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[(pentylamino)methanediyl]bis(phosphonic acid) is an organophosphorus compound characterized by its chemical formula C10H28N2O6P2. This phosphonic acid derivative features two phosphonic acid groups connected by a pentylamino group, which contributes to its unique properties and applications.

71066-29-0

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71066-29-0 Usage

Uses

Used in Corrosion Inhibition:
[(pentylamino)methanediyl]bis(phosphonic acid) is used as a corrosion inhibitor for metal surfaces, particularly those exposed to harsh environments. Its strong chelating properties allow it to form stable complexes with metal ions, effectively preventing corrosion by creating a protective layer on the metal surfaces.
Used in Water Treatment:
In the water treatment industry, [(pentylamino)methanediyl]bis(phosphonic acid) is utilized as a scale inhibitor and dispersant. Its ability to bind with metal ions helps in preventing the formation of scale, which can cause blockages and reduce the efficiency of water treatment systems.
Used in Oilfield Applications:
[(pentylamino)methanediyl]bis(phosphonic acid) is also employed in the oilfield industry, where it serves as a scale inhibitor and dispersant. This helps in maintaining the efficiency of oil extraction processes and preventing potential damage to equipment due to scale buildup.

Check Digit Verification of cas no

The CAS Registry Mumber 71066-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,6 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71066-29:
(7*7)+(6*1)+(5*0)+(4*6)+(3*6)+(2*2)+(1*9)=110
110 % 10 = 0
So 71066-29-0 is a valid CAS Registry Number.

71066-29-0SDS

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 [(pentylamino)methylene]-1,1-bisphosphonate

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:71066-29-0 SDS

71066-29-0Downstream Products

71066-29-0Relevant academic research and scientific papers

Synthesis and biological evaluation of 1-alkylaminomethyl-1,1-bisphosphonic acids against Trypanosoma cruzi and Toxoplasma gondii

Galaka, Tamila,Falcone, Bruno N.,Li, Catherine,Szajnman, Sergio H.,Moreno, Silvia N.J.,Docampo, Roberto,Rodriguez, Juan B.

, p. 3663 - 3673 (2019/07/10)

As an extension of our project aimed at the search for new chemotherapeutic agents against Chagas disease and toxoplasmosis, several 1,1-bisphosphonates were designed, synthesized and biologically evaluated against Trypanosoma cruzi and Toxoplasma gondii,

The preparation of N-substituted aminomethylidenebisphosphonates and their tetraalkyl esters via reaction of isonitriles with trialkyl phosphites and hydrogen chloride. Part 1

Goldeman, Waldemar,Kluczyński, Artur,Soroka, Miros?aw

, p. 5290 - 5292 (2012/11/13)

The reaction of isonitriles with trialkyl phosphites in the presence of hydrogen chloride gives tetraalkyl N-substituted aminomethylidenebisphosphonates via N-methylideneaminium (isonitrilium) salts. Hydrolysis or dealkylation of these tetraalkyl esters gives N-substituted aminomethylidenebisphosphonic acids in high yields.

Effects of Bisphosphonates on the Growth of Entamoeba histolytica and Plasmodium Species in Vitro and in Vivo

Ghosh, Subhash,Chan, Julian M. W.,Lea, Christopher R.,Meints, Gary A.,Lewis, Jared C.,Tovian, Zev S.,Flessner, Ryan M.,Loftus, Timothy C.,Bruchhaus, Iris,Kendrick, Howard,Croft, Simon L.,Kemp, Robert G.,Kobayashi, Seike,Nozaki, Tomoyoshi,Oldfield, Eric

, p. 175 - 187 (2007/10/03)

The effects of a series of 102 bisphosphonates on the inhibition of growth of Entamoeba histolytica and Plasmodium falciparum in vitro have been determined, and selected compounds were further investigated for their in vivo activity. Forty-seven compounds tested were active (IC50 50 ~ 4-9 μM) were nitrogen-containing bisphosphonates with relatively large aromatic side chains. Simple n-alkyl-1-hydroxy-1,1-bisphosphonates, known inhibitors of the enzyme farnesylpyrophosphate (FPP) synthase, were also active, with optimal activity being found with C9-C10 side chains. However, numerous other nitrogen-containing bisphosphonates known to be potent FPP synthase inhibitors, such as risedronate or pamidronate, had little or no activity. Several pyridine-derived bisphosphonates were quite active (IC50 ~ 10-20 μM), and this activity was shown to correlate with the basicity of the aromatic group, with activity decreasing with increasing pKa values. The activities of all compounds were tested versus a human nasopharyngeal carcinoma (KB) cell line to enable an estimate of the therapeutic index (TI). Five bisphosphonates were selected and then screened for their ability to delay the development of amebic liver abscess formation in an E. histolytica infected hamster model. Two compounds were found to decrease liver abscess formation at 10 mg/kg ip with little or no effect on normal liver mass. With P. falciparum, 35 compounds had IC50 values 50 values around 1 μM. Five compounds were again selected for in vivo investigation in a Plasmodium berghei ANKA BALB/c mouse suppressive test. The most active compound, a C9 n-alkyl side chain containing bisphosphonate, caused an 80% reduction in parasitemia with no overt toxicity. Taken together, these results show that bisphosphonates appear to be useful lead compounds for the development of novel antiamebic and antimalarial drugs.

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