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1,2-BENZENEDIPHOSPHONIC ACID (C6H4P2O6) is an aromatic diphosphonate ligand used in the synthesis of hybrid organic-inorganic frameworks, particularly in uranyl-based materials. It forms stable coordination complexes with uranium (e.g., uranyl peroxide clusters) and silver, contributing to the structural diversity of metal-organic frameworks (MOFs) and layered compounds. Its rigid phenyl backbone and dual phosphonate groups enable the formation of extended networks, as demonstrated in mixed-valent silver uranyl phosphonate frameworks, where it facilitates 2D layered architectures.

28255-47-2

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28255-47-2 Usage

Appearance

White crystalline solid

Solubility

Soluble in water

Uses

Corrosion inhibitor in industrial water treatment processes
Chelating agent in detergents and cleaning products
Manufacturing of flame retardants
Stabilizer in the production of polymers

Functional groups

Two phosphonic acid functional groups

Effectiveness

Prevents the formation of scale and rust on metal surfaces

Check Digit Verification of cas no

The CAS Registry Mumber 28255-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,5 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28255-47:
(7*2)+(6*8)+(5*2)+(4*5)+(3*5)+(2*4)+(1*7)=122
122 % 10 = 2
So 28255-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O6P2/c7-13(8,9)5-3-1-2-4-6(5)14(10,11)12/h1-4H,(H2,7,8,9)(H2,10,11,12)/p-4

28255-47-2SDS

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 (2-phosphonophenyl)phosphonic acid

1.2 Other means of identification

Product number -
Other names Benzene-1,4-diphosphonic 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:28255-47-2 SDS

28255-47-2Downstream Products

28255-47-2Relevant academic research and scientific papers

Supramolecular Assembly of Geometrically Unstable Hybrid Organic-Inorganic Uranyl Peroxide Cage Clusters and Their Transformations

Xu, Mengyu,Traustason, Hrafn,Bo, Fabrice Dal,Hickam, Sarah,Chong, Saehwa,Zhang, Lei,Oliver, Allen G.,Burns, Peter C.

, p. 12780 - 12788 (2019)

An aromatic ligand was introduced into the synthesis of a uranyl peroxide polyoxometalate formulated as K32(UO2)19(O2)26(OH)2(C6H4P2O6)4/su

The presence of mixed-valent silver in the uranyl phenylenediphosphonate framework

Bai, Ru,Chen, Lanhua,Zhang, Yugang,Chen, Long,Diwu, Juan,Wang, Xiao-Feng

, p. 6037 - 6041 (2020)

In this work, a new 2D layered silver uranyl phosphonate compound Ag01.51[AgI4(UO2)3(O3PC6H4PO3)(O3PC6H4PO3

Synthesis of o-Phenylene-bis(dibromophosphane) - Reaction Products of o-Phenylene-bis(dichlorophosphane)

Woerz, H.-J.,Quien, E.,Latscha, H. P.

, p. 1706 - 1710 (2007/10/02)

o-Phenylene-bis(dibromophosphane) (1) is prepared by reaction of P,P,P',P'-tetrakis(dimethylamino)-o-phenylenediphosphane with hydrogen bromide in ether.The reaction of o-phenylene-bis(dichlorophosphane) (2) with CH3OH in ether yields o-phenylene-bis(phos

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