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22664-55-7

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22664-55-7 Usage

Description

Metipranolol, also known as 3-(Propan-2-ylamino)propane-1,2-diol, is a non-cardioselective beta-blocker with a 4-acetoxy-2,3,5-trimethylphenoxy group substitution on the primary hydroxy group. It is primarily used in the management of open-angle glaucoma by lowering intraocular pressure.

Uses

Used in Ophthalmology:
Metipranolol is used as a medication for the treatment of open-angle glaucoma. It functions by reducing intraocular pressure, which helps in managing the progression of the disease and preventing further damage to the optic nerve.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, metipranolol is utilized as an active pharmaceutical ingredient (API) for the development of glaucoma treatment medications. It is the key component in the formulation of drugs like OptiPranolol, which is manufactured by Bausch & Lomb Pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 22664-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,6 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22664-55:
(7*2)+(6*2)+(5*6)+(4*6)+(3*4)+(2*5)+(1*5)=107
107 % 10 = 7
So 22664-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H27NO4/c1-10(2)18-8-15(20)9-21-16-7-11(3)17(22-14(6)19)13(5)12(16)4/h7,10,15,18,20H,8-9H2,1-6H3

22664-55-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name metipranolol

1.2 Other means of identification

Product number -
Other names methypranol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22664-55-7 SDS

22664-55-7Upstream product

22664-55-7Downstream Products

22664-55-7Relevant articles and documents

THERAPY FOR COMPLICATIONS OF DIABETES

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, (2009/07/02)

A method for enhancing glycemic control and/or insulin sensitivity in a human subject having diabetic nephropathy and/or metabolic syndrome comprises administering to the subject a selective endothelin A (ETA) receptor antagonist in a glycemic control and/or insulin sensitivity enhancing effective amount. A method for treating a complex of comorbidities in an elderly diabetic human subject comprises administering to the subject a selective ETA receptor antagonist in combination or as adjunctive therapy with at least one additional agent that is (i) other than a selective ETA receptor antagonist and (ii) effective in treatment of diabetes and/or at least one of said comorbidities other than hypertension. A therapeutic combination useful in such a method comprises a selective ETA receptor antagonist and at least one antidiabetic, anti-obesity or antidyslipidemic agent other than a selective ETA receptor antagonist.

FLUORESCENCE BASED DETECTION OF SUBSTANCES

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, (2009/09/28)

A method for the fluorescent detection of a substance, the method comprising providing particles comprising a metal or a metal oxide core, wherein one or more optionally fluorescently tagged antibodies or human specific peptide nucleic acid (PNA) oligomers for binding to a substance is/are bound, directly or indirectly, to the surface of the metal or metal oxide; contacting a substrate, which may or may not have the substance on its surface, with the particles for a time sufficient to allow the antibody/PNA oligomer to bind with the substance; removing those particles which have not bound to the substrate; if the antibodies or PNA oligomers are not fluorescently tagged, contacting the substrate with one or more fluorophores that selectively bind with the antibody and/or substance, then optionally washing the substrate to remove unbound fluorophores; and illuminating the substrate with appropriate radiation to show the fluorophores on the substrate.

Enteric coated mixture of 4-(2-hydroxy-3-isopropylamino-propoxy) indole and sodium lauryl sulphate

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, (2008/06/13)

The present invention provides a pharmaceutical composition for controlled release of 4-(2-hydroxy-3-isopropylamino-propoxy) indole in the intestinal tract, admixed with sodium lauryl sulphate, and enteric coated.

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