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Biguanide hydrochloride is a class of oral antidiabetic drugs primarily used for the treatment of type 2 diabetes. It functions by reducing hepatic glucose production, making it an effective medication in managing blood sugar levels.

4761-93-7

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4761-93-7 Usage

Uses

Used in Pharmaceutical Industry:
Biguanide hydrochloride is used as an oral antidiabetic drug for the treatment of type 2 diabetes. It helps in reducing hepatic glucose production, thereby effectively managing blood sugar levels in patients.
Additionally, Biguanide hydrochloride is often used in combination therapy with secretagogues to enhance its therapeutic effects and improve glycemic control in patients with type 2 diabetes. This combination approach allows for better management of the condition and may help in reducing the risk of complications associated with diabetes.

Check Digit Verification of cas no

The CAS Registry Mumber 4761-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,6 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4761-93:
(6*4)+(5*7)+(4*6)+(3*1)+(2*9)+(1*3)=107
107 % 10 = 7
So 4761-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C2H7N5.ClH/c3-1(4)7-2(5)6;/h(H7,3,4,5,6,7);1H

4761-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Biguanide hydrochloride

1.2 Other means of identification

Product number -
Other names Biguanide monohydrochloride

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:4761-93-7 SDS

4761-93-7Relevant academic research and scientific papers

Development of a green and sustainable manufacturing process for gefapixant citrate (MK-7264) Part 3: Development of a one-pot formylation-cyclization sequence to the diaminopyrimidine core

Basu, Kallol,Lehnherr, Dan,Martin, Gary E.,Desmond, Richard A.,Lam, Yu-Hong,Peng, Feng,Chung, John Y.L.,Arvary, Rebecca A.,Zompa, Michael A.,Zhang, Si-Wei,Liu, Jinchu,Dance, Zachary E.X.,Larpent, Patrick,Cohen, Ryan D.,Guzman, Francisco J.,Rogus, Nicholas J.,Di Maso, Michael J.,Ren, Hong,Maloney, Kevin M.

, p. 2462 - 2477 (2020)

The development of a safe, robust, and efficient manufacturing route for the synthesis of diaminopyrimidine 1, a key intermediate to gefapixant citrate (MK-7264), is described. A full mechanistic understanding of the cyclization step in the presence of guanidine was established by performing isotopic labeling experiments and identification of impurities. Guided by the mechanistic understanding, further attempts to modify the cyclization reaction by employing additives to reduce the triazine (9) formation and guanidine loading will also be presented. This newly developed method delivered compound 1 in 88-94% yield on a commercial scale and addressed the shortcomings of the early synthetic route including high PMI, low atom economy, long cycle-time, and multiple purifications to achieve the desired quality.

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

Method of making 1-(alkoxyphenyl)-5-(phenyl)biguanide compounds which are useful as agricultural fungicides

-

, (2008/06/13)

The present invention provides an improved method of making 1-(alkoxyphenyl)-5-(phenyl)biguanide compounds which are useful as agricultural fungicides, having the formula: STR1 where R is alkyl, linear of branched, having from 1-14 carbon atoms; and acid addition salts thereof. The method comprises the steps of (a) alkylating a nitrophenol with a suitable alkyl halide in a reaction solvent to form an alkoxynitrobenzene intermediate, (b) reducing the nitro group of the itermediate in situ by catalytic hydrogenation to form an alkoxyaniline, and (c) condensing the alkoxyaniline with phenyldicyandiamide to form the desired biguanide as the acid addition salt. The invention also includes a novel isolation and purification procedure for obtaining purified biguanide acid addition salts and purified free biguanide base.

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