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Piperidine-1-propanesulphonic acid, also known as PPSA, is a zwitterionic sulfonic acid derivative featuring a piperidine ring. It is a water-soluble chemical compound widely recognized for its buffering capacity and pH adjustment capabilities in various chemical and biological processes. PPSA's unique properties make it a valuable component in maintaining stable pH levels and ensuring the integrity of reactions in both scientific research and industrial applications.

1132-60-1

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1132-60-1 Usage

Uses

Used in Pharmaceutical Industry:
Piperidine-1-propanesulphonic acid is used as a buffering agent and pH adjuster for drug formulation. Its ability to maintain stable pH levels ensures the stability and efficacy of pharmaceutical products during manufacturing and storage.
Used in Biochemical Research:
In biochemical research, PPSA is utilized as a buffering agent for protein purification and chromatography. Its zwitterionic nature allows for effective separation and purification of proteins, contributing to the advancement of biological studies and the development of new therapeutic agents.
Used in Chemical Processes:
Piperidine-1-propanesulphonic acid is employed as a pH adjuster in various chemical processes. Its water solubility and buffering capacity make it suitable for preparing aqueous solutions and controlling the pH of chemical reactions, thereby preventing deviations in acidity or alkalinity that could affect the outcome of the process.

Check Digit Verification of cas no

The CAS Registry Mumber 1132-60-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1132-60:
(6*1)+(5*1)+(4*3)+(3*2)+(2*6)+(1*0)=41
41 % 10 = 1
So 1132-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO3S/c10-13(11,12)8-4-7-9-5-2-1-3-6-9/h1-8H2,(H,10,11,12)

1132-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-piperidin-1-ylpropane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names 3-<1-Piperidino>-propan-1-sulfonat

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:1132-60-1 SDS

1132-60-1Downstream Products

1132-60-1Relevant academic research and scientific papers

Method for synthesizing azelaic acid monomethyl ester by catalyzing epoxy methyl oleate through ionic liquid

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Paragraph 0029-0031, (2020/12/30)

The invention relates to a method for synthesizing azelaic acid monomethyl ester by catalyzing epoxy methyl oleate with ionic liquid, which comprises the following steps: dissolving 1-(3-sulfonic acid) propyl piperidine dodecaphosphomolybdic acid ionic liquid and a certain amount of hydrogen peroxide by using a derivative epoxy methyl oleate of biodiesel as a raw material, dropwisely adding epoxymethyl oleate and a hydrogen peroxide solution, controlling the temperature, and fully stirring, after the reaction is finished, and arranging an oil layer on an upper surface, wherein an aqueous solution is dark green, obvious in layering and easy to separate; and drying the separated oily substance, carrying out high-vacuum rectification, and collecting the distillate at the temperature of 210-220 DEG C and the vacuum degree of 6-10mmHg to obtain a azelaic acid monomethyl ester finished product with the mass fraction of more than 99.0%. The method has the characteristics of simple process, no addition of other solvents and phase transfer catalysts, environment-friendly oxidation mode, no pollution and high added value of the product. The method has high reaction yield, can obtain a largeamount of high-purity azelaic acid monomethyl ester, and is easy for industrial application.

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