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Product Name:Phosphinothricine
CAS:35597-44-5
Purity:>95% by HPLC Remarks:https://bio-fermen.bocsci.com/product/phosphinothricine-cas-35597-44-5-359056.html
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| | Glufosinate-P Basic information |
| Product Name: | Glufosinate-P | | Synonyms: | Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)-, (2S)-;(S)-2-Amino-4-(hydroxymethylphosphinyl)butyric acid;(S)-4-[Hydroxy(methyl)phosphinyl]-2-aminobutyric acid;(S)-Phosphinothricin;Phosphinothricine;Glufosinate Impurity 5;L-PHOSPHINOTHRICINQ: What is
L-PHOSPHINOTHRICIN Q: What is the CAS Number of
L-PHOSPHINOTHRICIN;L-Phosphinothricin | | CAS: | 35597-44-5 | | MF: | C5H12NO4P | | MW: | 181.13 | | EINECS: | | | Product Categories: | | | Mol File: | 35597-44-5.mol |  |
| | Glufosinate-P Chemical Properties |
| Melting point | 209-210 °C | | Boiling point | 519.1±45.0 °C(Predicted) | | alpha | D25 +13.4° (c = 1 in water) | | density | 1.378±0.06 g/cm3(Predicted) | | pka | 2.22±0.10(Predicted) |
| | Glufosinate-P Usage And Synthesis |
| Chemical Properties | A 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid that has S configuration at position 2. A glutamine synthetase inhibitor, it is used (generally as the corresponding ammonium or sodium salts, known as glufosinate-P-ammonium and glufosinate-P-sodium, respectively) as a herbicide to control annual weeds and grasses. | | Definition | ChEBI: Glufosinate-P is a 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid that has S configuration at position 2. A glutamine synthetase inhibitor, it is used (generally as the corresponding ammonium or sodium salts, known as glufosinate-P-ammonium and glufosinate-P-sodium, respectively) as a herbicide to control annual weeds and grasses. It has a role as a herbicide, an EC 6.3.1.2 (glutamate--ammonia ligase) inhibitor and an agrochemical. It is an enantiomer of a (2R)-glufosinate. It is a tautomer of a glufosinate-P zwitterion. | | Biological Activity | Through oxidative stress C. elegans, racemic glufosinate-ammonium l-glufosinate-ammonium (Glufosinate-P) both mediated developmental toxicity (shortened developmental cycle, reduced body length width, promoted aging and decreased longevity), neurotoxicity (inhibited head swinging, body bending frequency acetylcholinesterase [AchE] activity) reproductive toxicity (significant reductions in number eggs offspring in vivo induced apoptosis gonadal cells). The degradation rate of L-glufosinate-ammonium was faster than that of D-glufosinate-ammonium. Based on MDA content, protein content, and antioxidant enzyme (SOD CAT) activity, Meng et al. found that L-glufosinate-ammonium could cause more severe oxidative damage than rac-glufosinate-ammonium[1-2]. | | References | [1] Xu Zhao . “Comparison of the chronic and multigenerational toxicity of racemic glufosinate and l-glufosinate to Caenorhabditis elegans at environmental concentrations.” Chemosphere 316 (2023): Article 137863.
[2] Tianyou Feng. “Comparative analysis of toxicity and metabolomic profiling of rac-glufosinate and L-glufosinate in zebrafish.” Aquatic Toxicology 261 (2023): Article 106618. |
| | Glufosinate-P Preparation Products And Raw materials |
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