| Identification | More | [Name]
DL-ADRENALINE HYDROCHLORIDE | [CAS]
329-63-5 | [Synonyms]
4-[1-HYDROXY-2-(METHYLAMINO)ETHYL]-1,2-BENZENEDIOL HYDROCHLORIDE
(+/-)-ADRENALIN HYDROCHLORIDE
DL-1-(3,4-DIHYDROXYPHENYL)-2-METHYLAMINOETHANOL HYDROCHLORIDE
DL-3,4-DIHYDROXY(1-HYDROXY-2-METHYLAMINOETHYL)BENZENE HYDROCHLORIDE
DL-3,4-DIHYDROXY-ALPHA-[(METHYLAMINO)METHYL]BENZYL ALCOHOL HYDROCHLORIDE
DL-ADRENALINE HYDROCHLORIDE
DL-EPINEPHRINE HYDROCHLORIDE
(+/-)-EPINEPHRINE HYDROCHLORIDE
RACEMIC EPINEPHRINE HYDROCHLORIDE
RAC EPINEPHRINE HCL
TIMTEC-BB SBB003360
(+-)-adrenalinehydrochloride
4-(1-hydroxy-2-(methylamino)ethyl)-,hydrochloride,(+-)-2-benzenediol
4-[1-hydroxy-2-(methylamino)ethyl]-,hydrochloride,(+/-)-2-benzenediol
benzylalcohol,3,4-dihydroxy-alpha-((methylamino)methyl)-,hydrochloride,(+-)
epinephrinehydrochloride(racepinephrinehydrochloride)
(±)-4-[1-hydroxy-2-(methylamino)ethyl]pyrocatechol hydrochloride
Adrenaline Hcl， racepinephrine hcl
1,2-Benzenediol, 4-1-hydroxy-2-(methylamino)ethyl-, hydrochloride
rs-epinephrine hcl | [EINECS(EC#)]
206-346-0 | [Molecular Formula]
C9H14ClNO3 | [MDL Number]
MFCD00050562 | [Molecular Weight]
219.67 | [MOL File]
329-63-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
R24/25:Toxic in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2811 6.1/PG 2
| [WGK Germany ]
3
| [RTECS ]
DO3330000
| [HazardClass ]
6.1(a) | [PackingGroup ]
II | [HS Code ]
2937901500 |
| Hazard Information | Back Directory | [Chemical Properties]
solid | [Uses]
An adrenergic receptor agonist. | [Uses]
bronchodilatator, | [General Description]
Epinephrine (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. | [Biochem/physiol Actions]
Epinephrine improves systemic pressure during cardiopulmonary resuscitation and is used post cardiac arrest. The levels of epinephrine increases during trauma, sepsis and hypoglycemia resulting in increased cardiac rate and contractility. It is used in the treatment of acute anaphylaxis. Use of epinephrine hydrochloride enables dilation of pupil during intraocular lens (IOL) implantation surgery. |
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