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Principaux documents

17809

Sigma-Aldrich

(−)-Epinephrine (+)-bitartrate salt

tested according to Ph. Eur.

Synonyme(s) :

Adrenalini tartras, L-3,4-Dihydroxy-α-(methylaminomethyl)benzyl alcohol D-hydrogen bitartrate salt, L-Adrenaline (+)-bitartrate salt, L-Adrenaline D-hydrogentartrate, L-Epinephrine D-hydrogentartrate

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About This Item

Formule empirique (notation de Hill):
C9H13NO3 · C4H6O6
Numéro CAS:
Poids moléculaire :
333.29
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352200
ID de substance PubChem :

Agence

tested according to Ph. Eur.

Niveau de qualité

Solubilité

water: soluble 1 gm in 3 ml
alcohol: slightly soluble
chloroform: insoluble
diethyl ether: insoluble

Application(s)

pharmaceutical (small molecule)

Chaîne SMILES 

O[C@H]([C@@H](O)C(O)=O)C(O)=O.CNC[C@H](O)c1ccc(O)c(O)c1

InChI

1S/C9H13NO3.C4H6O6/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;5-1(3(7)8)2(6)4(9)10/h2-4,9-13H,5H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t9-;1-,2-/m01/s1

Clé InChI

YLXIPWWIOISBDD-NDAAPVSOSA-N

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Application

(-)-Epinephrine (+)-bitartrate salt has been used for studying the active calcium uptake by rainbow trout skin. It has also been used in oxygen-derived oxidant assays for assessing the susceptibility of C. neoformans biofilms to antimicrobial molecules.

Actions biochimiques/physiologiques

(-)-Epinephrine (+)-bitartrate salt is an α,β-adrenergic receptor agonist. It inhibits the lipolysis completely and can overcome the antilipolytic impact of insulin in perifused isolated fat cell.
Adrenergic receptor agonist.

Pictogrammes

Skull and crossbones

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 1 Oral

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

S S Solomon et al.
The Journal of laboratory and clinical medicine, 88(6), 984-994 (1976-12-01)
Development of a perifusion system utilizing isolated fat cells (IFC) has converted the static incubation system into one capable of measuring dynamic changes in adipose tissue metabolism. Using this new system, we have studied the initiation by epinephrine and inhibition
Luis R Martinez et al.
Infection and immunity, 74(11), 6118-6123 (2006-10-24)
The human pathogenic fungus Cryptococcus neoformans can form biofilms on polystyrene plates and medical devices in a process that requires capsular polysaccharide release. Although biofilms are known to be less susceptible to antimicrobial drugs, little is known about their susceptibility
W S Marshall et al.
The Journal of experimental biology, 166, 297-316 (1992-05-01)
The skin overlying the cleithrum bone of freshwater-acclimated rainbow trout contains numerous mitochondria-rich (MR) cells, as detected by DASPEI fluorescence. This tissue was mounted in vitro in an Ussing-style chamber with fresh water on the mucosal surface and saline supplemented
Yangjie Wei et al.
AAPS PharmSciTech, 16(2), 455-465 (2014-11-02)
Several attempts have been made to mask the bitter taste of oral formulations, but none have been made for injectable formulations. This study aims to mask the bitter taste of dental lidocaine HCl (LID) injection using hydroxypropyl-β-cyclodextrin (HP-β-CD) and sodium
Margot Van der Jeught et al.
Cellular reprogramming, 17(3), 170-180 (2015-06-09)
In mice, inhibition of both the fibroblast growth factor (FGF) mitogen-activated protein kinase kinase/extracellular-signal regulated kinase (MEK/Erk) and the Wnt signaling inhibitor glycogen synthase-3β (GSK3β) enables the derivation of mouse embryonic stem cells (mESCs) from nonpermissive strains in the presence

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