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Carteolol Hydrochloride EP Impurity H Hydrochloride

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COA COO

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Carteolol Hydrochloride EP Impurity H Hydrochloride

Impurity

CAS Number

53371-79-2

Molecular Formula

C16H22N2O3.HCl

Product format

Neat

Molecular Weight

290.36 36.46

Storage

-20°C

Shipping

Room Temperature

API Family

Carteolol Hydrochloride

Synonyms

5-(3-(tert-butylamino)-2-hydroxypropoxy)quinolin-2(1H)-one and hydrochloride (1:1)

Iupac Name

5-[3-(tert-butylamino)-2-hydroxypropoxy]-1H-quinolin-2-one;hydrochloride

InChI

InChI=1S/C16H22N2O3.ClH/c1-16(2,3)17-9-11(19)10-21-14-6-4-5-13-12(14)7-8-15(20)18-13;/h4-8,11,17,19H,9-10H2,1-3H3,(H,18,20);1H

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COA COO

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
100mg
CE5761.17-100MG

3-4 weeks

25mg
CD5761.17-25MG

3-5 weeks

25mg
CB5761.17-25MG

4-5 weeks

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Product Type

Impurity

Our Impurity Characterized Standards portfolio comprises more than 5,000 compounds accompanied by a comprehensive CoA which can be found in 3 product categories that include a set of different analytical techniques for determining Identity and Purity.

API

We have designed a range of primary API standards manufactured according to international regulations that come with the most extensive Certificate of Analysis which includes Identity checks by several techniques.

Excipient

Excipients standards comes with a detailed Certificate of Analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.

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Synthesis

We offer tailor-made synthesis services of up to gram-quantities of materials for a wide range of pharmaceutical customers. The customer can order a specific molecule that is only synthesized on your request on the scale, with the purity and with the specification or methods you require.

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