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Glufosinate-P

CAS No.
35597-44-5
Chemical Name:
Glufosinate-P
Synonyms
L-Glufosinate;L-Glufosinate ammonium;L-Phosphinothricin;L-Glufosite;Glufosinate-P;Phosphinothricine;(S)-Phosphinothricin;Glufosinate Impurity 5;(S)-2-Amino-4-(hydroxymethylphosphinyl)butyric acid;(S)-4-[Hydroxy(methyl)phosphinyl]-2-aminobutyric acid
CBNumber:
CB81212354
Molecular Formula:
C5H12NO4P
Molecular Weight:
181.13
MDL Number:
MOL File:
35597-44-5.mol
MSDS File:
SDS
Last updated:2023-11-23 09:28:51

Glufosinate-P 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)
FDA UNII 72P470U27C

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H302-H331
Precautionary statements  P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P311-P321-P403+P233-P405-P501

Glufosinate-P Chemical Properties,Uses,Production

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.

73777-49-8
35597-44-5
Synthesis of Glufosinate-P from L-glufosinate hydrochloride

Glufosinate-P Preparation Products And Raw materials

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35597-44-5(Glufosinate-P)Related Search:

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 L-Glufosinate L-Glufosinate ammonium (2S)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Glufosinate-P L-Glufosite 35597-44-5