100037-69-2 | Sodium 1,1'-(piperazine-1,4-diyl)diethanesulfonate 1-(4-(1-sulfoethyl)piperazin-1-yl)ethanesulfonate(3:2)

Packsize	Purity	Availability	Price	Discounted Price
10g	98%	in stock	$12.00	$8.00
100g	98%	in stock	$38.00	$27.00

Description

• Catalog Number: AA00608
• Chemical Name: Sodium 1,1'-(piperazine-1,4-diyl)diethanesulfonate 1-(4-(1-sulfoethyl)piperazin-1-yl)ethanesulfonate(3:2)
• CAS Number: 100037-69-2
• Molecular Formula: C16H33N4Na3O12S4
• Molecular Weight: 670.6821
• MDL Number: MFCD00066393
• SMILES: [O-]S(=O)(=O)CCN1CCN(CC1)CCS(=O)(=O)[O-].[O-]S(=O)(=O)CCN1CCN(CC1)CCS(=O)(=O)O.[Na+].[Na+].[Na+]

Computed Properties

• Complexity: 798
• Covalently-Bonded Unit Count: 5
• Heavy Atom Count: 39
• Hydrogen Bond Acceptor Count: 16
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 9

Upstream Synthesis Route

Sodium 1,4-piperazinediethanesulfonate (3:2) is a versatile compound commonly used in chemical synthesis as a buffering agent and a stabilizer in various reactions. Its primary role lies in maintaining the pH of the reaction environment, thus ensuring optimal conditions for the desired chemical transformations to take place. This compound is particularly valuable in organic synthesis where precise control of acidity or basicity is crucial for the success of the reaction. Additionally, Sodium 1,4-piperazinediethanesulfonate (3:2) is also employed as a chelating agent, aiding in the formation and stabilization of metal complexes in complexation reactions. Its ability to form stable complexes with metal ions makes it a valuable tool in the synthesis of coordination compounds and organometallic complexes. Moreover, this compound can also serve as a protecting group for certain functional groups in organic molecules, allowing selective reactions to occur in the presence of other reactive functionalities. Overall, the application of Sodium 1,4-piperazinediethanesulfonate (3:2) in chemical synthesis is diverse and essential for achieving efficient and controlled reactions in the laboratory.