날린염화물RAC EPINEPHRINE HCLDL-EPINEPHRINE HYDROCHLORIDEDL-EpinephAdrenalin HCLAdrenaline HCLEpinephrin HClDL-adrenaline hclrs-epinephrine hclTIMTEC-BB SBB003360Racepinephrine HydrochL
1,2-Benzenediol, 4-(1-hydroxy-2-(methylamino)ethyl)-, hydrochlorideEpi-MistS2 RacepinephrineRefChem:55960S2 Racepinephrine MULTI-DOSE206-346-0DL-ADRENALINE HYDROCHLORIDE(+/-)-Epinephrine hydrochloride
데이터베이스 식별자
- CAS
물성
구조 계산 물성
- 극성 표면적
- 72.7 Ų
- 수소 결합 공여자 수
- 5
- 수소 결합 수용자 수
- 4
- 회전 가능 결합 수
- 3
- 무거운 원자 수
- 14
- 형식 전하
- 0
- 복잡도
- 154
물리화학적 성질
- 녹는점
- 157 ° · 157°
- 저장 조건
- 2 · 2-8°C
- 용해도
- 2 O: · H2O: >50 mg/mL
- 물리적 상태
- 결정성 고체
- 수용성
- 2 O: · H2O: 50mg/mL
- Merck
- 14 · 14,3619
- 안정성
- 안정적이지만 빛에 민감합니다. 산, 산 염화물, 산 무수물, 산화제와 호환되지 않습니다.
- InChI
- InChI=1S/C9H13NO3.ClH/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;/h2-4,9-13H,5H2,1H3;1H
- InChIKey
- ATADHKWKHYVBTJ-UHFFFAOYSA-N
- SMILES
- C1(C(O)CNC)=CC=C(O)C(O)=C1.Cl
- EPA
- (+-)-Epinephrine hydrochloride (329-63-5)
화학적 성질
solid
안전 및 규제
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
GHS 분류
GHS Classification
Danger
H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
Regulatory Information1,2-Benzenediol, 4-1-hydroxy-2-(methylamino)ethyl-, hydrochloride: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Hazard Classes and CategoriesAcute Tox. 3 (97.6%)
안전 데이터
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- DO3330000
- ridadr
- UN 2811 6.1/PG 2
- HS 번호
- 2937901500
- risk_code
- 24/25-36/37/38
- hazard_code
- T
- safety_code
- 26-36/37-45
- 포장분류
- II
- 위험 등급
- 6.1(a)
- Hazard Classifications
- Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 OralFlam. Liq. 2STOT SE 1
- 스토리지 클래스
- 3 - Flammable liquids
화학 및 산업
약리 정보
MeSH Pharmacological Classification
Drugs that selectively bind to and activate alpha adrenergic receptors.
Drugs that selectively bind to and activate beta-adrenergic receptors.
Agents that cause an increase in the expansion of a bronchus or bronchial tubes.
Agents that dilate the pupil. They may be either sympathomimetics or parasympatholytics.
Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters.
Drugs used to cause constriction of the blood vessels.
용도 및 제조
General Manufacturing Information1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, hydrochloride (1:1): ACTIVE
응용 분야
용도임상 심혈관 타협과 조산아에 대한 동종 요법의 널리 인정 된 치료.
용도bronchodilatator,
일반 설명Epinephrine (adrenalin) is synthesized from norepinephrine (noradrenalin) by the action of the enzyme phenylethanolamine N-methyltransferase. Epinephrine comprises 5%-10% of the total catecholamines in the central nervous system. It is a mixed α/β-adrenergic receptor agonist and stimulates these receptors. Their site of synthesis is adrenal medulla and it travels through the vascular systems. Its breakdown occurs in the central nervous system (CNS), liver and kidney.
공급사100 곳
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖南韵邦生物科技股份有限公司0731-88532326 13319508186 · [email protected]
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