Name: 6,7-Dimethoxy-2-(piperazin-1-yl)quinazolin-4-amine Dihydrochloride Dihydrate
Brand: Mikromol
SKU: MM0085.08-0025

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Product Overview

Product Code

MM0085.08-0025

EP Description

Doxazosin Mesilate Impurity G as Dihydrochloride Dihydrate, Prazosin Hydrochloride Impurity C as Dihydrochloride Dihydrate, Terazosin Hydrochloride Dihydrate Impurity C as Dihydrochloride Dihydrate

USP Description

Terazosin Related Compound A as Dihydrochloride

Product Format

Neat

Molecular Formula

C14 H19 N5 O2 . 2 Cl H . 2 H2 O

Molecular Weight

398.29

API Family

Terazosin Hydrochloride Dihydrate, Prazosin Hydrochloride, Doxazosin Mesilate

Product Categories

Cardiac drugs and beta blockers, Mikromol, Impurity Reference Materials

Product Type

Impurity

Drug Type

Antihypertensives; Benign Prostatic Hypertrophy Agents

Documentation

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Product Information

Analyte Data

Analyte Name

6,7-Dimethoxy-2-(piperazin-1-yl)quinazolin-4-amine Dihydrochloride Dihydrate

Molecular Formula

C14 H19 N5 O2 . 2 Cl H . 2 H2 O

Molecular Weight

398.29

Accurate Mass

397.1284

SMILES

O.O.Cl.Cl.COc1cc2nc(nc(N)c2cc1OC)N3CCNCC3

InChI

InChI=1S/C14H19N5O2.2ClH.2H2O/c1-20-11-7-9-10(8-12(11)21-2)17-14(18-13(9)15)19-5-3-16-4-6-19;;;;/h7-8,16H,3-6H2,1-2H3,(H2,15,17,18);2*1H;2*1H2

IUPAC

6,7-dimethoxy-2-piperazin-1-ylquinazolin-4-amine;dihydrate;dihydrochloride

Product Data

Storage Temperature

+5°C

Shipping Temperature

Room Temperature

Country of Origin

GERMANY

Product Type

Impurity

Product Format

Neat

Impurity Type

Degradation product; By-product

API Family

Terazosin Hydrochloride Dihydrate; Prazosin Hydrochloride; Doxazosin Mesilate

Product citations

Why work with us?

At Mikromol, we go beyond the standard to produce high-quality, globally relevant pharmaceutical reference standards that you can trust. For more than 25 years we have delivered quality reference standards for analytical development, method validation, and stability and release testing to customers around the world.

Alongside a market-leading product range accredited to ISO 17034, the majority of our 5,000+ impurity, API and excipient reference standards are manufactured under ISO/IEC 17025 and accompanied by an extensive Certificate of Analysis.

With unparalleled depth of knowledge, decades of manufacturing experience and unrivalled scientific excellence, we work tirelessly to help you create ever better, safer medicines.

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