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P9556

Sigma-Aldrich

N-(Phosphonomethyl)glycin

BioReagent, suitable for plant cell culture

Synonym(e):

Glyphosat

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About This Item

Lineare Formel:
(HO)2P(O)CH2NHCH2CO2H
CAS-Nummer:
1071-83-6
Molekulargewicht:
169.07
Beilstein:
2045054
EG-Nummer:
213-997-4
MDL-Nummer:
MFCD00055350
UNSPSC-Code:
10171502
PubChem Substanz-ID:
24899043
NACRES:
NA.71

Produktlinie

BioReagent

Qualitätsniveau

200

Form

powder

Methode(n)

cell culture | plant: suitable

mp (Schmelzpunkt)

230 °C (dec.) (lit.)

Anwendung(en)

agriculture

Versandbedingung

ambient

SMILES String

OC(=O)CNCP(O)(O)=O

InChI

1S/C3H8NO5P/c5-3(6)1-4-2-10(7,8)9/h4H,1-2H2,(H,5,6)(H2,7,8,9)

InChIKey

XDDAORKBJWWYJS-UHFFFAOYSA-N

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Allgemeine Beschreibung

Glyphosate (N-(phosphonomethyl)glycine) (sold commercially as Roundup) is the most widely used broad-spectrum systemic herbicide in the world. Consequently, the environmental effects of glyphosphate and its mechanism of action are an important area of active research.

Biochem./physiol. Wirkung

Glyphosate (N-[phosphonomethyl] glycine) is the herbicide form of the isopropylamine salt of glyphosate.
Glyphosphate inhibits the shikimate pathway-dependent synthesis of the aromatic amino acids tyrosine, tryptophan and phenylalanine at the growing points of plants.

Angaben zur Herstellung

Preparation and Use

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Aquatic Chronic 2 - Eye Dam. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
0000335838
SLCQ6487
SLCM2529
SLCL1740
SLCH2026

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Die Dokumentenbibliothek aufrufen

Influence of glyphosate (N-(phosphonomethyl) glycine) on performance and selected parameters in broilers
Kubena L F, et al.
Poultry Science, 60(1), 132-136 (1981)
Apoorva Ravishankar et al.
Environmental pollution (Barking, Essex : 1987), 262, 114359-114359 (2020-05-24)
Glyphosate-based herbicides, the most extensively used herbicides in the world, are available in an enormous number of commercial formulations with varying additives and adjuvants. Here, we study the effects of one such formulation, Credit41, in two genetically diverse yeast strains.
Stephen O Duke
Journal of agricultural and food chemistry, 59(11), 5835-5841 (2010-10-06)
High levels of aminomethylphosphonic acid (AMPA), the main glyphosate metabolite, have been found in glyphosate-treated, glyphosate-resistant (GR) soybean, apparently due to plant glyphosate oxidoreductase (GOX)-like activity. AMPA is mildly phytotoxic, and under some conditions the AMPA accumulating in GR soybean
Stephen O Duke et al.
Pest management science, 64(4), 319-325 (2008-02-15)
Since its commercial introduction in 1974, glyphosate [N-(phosphonomethyl)glycine] has become the dominant herbicide worldwide. There are several reasons for its success. Glyphosate is a highly effective broad-spectrum herbicide, yet it is very toxicologically and environmentally safe. Glyphosate translocates well, and
Dale L Shaner et al.
Pest management science, 68(1), 3-9 (2011-08-16)
The intensive use of glyphosate alone to manage weeds has selected populations that are glyphosate resistant. The three mechanisms of glyphosate resistance that have been elucidated are (1) target-site mutations, (2) gene amplification and (3) altered translocation due to sequestration.
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