Chemical Name: 2-(2,6-Dimethoxyphenoxyethyl)aminomethyl-1,4-benzodioxane hydrochloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
α1A-adrenergic selective antagonist. Also available as part of the α1-Adrenoceptor Tocriset™.
Technical Data
M. Wt
381.86
Formula
C19H23NO5.HCl
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
2170-58-3
PubChem ID
11957505
InChI Key
KAHMEWANVDFFCQ-UHFFFAOYSA-N
Smiles
Cl.COC1=CC=CC(OC)=C1OCCNCC1COC2=C(O1)C=CC=C2
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
water
19.09
50
Preparing Stock Solutions
The following data is based on the product molecular weight 381.86. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
2.62 mL
13.09 mL
26.19 mL
5 mM
0.52 mL
2.62 mL
5.24 mL
10 mM
0.26 mL
1.31 mL
2.62 mL
50 mM
0.05 mL
0.26 mL
0.52 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Greenet al (1969) The synthesis and pharmacological properties of a series of 2-substituted aminomethyl-1,4-benzodioxanes. J.Med.Chem. 12 326 PMID: 5791620
Heibleet al (1995) α and β-adrenoceptors: from the gene to the clinic. 1. Molecular biology and adrenoceptor subclassification. J.Med.Chem. 38 3415 PMID: 7658428
Morrow and Creese
(1986) Characterisation of α1-adrenergic receptor subtypes in rat brain: a re-evaluation of 3H-WB 4101 and 3H-prazosin binding. Mol.Pharmacol. 29 321 PMID: 3010073