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Acetylcholine-d16bromide - ≥98.0%, high purity , CAS No.347841-43-4

COA

Grade & Purity:

≥98%

Cas Number: 347841-43-4
Molecular Weight: 162.31799
PubChem CID: 90472136

In stock

Item Number

A651289

Grouped product items
SKU	Size	Availability	Price	Qty
A651289-1mg	1mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$130.90
A651289-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$440.90

View related series

Ion channel (2197) Membrane Transporter/Ion Channel (1822) Metabolite (5307) nAChR (140) Neuronal Signaling (3320)

Basic Description

Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Acetylcholine-d 16 (bromide) is the deuterium labeled Acetylcholine bromide.
Storage Temp	Store at 2-8°C,Desiccated
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Acetylcholine-d 16 (bromide) is the deuterium labeled Acetylcholine bromide. In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid

Names and Identifiers

IUPAC Name	[1,1,2,2-tetradeuterio-2-(2,2,2-trideuterioacetyl)oxyethyl]-tris(trideuteriomethyl)azanium;bromide
INCHI	InChI=1S/C7H16NO2.BrH/c1-7(9)10-6-5-8(2,3)4;/h5-6H2,1-4H3;1H/q+1;/p-1/i1D3,2D3,3D3,4D3,5D2,6D2;
InChIKey	ZEHGKSPCAMLJDC-ZHEXTGARSA-M
Smiles	CC(=O)OCC[N+](C)(C)C.[Br-]
Isomeric SMILES	[2H]C([2H])([2H])C(=O)OC([2H])([2H])C([2H])([2H])[N+](C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H].[Br-]
Molecular Weight	162.31799
Reaxy-Rn	3572117
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3572117&ln=

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