ChemicalBook Product Catalog Organic Chemistry Phosphines N-(Carboxymethyl)-N-(phosphonomethyl)-glycine

N-(Carboxymethyl)-N-(phosphonomethyl)-glycine

N-(Carboxymethyl)-N-(phosphonomethyl)-glycine Basic information
Product Name:N-(Carboxymethyl)-N-(phosphonomethyl)-glycine
Synonyms:n-(phosphonomethyl)iminodiaceticacidhydrate;n-(carboxymethyl)-n-(phosphonomethyl)-glycine;N-(PHOSPHONOMETHYL)IMINODIACETIC ACID MONOHYDRATE;PMID;N-(PHOSPHONOMETHYL)IMINODIACETIC ACID, 9 5%;Glyphosate-IsopropylAmmonium-N-(Phosphonomethyl)IminodiaceticAcid(Pmida)98%;N-(Phosphonomethyl)IminodiaceticAcid(Pmida)98%;N-(Phosphonomethyl)diglycine
CAS:5994-61-6
MF:C5H10NO7P
MW:227.11
EINECS:227-824-5
Product Categories:Organic Building Blocks;Phosphonic/Phosphinic Acids;Phosphorus Compounds
Mol File:5994-61-6.mol
N-(Carboxymethyl)-N-(phosphonomethyl)-glycine Structure
N-(Carboxymethyl)-N-(phosphonomethyl)-glycine Chemical Properties
Melting point 215 °C (dec.)(lit.)
Boiling point 585.9±60.0 °C(Predicted)
density 1.792±0.06 g/cm3(Predicted)
vapor pressure 0Pa at 45℃
solubility Aqueous Base (Slightly), Methanol (Slightly)
form Crystalline
pka0.90±0.10(Predicted)
BRN 1795744
Stability:Hygroscopic
CAS DataBase Reference5994-61-6(CAS DataBase Reference)
EPA Substance Registry SystemPhosphonomethyliminodiacetic acid (5994-61-6)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3261 8/PG 3
WGK Germany 1
MSDS Information
ProviderLanguage
SigmaAldrich English
N-(Carboxymethyl)-N-(phosphonomethyl)-glycine Usage And Synthesis
UsesN-(Carboxymethyl)-N-(phosphonomethyl)-glycine is used in surface modification of cobalt oxide nanoparticle to overcome any toxic effect while functioning as cancer antigen carrier.
DefinitionChEBI: A tertiary amino compound that consists of iminodiacetic acid bearing an N-phosphonomethyl substituent.
General DescriptionN-(Phosphonomethyl)iminodiacetic acid hydrate is the hydrated form of N-(phosphonomethyl)iminodiacetic acid (PMIDA; H4pmida). The solubility of PMIDA in various solvents and solvent mixtures has been studied. It is the starting material for the synthesis of N-(phosphonomethyl)iminodiacetate (pmida4-), a multidentate organic ligand. PMIDA undergoes molecular oxygen oxidation in the presence of metal salts to form N-(phosphonomethyl)glycine, also known as glyphosate. H4pmida forms the structural unit of various three-dimensional inorganic-organic hybrid compounds.
N-(Carboxymethyl)-N-(phosphonomethyl)-glycine Preparation Products And Raw materials
Raw materialsIMINODIACETIC ACID DISODIUM SALT HYDRATE-->Diethylamine hydrochloride
Preparation ProductsGlyphosate-->GLYPHOSATE-N-METHYL-->Formaldehyde
Carboxymethyl starch Sodium carboxyl methylstarch N-(phosphonomethyl) iminodiacetic acid(PMIDA) Ethyl 3-aminopropanoate hydrochloride Ethyl 2-(Chlorosulfonyl)acetate Ascoric Acid Carboxymethyl cellulose GlycineMax o-Aminophenylacetic acid 4-Aminophenylacetic acid N-(Carboxymethyl)-N-(phosphonomethyl)-glycine Sodium amino-tris(methylenesulphonate) Iminodiacetic acid CARBOXYMETHYLCELLULOSE CALCIUM Iminodiacetonitrile IMINODIACETIC ACID DISODIUM SALT GLYPHOSATE-N-METHYL Citric acid
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