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5625-56-9

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5625-56-9 Usage

Description

1,4-Piperazinedipropanesulfonic acid, also known as PIPPS, is a non-metal complexing, zwitterionic buffer with mixed-mode dissociation constants of pKa1 = 3.73 and pKa2 = 7.96 (100 mM, 25°C). PIPPS has no interference at wavelengths longer than 240 nm, making it suitable for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
1,4-Piperazinedipropanesulfonic acid is used as a buffer for maintaining stable pH levels in pharmaceutical formulations. Its mixed-mode dissociation constants allow for effective buffering over a wide pH range, ensuring the stability and efficacy of the drug.
Used in Biotechnology Research:
In biotechnology research, 1,4-Piperazinedipropanesulfonic acid is used as a buffer in various biochemical assays and experiments. Its non-metal complexing property and lack of interference at wavelengths longer than 240 nm make it an ideal choice for experiments involving sensitive detection methods.
Used in Chemical Analysis:
1,4-Piperazinedipropanesulfonic acid is used as a buffer in chemical analysis to maintain a consistent pH environment during the analysis process. This ensures accurate and reliable results, particularly in applications where pH stability is crucial.
Used in Environmental Science:
In environmental science, 1,4-Piperazinedipropanesulfonic acid is used as a buffer to study the effects of pH on various environmental samples, such as soil, water, and air. Its ability to maintain a stable pH environment allows for a better understanding of the impact of pH on environmental processes and the organisms living within these systems.
Used in Material Science:
1,4-Piperazinedipropanesulfonic acid is used as a buffer in the synthesis and processing of certain materials, such as polymers and nanoparticles. Its buffering capacity helps maintain a stable pH during the synthesis process, which can be crucial for the formation and properties of the final material.

Check Digit Verification of cas no

The CAS Registry Mumber 5625-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5625-56:
(6*5)+(5*6)+(4*2)+(3*5)+(2*5)+(1*6)=99
99 % 10 = 9
So 5625-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H22N2O6S2/c13-19(14,15)9-1-3-11-5-7-12(8-6-11)4-2-10-20(16,17)18/h1-10H2,(H,13,14,15)(H,16,17,18)

5625-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(3-sulfopropyl)piperazin-1-yl]propane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names IN1146

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:5625-56-9 SDS

5625-56-9Downstream Products

5625-56-9Relevant articles and documents

Novel bi-SO3H-functionalized ionic liquids based on piperazinium: Highly efficient and recyclable catalysts for the synthesis of β-acetamido ketones

Wang, Yuanyuan,Zhou, Junlong,Liu, Kun,Dai, Liyi

, p. 195 - 201 (2013/02/22)

A series of novel bi-SO3H-functionalized ionic liquids were synthesized and acted as catalysts for the synthesis of β-acetamido ketones. Compared with traditional single-SO3H-functionalized ionic liquids, less amount of catalysts, higher yields and shorter reaction time are the key features of this methodology. Hammett function values and the minimum-energy geometries of bi-SO3H-functionalized ILs were calculated and the results revealed that the acidities and catalytic activities of ILs in synthesis of β-acetamido ketones were influenced by their structures. The IL [(PS)2pi][OTf]2 with the shortest HO bond distance had the strongest acidity and the highest catalytic activity.

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