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EDTMP: Difference between revisions

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Revision as of 18:05, 8 August 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Wiki← Previous edit Latest revision as of 18:06, 2 September 2024 edit undoHudecEmil (talk | contribs)Extended confirmed users6,115 edits degradation 
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{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 443716757 | verifiedrevid = 443718549
| ImageFile = EDTMP.png | ImageFile = EDTMP.png
| PIN={Ethane-1,2-diylbis}tetrakis(phosphonic acid)
|IUPACName=methylphosphonic acid
|OtherNames=Ethylenediamine tetra(methylene phosphonic acid), EDTMP | OtherNames=Ethylenediamine tetra(methylene phosphonic acid), EDTMP
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 14301 | ChemSpiderID = 14301
| InChI = 1/C6H20N2O12P4/c9-21(10,11)3-7(4-22(12,13)14)1-2-8(5-23(15,16)17)6-24(18,19)20/h1-6H2,(H2,9,10,11)(H2,12,13,14)(H2,15,16,17)(H2,18,19,20) | InChI = 1/C6H20N2O12P4/c9-21(10,11)3-7(4-22(12,13)14)1-2-8(5-23(15,16)17)6-24(18,19)20/h1-6H2,(H2,9,10,11)(H2,12,13,14)(H2,15,16,17)(H2,18,19,20)
Line 15: Line 16:
| CASNo_Ref = {{cascite|correct|CAS}} | CASNo_Ref = {{cascite|correct|CAS}}
| CASNo= 1429-50-1 | CASNo= 1429-50-1
| PubChem = 15025 | PubChem = 15025
| UNII_Ref = {{fdacite|correct|FDA}} | UNII_Ref = {{fdacite|correct|FDA}}
| UNII = V4CP8RSX7V | UNII = V4CP8RSX7V
| SMILES = O=P(O)(O)CN(CP(=O)(O)O)CCN(CP(=O)(O)O)CP(=O)(O)O | SMILES = O=P(O)(O)CN(CP(=O)(O)O)CCN(CP(=O)(O)O)CP(=O)(O)O
}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| Formula=C<sub>6</sub>H<sub>20</sub>N<sub>2</sub>O<sub>12</sub>P<sub>4</sub> | Formula=C<sub>6</sub>H<sub>20</sub>N<sub>2</sub>O<sub>12</sub>P<sub>4</sub>
| MolarMass | MolarMass = 436.13
| Appearance= solid | Appearance= solid
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility= limited | Solubility= limited
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
}} }}


'''EDTMP''' or '''ethylenediamine tetra(methylene phosphonic acid) ''' is a ]. It has ] and anti corrosion properties. EDTMP is the phosphonate analog of ]. '''EDTMP''' or '''ethylenediamine tetra(methylene phosphonic acid) ''' is a ]. It has ] and anti corrosion properties. EDTMP is the phosphonate analog of ].<ref name=Svara>Svara, J.; Weferling, N.; Hofmann, T. "Phosphorus Compounds, Organic," In 'Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2008. {{doi|10.1002/14356007.a19_545.pub2}}.</ref> It is classified as a nitrogenous organic polyphosphonic acid.
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==Properties== ==Properties and applications==
EDTMP is normally delivered as its sodium salt, which exhibits good solubility in water.
EDTMP is normally delivered as salts, due to the acid form has very limited solubility in water. It is a nitrogenous organic polyphosphonic acid. Its corrosion inhibition is 3-5 times better than that of inorganic ], has good chemical stability and thermal tolerance. It shows excellent scale inhibition ability under temperature 200 °C. It can dissociate into 8 positive-negative ions, thus can chelate with many metal ions to form polymer reticulation complex, to destroy the normal crystallization of calcium scale. EDTMP shows better antiscale effects to ] and ].
Used in ] as an anti] and ] agent, the corrosion inhibition of EDTMP is 3–5 times better than that of inorganic ]. It can degrade to ].<ref name="y558">{{cite journal | last=Klinger | first=J. | last2=Lang | first2=M. | last3=Sacher | first3=F. | last4=Brauch | first4=H.-J. | last5=Maier | first5=D. | last6=Worch | first6=E. | title=Formation of Glyphosate and AMPA During Ozonation of Waters Containing Ethylenediaminetetra(methylenephosphonic acid) | journal=Ozone: Science & Engineering | volume=20 | issue=2 | date=1998 | issn=0191-9512 | doi=10.1080/01919519808547279 | pages=99–110}}</ref> It shows excellent scale inhibition ability under temperature 200&nbsp;°C. It functions by chelating with many metal ions.


The anti-cancer drug ] is also derived from EDTMP.
==Applications==

* ] and cleaning agents
==References==
* ]
<references />
* ] inhibitor
* ]
** in the anti-cancer drug ]
* ] / ] retarder
* ] agent


] ]
] ]
]
]
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]
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