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17261-34-6

17261-34-6

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17261-34-6 Usage

Uses

Iminodi(methylphosphonic Acid) is used in the preparation of new synthons for designing polyfunctional chelating agents with various coordination centers.

General Description

Iminodi(methylphosphonic acid) is an iminopolyphosphonic acid derivative. It is widely used as complex forming reagent for alkylphosphonic groups. Thermal analysis has confirmed the anhydrous state of iminodi(methylphosphonic acid).

Check Digit Verification of cas no

The CAS Registry Mumber 17261-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17261-34:
(7*1)+(6*7)+(5*2)+(4*6)+(3*1)+(2*3)+(1*4)=96
96 % 10 = 6
So 17261-34-6 is a valid CAS Registry Number.
InChI:InChI=1/C2H9NO6P2/c4-10(5,6)1-3-2-11(7,8)9/h3H,1-2H2,(H2,4,5,6)(H2,7,8,9)

17261-34-6 Well-known Company Product Price

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  • Aldrich

  • (462314)  Iminodi(methylphosphonicacid)  97%

  • 17261-34-6

  • 462314-5G

  • 759.33CNY

  • Detail

17261-34-6SDS

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 IMINO-BIS(METHYLPHOSPHONIC ACID)

1.2 Other means of identification

Product number -
Other names -

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:17261-34-6 SDS

17261-34-6Relevant articles and documents

METHOD FOR THE SYNTHESIS OF ALPHA-AMINOALKYLENEPHOSPHONIC ACID

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Page/Page column 25, (2014/02/15)

The present invention is related to a new method for the synthesis of alpha-aminoalkylenephosphonic acid or its phosphonate esters comprising the steps of forming a reaction mixture by mixing a P-O-P anhydride moiety comprising compound, having one P-atom at the oxidation state (+111) and the other P-atom at the oxidation state (+111) or (+V), an aminoalkanecarboxylic acid and an acid catalyst, wherein said reaction mixture comprises an equivalent ratio of alpha-aminoalkylene carboxylic acid to P-O-P anhydride moieties of at least 0.2, and recovering the resulting alpha-aminoalkylene phosphonic acid compound or an ester thereof from the reaction mixture.

Hydrothermal synthesis and crystal structure of two Co phosphonates containing trifunctional phosphonate anions: Co3(O 3PCH2NH2CH2PO3) 2 and Co3(O3PCH2

Turner, Adele,Jaffres, Paul-Alain,MacLcan, Elizabeth J.,Villemin, Didier,McKee, Vickie,Hix, Gary B.

, p. 1314 - 1319 (2007/10/03)

Two cobalt phosphonates containing trifunctional phosphonate anions have been synthesised and their structures solved by single crystal diffraction. Co3(O3PCH2NH2CH2PO 3)2 (3) wa

THERMAL DECOMPOSITION OF NITRILOTRIMETHYLPHOSPHONIC ACID IN AQUEOUS SOLUTIONS

Kaslina, N. A.,Polyakova, I. A.,Kessenikh, A. V.,Zhadanov, B. V.,Rudomino, M. V.,et al.

, p. 472 - 475 (2007/10/02)

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