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[(propylimino)bis(methylene)]diphosphonic acid is a versatile chemical compound known for its potent chelating and sequestering properties. It is effective in binding and removing metal ions from solutions, making it a valuable asset in various industrial and commercial applications.

5995-27-7

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5995-27-7 Usage

Uses

Used in Water Treatment Industry:
[(propylimino)bis(methylene)]diphosphonic acid is used as a chelating agent and sequestrant for preventing scale formation and corrosion in boilers and cooling systems. Its ability to bind metal ions helps maintain the efficiency and integrity of water treatment processes.
Used in Paper and Textile Production:
In the paper and textile industries, [(propylimino)bis(methylene)]diphosphonic acid is utilized as a stabilizer and dispersing agent. This enhances the production process and contributes to the overall quality of the final products.
Used in Oil and Gas Production:
As a corrosion inhibitor, [(propylimino)bis(methylene)]diphosphonic acid plays a crucial role in the oil and gas production industry. It helps protect equipment and infrastructure from the damaging effects of corrosion, ensuring the smooth operation of these processes.
Used in Household Cleaning Products:
[(propylimino)bis(methylene)]diphosphonic acid is also a component in household cleaning products, where it contributes to their effectiveness in removing stains and dirt. Its chelating properties help to break down and remove various types of soiling, making it a valuable addition to cleaning formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 5995-27-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,9 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5995-27:
(6*5)+(5*9)+(4*9)+(3*5)+(2*2)+(1*7)=137
137 % 10 = 7
So 5995-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H15NO6P2/c1-2-3-6(4-13(7,8)9)5-14(10,11)12/h2-5H2,1H3,(H2,7,8,9)(H2,10,11,12)

5995-27-7SDS

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 1-(6-methyl-1-prop-2-enyl-4-pyrrolidin-1-yl-2-sulfanylidenepyrimidin-5-yl)ethanone

1.2 Other means of identification

Product number -
Other names Bis-<phosphono-methyl>-propyl-amin

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:5995-27-7 SDS

5995-27-7Downstream Products

5995-27-7Relevant academic research and scientific papers

Synthesis, electrochemical and classical evaluation of the antioxidant activity of three α-aminophosphonic acids: Experimental and theoretical investigation

Mehri, Mouna,Chafai, Nadjib,Ouksel, Louiza,Benbouguerra, Khalissa,Hellal, Abdelkader,Chafaa, Salah

, p. 179 - 189 (2018)

Three α-aminophosphonic acids; namely N-Ethyliminodimethylenediphosphonic acid (N-EDMPA), N-Propyliminodimethylenediphosphonic acid (N-PDMPA) and Ethylenediamine-tetrakis(methylenephosphonic acid) (EDTMP), were synthesized by the reaction of various primary amines, paraformaldehyde and phosphorous acid in acidic medium via Moedritzer-Irani reaction. The structures of the cited compounds were confirmed by UV–Vis, FT-IR, 1H NMR, 13C NMR and 31P NMR spectra. The investigated compounds were screened for their antioxidant activity by mean of the free radical scavenging activity using 1,1-Diphenyl-2-Picryl Hydrazyl (DPPH) and Cyclic Voltammetry (CV) methods. The obtained values of the 50% inhibitory concentration (IC50), show that N-PDMPA exhibit greater antioxidant activity and the order of the antioxidant activities of the studied compounds is: EDTMP N-EDMPA N-PDMPA. Furthermore, this biological activity is in good correlation with the density functional theory (DFT) calculations.

Two new supramolecular metal diphosphonates: Synthesis, characterization, crystal structure and inhibiting effects on metallic corrosion

Gholivand, Khodayar,Yaghoubi, Rouhollah,Farrokhi, Alireza,Khoddami, Shahram

, p. 23 - 30 (2016)

Two new divalent metal(II) aminodiphosphonates with layered structure, namely, Cu(H3L1)2·2H2O (1), [H4L1=methyl-N(CH2PO3H2)2] and Cd2(H2L2)4(2), [H4L2=n-propyl-N(CH2PO3H2)2] were synthesized and characterized. The Cu(II) ions in complex 1 are octahedrally coordinated by four oxygen atoms from two chelating ligands and two phosphonate oxygen atoms from two neighboring Cu(H3L1)2 units. The Cu(H3L1)2 units are interconnected by bridging phosphonate groups, forming a 2-D metal phosphonate layer. The structure of complex 2 contains two unique Cd(II) ions octahedrally-coordinated by six phosphonate oxygen atoms from four H2L2 diphosphonate anions. Corrosion inhibition performances of 1 and 2 were also compared with each other in order to study the effect of combinations of externally added Cd/H4L2 and Cu/H4L1 (1:1 ratio) on corrosion rates of carbon steel. It was found that at pH 3.0, Cd/H4L2 or Cu/H4L1 combinations do not have noticeable corrosion inhibition efficiency for carbon steel. In contrast, at pH 7.0, higher corrosion inhibition efficiency was achieved for Cd/H4L2. Physical characterizations such as scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FTIR) were applied to study the corrosion specimens and film material.

Study on the synergistic antibacterial effect of silver-carried layered zirconium alkyl-N,N-dimethylenephosphonate

Liu, Li,Liu, Changhua,Nie, Ling,Jiang, Ting,Hong, Jing,Zhang, Xiaomei,Luo, Liehong,Wang, Xiaolan

, p. 66 - 72 (2015/07/07)

A series of zirconium alkyl-N,N-dimethylenephosphonate silver-carrying (Ag-ZRDP) were successfully prepared and their potential applications as synergistic antibacterial materials were investigated. Silver nanoparticles (Ag NPs), of 30 nm in diameter, were tightly anchored onto the zirconium alkyl-N,N-dimethylenephosphonate (ZRDP), increasing the antibacterial activity of the Ag NPs due to a decrease in the extent of nanoparticle aggregation. Due to the synergistic antibacterial effect of the Ag NPs and ZRDP, the Ag-ZRDP showed a better antibacterial activity than Ag NPs and ZRDP with a minimal inhibition concentration (MIC) of 0.25 and 0.25 μg mL-1 against Escherichia coli and Staphylococcus aureus, respectively. Additionally, the Ag-ZRDP did not show obvious cytotoxicity against mammalian cells (A549 cells), even at a concentration of 256 μg mL-1. Collectively, these properties make the newly synthesized Ag-ZRDP potentially superior as disinfectants and antiseptics for various biomedical and biotechnological applications.

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