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Guanidine, N'-[2-hydroxy-3-(1-piperidinyl)propoxy]-N,N-dimethyl-N''-phenyl-, monohydrochloride is a complex organic chemical compound primarily utilized in the pharmaceutical industry. It is characterized by its vasodilatory properties, which allow it to widen blood vessels and enhance blood flow. Guanidine,
N'-[2-hydroxy-3-(1-piperidinyl)propoxy]-N,N-dimethyl-N''-phenyl-,
monohydrochloride is particularly beneficial for the treatment of conditions such as hypertension, angina, and other cardiovascular diseases. Its potential applications also extend to improving cerebral blood flow, which could be advantageous for managing stroke and neurodegenerative diseases.

191159-93-0

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191159-93-0 Usage

Uses

Used in Pharmaceutical Industry:
Guanidine, N'-[2-hydroxy-3-(1-piperidinyl)propoxy]-N,N-dimethyl-N''-phenyl-, monohydrochloride is used as a pharmaceutical drug for its vasodilatory effects, which aid in the treatment of hypertension and angina by increasing blood flow to the affected areas.
Used in Cardiovascular Disease Treatment:
In the field of cardiology, Guanidine, N'-[2-hydroxy-3-(1-piperidinyl)propoxy]-N,N-dimethyl-N''-phenyl-, monohydrochloride is employed as a therapeutic agent for heart failure and other cardiovascular conditions. Its ability to dilate blood vessels can help alleviate symptoms and improve the overall cardiovascular health of patients.
Used in Neurological Applications:
Guanidine, N'-[2-hydroxy-3-(1-piperidinyl)propoxy]-N,N-dimethyl-N''-phenyl-, monohydrochloride may also be used in neurology to improve blood flow to the brain. This can be particularly beneficial for patients recovering from a stroke or those suffering from neurodegenerative diseases, as enhanced blood flow can support the delivery of oxygen and nutrients to the brain.
While the provided materials do not specify different industries for the uses of Guanidine, N'-[2-hydroxy-3-(1-piperidinyl)propoxy]-N,N-dimethyl-N''-phenyl-, monohydrochloride, the primary application is within the pharmaceutical and medical fields, particularly for cardiovascular and neurological treatments. Further research and development may reveal additional applications in other industries, but the current focus is on leveraging its vasodilatory properties for health-related purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 191159-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,1,5 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 191159-93:
(8*1)+(7*9)+(6*1)+(5*1)+(4*5)+(3*9)+(2*9)+(1*3)=150
150 % 10 = 0
So 191159-93-0 is a valid CAS Registry Number.

191159-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl-N'-[2-hydroxy-3-(1-piperidinyl)-propoxy]-N''-phenyl-guanidine Hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:191159-93-0 SDS

191159-93-0Upstream product

191159-93-0Downstream Products

191159-93-0Relevant academic research and scientific papers

Hydroxylamine derivatives useful for enhancing the molecular chaperon production and the preparation thereof

-

, (2008/06/13)

A method of increasing expression of a molecular chaperon by a cell and/or enhancing the activity of a molecular chaperon in cells is provided. The method comprises treating a cell that is exposed to a physiological stress which induces expression of a mo

Use of hydroxylamine derivatives, and method and preparations for increasing the tolerance of field crops against weather stresses

-

, (2008/06/13)

This invention relates to the use of hydroxylamine derivatives of general formula (I), wherein R1 represents phenyl, N-heteroaryl, S-heteroaryl or a naphthyl group any of which may be unsubstituted or substituted, an unsubstituted or substitute

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