Name | glufosinate-ammonium |
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Synonyms |
Glufosinate Ammonium
2-Amino-4-(hydroxymethylphosphinyl)butyric acid ammonium salt 2-Amino-4-(hydroxymethylphosphinyl)butanoic acid, monoammonium salt DL-Phosphinothricin, monoammonium salt 2-Amino-4-(hydroxymethylphosphinyl)butanoic acid monoammonium salt 2-Amino-4-[hydroxy(methyl)phosphoryl]butanoic acid ammoniate (1:1) Glufosinate ammonium salt Ammonium (3-amino-3-carboxypropyl)methylphosphinate ammonium (2RS)-2-amino-4-(methylphosphinato)butyric acid Monoammonium 2-amino-4-(hydroxymethylphosphinyl)butanoate Ammonium 2-amino-4-(hydroxymethylphosphinyl)butyrate Basta Monoammonium 4-[hydroxy(methyl)phosphinoyl]-DL-homoalaninate 2-Amino-4-[hydroxy(methyl)phosphoryl]butanoic acid ammoniate QVYZ2PQO&1 &&(DL) Form NH4 Salt Ammonium (DL-homoalanine-4-yl)methylphosphinate Glufosinate-ammonium MFCD00055562 Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)-, ammonium salt Ammonium 2-amino-4-[hydroxy(methyl)phosphoryl]butanoate glufosinate-ammonum EINECS 278-636-5 |
Description | Glufosinate ammonium, a phosphinic acid analogue of glutamic acid, is an herbicide which is converted by plant cells into PT (L-phosphinothricin). Glufosinate ammonium exerts neurotoxic activity[1][2]. |
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Related Catalog | |
In Vitro | Glufosinate ammonium (1-100 μM; 12DIV) disrupts cell-cell adhesion in differentiated V-SVZ neural stem cells (NSCs)[2]. Glufosinate ammonium (1-100 μM; 12DIV) significantly decreases Celsr2 gene expression at 100 μM[2]. Glufosinate ammonium impairs ependymal cell capability to synthetize cilia[2]. RT-PCR[2] Cell Line: Ependymal cells Concentration: 1, 3, 10, 100 μM Incubation Time: During 12DIV (NSCs-to-ependymal cells time point) Result: Significantly decreased Celsr2 gene expression at 100 μM. |
In Vivo | Glufosinate ammonium (10-250 mg/kg; gavage; Daily; on days 6-15 of gestation) indicates maternal toxicity in the groups given 50 or 250 mg/kg in Wistar rats[3]. The Elimination of Glufosinate ammonium (oral intubation) in the blood takes place with a half-life of less than 4 hours in male and female rats[3]. |
References |
Boiling Point | 519.1ºC at 760 mmHg |
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Melting Point | 210°C |
Molecular Formula | C5H15N2O4P |
Molecular Weight | 215.18800 |
Flash Point | 100 °C |
Exact Mass | 215.10300 |
PSA | 116.09000 |
LogP | 0.24480 |
Stability | Stable. Incompatible with strong oxidizing agents. |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07, GHS08 |
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Signal Word | Danger |
Hazard Statements | H302 + H312 + H332-H360Fd-H373 |
Precautionary Statements | P201-P260-P280-P301 + P312 + P330-P308 + P313 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22 |
Safety Phrases | 53-45 |
RIDADR | 2588 |
RTECS | EK7713600 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 2931901917 |
~% 77182-82-2 |
Literature: WO2008/138088 A2, ; Page/Page column 8-9 ; |
Precursor 1 | |
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DownStream 1 | |
HS Code | 2931900090 |
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Summary | 2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0% |