Anodyne

Glyphosate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
169.07 g/mol [1]
Density1.74 (NTP, 1992) - Denser than water; will sink g/cm3 [1]
AppearanceWhite crystals [1]
OdorOdorless [1]
Melting point446 ° [1]
DecompositionWhen heated to decomposition it emits very toxic fumes of /nitrogen and phosphorus oxides/. [1]
Solubility5 to 10 mg/mL at 64 °F (NTP, 1992) [1]
-4.6 [1]
Structural Identifiers
[]
C3H8NO5[1]
2-(phosphonomethylamino)acetic acid [1]
C(C(=O)O)NCP(=O)(O)O [1]
InChI=1S/C3H8NO5P/c5-3(6)1-4-2-10(7,8)9/h4H,1-2H2,(H,5,6)(H2,7,8,9) [1]
InChIKeyXDDAORKBJWWYJS-UHFFFAOYSA-N [1]
Toxicity
[]
Human - male:
- oral: 1214 mg/kg
Human - male:
- oral: 2143 mg/kg
Human - female:
- oral: 4 gm/kg
Rat:
- oral: 4873 mg/kg
- intraperitoneal: 235 mg/kg
Mouse:
- oral: 1568 mg/kg
- intraperitoneal: 130 mg/kg
Rabbit:
- oral: 3800 mg/kg
- skin: 7940 mg/kg
Quail:
- oral: >4640 mg/kg
Rat:
- inhalation: >12200 mg/m3/4

Glyphosate

Glyphosate (also known as N-(Phosphonomethyl)glycine, Glyphosphate, N-Phosphomethylglycine, N-Phosphonomethylglycine, Pondmaster, Glyfos, Silglif, Glycine, N-(phosphonomethyl)-, Roundup Max or Folusen) is a substance of the carboxylic acid class.

Chemistry

 []

Glyphosate is a achiral mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 3496, Glyphosate. Accessed September 15, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/3496

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Glyphosate. UNII: 4632WW1X5A. Global Substance Registration System. Accessed September 15, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4632WW1X5A