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(1-aminopropane-1,3-diyl)bis(phosphonic acid), also known as bisphosphonic acid, is a chemical compound with the molecular formula C3H11NO6P2. It is a phosphonic acid derivative, which means it contains a phosphorus atom bonded to four oxygen atoms and a carbon atom. (1-aminopropane-1,3-diyl)bis(phosphonic acid) has diverse applications and plays a crucial role in various industries.

79566-02-2

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79566-02-2 Usage

Uses

Used in Pharmaceutical Industry:
(1-aminopropane-1,3-diyl)bis(phosphonic acid) is used as a treatment for bone disorders such as osteoporosis and Paget's disease. It functions by inhibiting the activity of osteoclasts, which are cells responsible for breaking down bone tissue, thereby helping to maintain bone strength and density.
Used in Food and Beverage Industry:
(1-aminopropane-1,3-diyl)bis(phosphonic acid) is used as a chelating agent to prevent the formation of scale and deposits in water systems. This helps to maintain the efficiency and longevity of equipment and管道 systems used in the food and beverage industry, ensuring the quality and safety of the products being produced.

Check Digit Verification of cas no

The CAS Registry Mumber 79566-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,6 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79566-02:
(7*7)+(6*9)+(5*5)+(4*6)+(3*6)+(2*0)+(1*2)=172
172 % 10 = 2
So 79566-02-2 is a valid CAS Registry Number.

79566-02-2SDS

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 (1-amino-3-phosphonopropyl)phosphonic acid

1.2 Other means of identification

Product number -
Other names Amino Trimethylene Phosphonic Acid

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:79566-02-2 SDS

79566-02-2Upstream product

79566-02-2Downstream Products

79566-02-2Relevant academic research and scientific papers

A general approach to enantiomeric γ-aminophosphonic acids using chiral sulfinimine methodology

Lyzwa, Piotr,Mikolajczyk, Marian

scheme or table, p. 594 - 598 (2012/01/05)

A new approach to asymmetric synthesis of γ-aminophosphonic acids is described. It involves the diastereoselective addition of various carbon and phosphorus nucleophiles to enantiopure (+)-(S)-N-[(3-diethoxyphosphoryl) propylidene]-p-toluenesulfinamide an

1-Aminoalkanediphosphonic acids. Synthesis and acidic properties

Kudzin, Zbigniew H.,Kotynski, Andrzej,Andrijewski, Grzegorz

, p. 199 - 206 (2007/10/02)

The syntheses of 1-aminoalkane-1,n-diphosphonic acids (n=2-4) by the thioureidoalkanephosphonate method are described.The acidities of these amino acids were determined potentiometrically.Key words: Phosphorus; Phosphonic acid; Aminoalkanephosphonic acids

AMINODIPHOSPHONSAEUREN UND DIAMINODIPHOSPHONSAEUREN - SYNTHESE UND TRANSAMINIERUNGSVERHALTEN

Issleib, K.,Doepfer, K.-P.,Balszuweit, A.

, p. 171 - 178 (2007/10/02)

ω-Phosphonocarbonyl compounds and dicarbonylcompounds react with benzhydrylamine to the corresponding Schiff bases.The latter add diethylphosphite under formation of N-benzhydryl-alkyl-tetraalkyl-phosphonates.Acidolysis with concentrated hydrobromic acid and following treatment with epoxide or ion exchanger gives the title compounds in high yields.The bahavior of aminophosphonic acids under transamination conditions against different substrates and with variable metal ions as catalysts has been investigated.

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