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Propranolol Impurity, specifically N-Formylpropranolol, is an impurity of propranolol (CAS: 525-66-6), a medication with various therapeutic applications. It is characterized by its role as a β-adrenergic blocker, which contributes to its effectiveness in treating hypertension, angina, and arrhythmias (class II).

77252-87-0

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77252-87-0 Usage

Uses

Used in Pharmaceutical Preparations:
Propranolol Impurity is used as an ingredient in the preparation of calcium blockers and β-blockers, which are essential in managing cardiovascular conditions such as high blood pressure, angina, and irregular heartbeats.
Used in Organic Chemistry:
In the field of organic chemistry, Propranolol Impurity serves as a starting material for the synthesis of Indole and naphthalene derivatives. These compounds have potential applications in various chemical and pharmaceutical processes, making the impurity a valuable component in the development of new compounds and drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 77252-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77252-87:
(7*7)+(6*7)+(5*2)+(4*5)+(3*2)+(2*8)+(1*7)=150
150 % 10 = 0
So 77252-87-0 is a valid CAS Registry Number.

77252-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-formylpropranolol

1.2 Other means of identification

Product number -
Other names N-formylpropranolol

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:77252-87-0 SDS

77252-87-0Downstream Products

77252-87-0Relevant academic research and scientific papers

A novel type of N-formylation and related reactions of amines via cyanides and esters as formylating agents

Bao, Kai,Zhang, Weige,Bu, Xiujuan,Song, Zhichun,Zhang, Liang,Cheng, Maosheng

supporting information; experimental part, p. 5429 - 5431 (2009/03/11)

A novel N-formylation and related reactions proceed from cyanides promoted by esters. The Royal Society of Chemistry.

Photodegradation products of propranolol: The structures and pharmacological studies

Uwai, Koji,Tani, Marie,Ohtake, Yosuke,Abe, Shinya,Maruko, Akiko,Chiba, Takashi,Hamaya, Yoshiro,Ohkubo, Yasuhito,Takeshita, Mitsuhiro

, p. 357 - 365 (2007/10/03)

Recently, single-dose drug packaging systems, allowing the administration of multiple drugs in a single pill, have become popular for the convenience of the patient. The quality of drugs and an accurate measurement of their photostabilities within this system, however, have not been carefully addressed. Drugs that are unstable in light should be carefully handled to protect their potency and ensure their safety. Propranolol (1), a β-adrenergic receptor antagonist, is widely used for angina pectoris, arrhythmia, and hypertension. Due to its naphthalene skeleton, this drug may be both light unstable and a photosensitizing agent. In this study, we isolated three photodegraded products of propranolol (1): 1-naphthol (2), N-acetylpropranolol (3), and N-formylpropranolol (4). The structures of these compounds were determined by spectroscopic methods and chemical syntheses. We also examined the acute toxicities of these substances in mice and their binding to β-adrenergic receptors using rat cerebellum cortex membranes. Although the photoproducts isolated in this study did not exhibit any acute toxicity or significant binding to β-adrenergic receptors, these results serve as a warning to single-dose packaging systems, as propranolol (1) must be handled carefully to protect the compound from light-induced degradation.

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