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A0937

Sigma-Aldrich

(±)-Norepinephrine (+)-bitartrate salt

≥97% (TLC), powder, adrenergic neurotransmitter

Synonym(s):

(±)-Arterenol (+)-bitartrate salt, (±)-Noradrenalin (+)-bitartrate salt, 1-(3,4-Dihydroxyphenyl)-2-aminoethanol (+)-bitartrate salt, 3,4-Dihydroxyphenylethanolamine (+)-bitartrate salt

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About This Item

Empirical Formula (Hill Notation):
C8H11NO3 · C4H6O6
CAS Number:
Molecular Weight:
319.26
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

product name

(±)-Norepinephrine (+)-bitartrate salt,

form

powder

SMILES string

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

InChI

1S/C8H11NO3.C5H8O5/c9-4-8(12)5-1-2-6(10)7(11)3-5;1-2(4(7)8)3(6)5(9)10/h1-3,8,10-12H,4,9H2;2-3,6H,1H3,(H,7,8)(H,9,10)/t;2-,3-/m.1/s1

InChI key

PDZZSMDCBWCGRN-GEHKUQKJSA-N

Biochem/physiol Actions

Adrenergic neurotransmitter

Features and Benefits

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

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral

Storage Class

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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’.

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Stéphanie Falcao et al.
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[Hypovolemic shock during pregnancy].
E M Shifman
Anesteziologiia i reanimatologiia, (6)(6), 63-66 (2013-05-15)
Takahiro Higuchi et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 54(7), 1142-1146 (2013-05-15)
A novel (18)F-labeled tracer, LMI1195 (N-[3-bromo-4-(3-(18)F-fluoro-propoxy)-benzyl]-guanidine), is being developed for sympathetic nerve imaging; its high specificity for neural uptake-1 mechanism has previously been demonstrated in cell associative studies and in rabbit and nonhuman primate studies assessing heart uptake. The aim
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Andreas Schwittay
MMW Fortschritte der Medizin, 155(1), 64-64 (2013-04-12)
Improving noradrenaline infusion technique.
S Genay et al.
Anaesthesia, 68(6), 647-648 (2013-05-15)

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