(Aminomethyl)phosphonic acid - CAS 1066-51-9

Catalog:	BB001900
Product Name:	(Aminomethyl)phosphonic acid
CAS:	1066-51-9
Synonyms:	aminomethylphosphonic acid

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BB001900	20 g	$285	In stock

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Computed Properties

IUPAC Name:	aminomethylphosphonic acid
Description:	Aminomethanephosphonic acid is a degradation product of the herbicide glyphosate.
Molecular Weight:	111.04
Molecular Formula:	CH6NO3P
Canonical SMILES:	C(N)P(=O)(O)O
InChI:	InChI=1S/CH6NO3P/c2-1-6(3,4)5/h1-2H2,(H2,3,4,5)
InChI Key:	MGRVRXRGTBOSHW-UHFFFAOYSA-N
Boiling Point:	358 °C at 760 mmHg
Melting Point:	300 °C
Purity:	98 %
Density:	1.635 g/cm³
Appearance:	White crystals or powder
Storage:	0-6 °C
MDL:	MFCD00008105
LogP:	-0.21940

Publication Number	Title	Priority Date
EP-2960209-A1	A method for purification of a cobalt containing solution by continuous ion exchange	20140617
US-2015361524-A1	Method for Purification of a Cobalt Containing Solution by Continuous Ion Exchange	20140617
US-2015352744-A1	Methods of conferring fire retardancy to wood and fire-retardant wood products	20140604
WO-2015187414-A1	Methods of conferring fire retardancy to wood and fire-retardant wood products	20140604
WO-2015142313-A1	Printable media	20140317

PMID	Publication Date	Title	Journal
34009015	20210501	Prenatal Exposure to Glyphosate and Its Environmental Degradate, Aminomethylphosphonic Acid (AMPA), and Preterm Birth: A Nested Case-Control Study in the PROTECT Cohort (Puerto Rico)	Environmental health perspectives
33803994	20210315	Glyphosate and AMPA Induce Alterations in Expression of Genes Involved in Chromatin Architecture in Human Peripheral Blood Mononuclear Cells (In Vitro)	International journal of molecular sciences
31874349	20200201	Use of human neuroblastoma SH-SY5Y cells to evaluate glyphosate-induced effects on oxidative stress, neuronal development and cell death signaling pathways	Environment international
30605748	20190401	Effects of glyphosate and aminomethylphosphonic acid on an isogeneic model of the human blood-brain barrier	Toxicology letters
31295307	20190101	Glyphosate-based herbicides at low doses affect canonical pathways in estrogen positive and negative breast cancer cell lines	PloS one

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Related Functional Groups

Phosphorus Compounds

[115826-95-4]
Dichloro[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]palladium(II)
[60902-45-6]
n-Nonyl triphenylphosphonium bromide
[188945-44-0]
Ethyl 2-bis(2-propan-2-ylphenoxy)phosphorylacetate
[54965-29-6]
Ethyl 6-(diethylphosphono)hexanoate
[719-80-2]
Ethyl diphenylphosphinite
[16139-79-0]
Ethyl diphenylphosphono acetate

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GHS Hazard Statement:	H302 (11.11%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501
Signal Word:	Danger

Complexity:	74.9
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	111.00853005
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	3
Isotope Atom Count:	0
Monoisotopic Mass:	111.00853005
Rotatable Bond Count:	1
Topological Polar Surface Area:	83.6 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-4.7