Skip to Content
Merck
All Photos(1)

Key Documents

E4375

Sigma-Aldrich

(−)-Epinephrine (+)-bitartrate salt

solid, adrenergic receptor agonist

Synonym(s):

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

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H13NO3 · C4H6O6
CAS Number:
Molecular Weight:
333.29
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

product name

(−)-Epinephrine (+)-bitartrate salt, solid

form

solid

Quality Level

color

white

solubility

H2O: soluble
alcohol: soluble

storage temp.

2-8°C

SMILES string

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

InChI key

YLXIPWWIOISBDD-NDAAPVSOSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Epinephrine is a hormone, which is also termed as adrenaline. It is a monoamine and catecholamine.

Application

(-)Epinephrine (+)-bitartrate salt has been used:
  • to test the possible existence of β-adrenergic vasodilation
  • to infuse into the adipose region to minimize blood loss and tissue contamination
  • as a platelet agonist in the preparation of optimal platelet aggregometry 96-well plates
  • in the measurement of total superoxide dismutase (tSOD) enzymatic activity

Biochem/physiol Actions

Epinephrine is mainly liberated from adrenal medulla in response to stress, that is facilitated through sympathetic fibers.
Adrenergic receptor agonist.

Features and Benefits

This compound is featured on the α1-Adrenoceptors, α2-Adrenoceptors, β-Adrenoceptors and Dopamine, Norepinephrine and Epinephrine Synthesis pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Caution

Light sensitive

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 1 Oral

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Aerobic exercise training lowers platelet reactivity and improves platelet sensitivity to prostacyclin in pre-and postmenopausal women
Lundberg S, et al.
Journal of Thrombosis and Haemostasis, 15(12), 2419-2431 (2017)
Regular and moderate exercise counteracts the decline of antioxidant protection but not methylglyoxal-dependent glycative burden in the ovary of reproductively aging mice
Falone S, et al.
Oxidative Medicine and Cellular Longevity (2016)
Cells, Synapses, and Neurotransmitters
Quantitative Human Physiology (2017)
CXCL5 secreted from adipose tissue-derived stem cells promotes cancer cell proliferation
Zhao Y, et al.
Oncology Letters, 15(2), 1403-1410 (2018)
Chapter 4 - Substances Involved in Neurotransmission
Nutritional and Herbal Therapies for Children and Adolescents (2010)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service