(±)-4-[1-Hydroxy-2-(methylamino)ethyl]brenzcatechinhydrochlorid
(+-)-Epinephrine hydrochloride
Grundinformationen
- CAS
329-63-5- Standard-SMILES
CNCC(O)c1ccc(O)c(O)c1.Cl- InChIKey
ATADHKWKHYVBTJ-UHFFFAOYSA-N- Summenformel
- C9H14ClNO3
- Durchschnittliche Molmasse
- 219,66 g/mol
- Monoisotopische Masse
- 219,06622099
Überblick
Racepinephrine Hydrochloride is an organic molecular entity.
Namen und Bezeichner
- Bevorzugter Name
- (+-)-Epinephrine hydrochloride
- IUPAC
- 4-[1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol;hydrochloride
- Lokaler Name
- (±)-4-[1-Hydroxy-2-(methylamino)ethyl]brenzcatechinhydrochlorid
- Englischer Name
- DL-Adrenaline hydrochloride
- Summenformel
- C9H14ClNO3
- Molmasse
- 219.67
Namen und Synonyme
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
Weitere Namen anzeigen
RAC 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
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 72,7 Ų
- H-Brücken-Donoren
- 5
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 14
- Formalladung
- 0
- Komplexität
- 154
Physikochemische Eigenschaften
- Schmelzpunkt
- 157 ° · 157°
- storage temp.
- 2 · 2-8°C
- Löslichkeit
- 2 O: · H2O: >50 mg/mL
- Aggregatzustand
- A crystalline solid
- Wasserlöslichkeit
- 2 O: · H2O: 50mg/mL
- Merck
- 14 · 14,3619
- Stabilität
- Stable, but light sensitive. Incompatible with acids, acid chlorides, acid anhydrides, oxidizing agents.
- 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
- CAS Datenbank
- 329 · 329-63-5(CAS DataBase Reference)
- EPA chemische Informationen
- (+-)-Epinephrine hydrochloride (329-63-5)
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
GHS-Klassifizierung
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.
Gefahrenhinweise
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%)
Sicherheitsdaten
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 2811 6.1/PG 2
- hs_code
- 2937901500
- RTECS-Nr.
- DO3330000
- risk_code
- 24/25-36/37/38
- hazard_code
- T
- safety_code
- 26-36/37-45
- hazard_class
- 6.1(a)
- packing_group
- II
- Speicherklasse
- 3 - Flammable liquids
Chemie und Industrie
Pharmakologische Informationen
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.
Verwendung und Herstellung
General Manufacturing Information1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, hydrochloride (1:1): ACTIVE
Anwendungen
Verwendenbronchodilatator,
Anbieter100 Anbieter
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]
南通飞宇生物科技有限公司0513-68819626 15152877458 · [email protected]
武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]
武汉敬康恩生物医药科技有限公司13720134139 086-15871494362 13720134139 · [email protected]
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