Dihydrogalanthamine hydrobromide

Cat. No.: HY-108723 Purity: 99.45%: Data Sheet
COA

SDS
Handling Instructions
FAQs
Technical Support

Dihydrogalanthamine hydrobromide is an acetylcholinesterase inhibitor. Dihydrogalanthamine hydrobromide can be used in research on neurological diseases such as sequelae of poliomyelitis and myasthenia gravis.

For research use only. We do not sell to patients.

Dihydrogalanthamine hydrobromide Chemical Structure

CAS No. : 69353-21-5

Size	Stock	Quantity
5 mg	In-stock	Estimated Time of Arrival: December 31
10 mg	In-stock	Estimated Time of Arrival: December 31
25 mg	In-stock	Estimated Time of Arrival: December 31
50 mg	Get quote	Estimated Time of Arrival: December 31
100 mg	Get quote
200 mg	Get quote

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This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 1 publication(s) in Google Scholar

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Biological Activity
Purity & Documentation
References
Customer Review

Description

Molecular Weight

368.27

Formula

C₁₇H₂₂BrNO₃

CAS No.

69353-21-5

Appearance

Solid

Color

White to off-white

SMILES

OC1C=C2CCN(CC3=CC=C(C4=C3C2C(C1)O4)OC)C.Br

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	6 months
	-20°C	1 month

Solvent & Solubility

In Vitro:

DMSO : 5 mg/mL (13.58 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	2.7154 mL	13.5770 mL	27.1540 mL
5 mM	0.5431 mL	2.7154 mL	5.4308 mL
10 mM	0.2715 mL	1.3577 mL	2.7154 mL

View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

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(per animal)

μL

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Calculation results:

Working solution concentration: mg/mL

Purity & Documentation

Purity: 99.45%

Select Batch:

Data Sheet (276 KB) SDS (480 KB)

COA (258 KB) HNMR (179 KB) LCMS (94 KB)

Handling Instructions (2659 KB)

References

[1]. Mroczek T. Highly efficient, selective and sensitive molecular screening of acetylcholinesterase inhibitors of natural origin by solid-phase extraction-liquid chromatography/electrospray ionisation-octopole-orthogonal acceleration time-of-flight-mass spectrometry and novel thin-layer chromatography-based bioautography. J Chromatogr A. 2009 Mar 20;1216(12):2519-28. [Content Brief]

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	2.7154 mL	13.5770 mL	27.1540 mL	67.8850 mL
	5 mM	0.5431 mL	2.7154 mL	5.4308 mL	13.5770 mL
	10 mM	0.2715 mL	1.3577 mL	2.7154 mL	6.7885 mL