Name | Glufosinate ammonium |
Synonyms | finale hoe00661 finale14sl dl-phosphinothricin glufosinate-ammonium Glufosinate ammonium Glufodinate ammonium dl-phosphinothricinammonium DL-Phosphinothricin ammonium salt FREE SAMPLE NCV GLUFOSINATE AMMONIUM ammonium 2-amino-4(hydroxymethylphosphinyl)butanoate Ammonium 2-amino-4(hydroxymethylphosphinyl)butanoate ammonium 2-amino-4-[hydroxy(methyl)phosphoryl]butanoate 2-amino-4-(hydroxymethylphosphinyl)butyric acid ammonium salt 2-Amino-4-(hydroxymethylphosphinyl)butyric acid ammonium salt 2-amino-4-(hydroxymethylphosphinyl)butanoicacidmonoammoniumsalt |
CAS | 77182-82-2 |
EINECS | 278-636-5 |
InChI | InChI=1/C5H12NO4P.H3N/c1-11(9,10)3-2-4(6)5(7)8;/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10);1H3 |
InChIKey | ZBMRKNMTMPPMMK-UHFFFAOYSA-N |
Molecular Formula | C5H18N3O4P |
Molar Mass | 215.19 |
Density | 1.4 g/cm3 |
Melting Point | 210°C |
Boling Point | 519℃ |
Flash Point | 100°C |
Water Solubility | Soluble in water |
Solubility | Low solubility in common organic solvents and greater solubility in water. The solubility in water is 1370g/L(22 ℃). |
Vapor Presure | 3.61E-12mmHg at 25°C |
Appearance | Crystalline solid |
Color | White to Beige |
Merck | 13,7425 |
BRN | 8163399 |
pKa | 9.15[at 20 ℃] |
Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
Stability | Stable. Incompatible with strong oxidizing agents. |
MDL | MFCD00055562 |
Physical and Chemical Properties | Melting Point: 210°C |
Use | For the control of annual and perennial dicotyledonous and gramineous weeds in orchards, nurseries, non-cultivated land, potato fields, etc. |
Risk Codes | R22 - Harmful if swallowed R48/20/22 - R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R63 - Possible risk of harm to the unborn child R60 - May impair fertility |
Safety Description | S53 - Avoid exposure - obtain special instructions before use. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S24/25 - Avoid contact with skin and eyes. |
UN IDs | 2588 |
WGK Germany | 1 |
RTECS | EK7713600 |
HS Code | 29319019 |
Hazard Class | 6.1(b) |
Packing Group | III |
Toxicity | LD50 in male, female mice, male, female rats (mg/kg): 431, 416, 2000, 1620 orally (Langelüddeke) |
LogP | -4.01 at 25℃ |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
organophosphorus herbicide | glufosinate, also known as glufosinate, is a non-selective foliar-sprayed organophosphorus herbicide, it was first synthesized and developed by the Federal Republic of Germany Hoechst chemical company in 1976. The herbicidal action mechanism of Glufosinate is through the absorption of the leaves, with partial absorption, which can be transferred from the base of the leaves to the end, and less to other parts of the plant, no harm to undiscovered shoots and seeds. Ammonium metabolism in plants is disturbed in the short term after application, and strong cytotoxic ammonium ions accumulate in plants; The plants are poisoned and die. At the same time, photosynthesis was also severely inhibited, and the damaged plants were yellow and white after losing green, and began to die after 2~5 days. Loss of activity after contact with soil, only suitable for post-shoot spray. This information was edited by chemobook Yao Yao (2015-08-04). Application: Glufosinate is mainly used in orchards, nurseries, potato fields, nurseries, forests, ranches, ornamental shrubs, and non-cultivated field, to control annual and perennial Gramineae weeds, such as pinia, Wild Oats, malang, Humulus scandens, settail grass, Kentucky bluegrass, creeping grass, dog tooth root, shear, Reed, Festuca and so on. It can also control the broad-leaved weeds such as Chenopodium album, amaranth, Polygonum, chestnut, Solanum nigrum, purslane, pig, Sonchus, Thistle, Rosette, dandelion, etc, it also has a certain effect on the grass and the pteridophytes. When the Broad-leaved grass is sprayed on the weed population at a dose of 0.7-1.2/ha in the initial period of vigorous growth and the initial period of tillering of grass weeds, the control period is 4-6 weeks, if necessary, the drug can be administered again, which can significantly prolong the validity period. Potato field should be applied before Bud, It can also be sprayed before harvesting to kill the ground residues for harvesting. To control ferns, the dosage of 1.5~2kg per hectare. It is usually used alone, and sometimes it can be mixed with simazine, trichlorone or 2me4 chloride. FIG. 1 shows the chemical structural formula of glufosinate. |
toxicity | Acute oral LD50 was 2000mg/kg in male rats and 1620mg/kg in female rats; male mice acute oral LD50431mg/kg, female mice were 416mg/kg; Dogs acute oral LD50200 ~ 400mg/kg. Acute percutaneous LD50>2000mg/kg in male rats and 4000mg/kg in female rats. No teratogenic, carcinogenic effect. Rainbow trout lc50320 mg/L (96H). |
Use | organophosphate herbicide, glutamine synthesis inhibitor, non-selective contact herbicide. It has a certain role in the role of suction, can be used for the Orchard, yeast, non-cultivated land, can also be used for potato to control the annual or perennial dicotyledons and grass weeds and Cyperus, such as rat tail, horse, Tang, settail, wild wheat, wild corn, dactylit, Festuca arundinacea, curved grass, villous grass, ryegrass, Reed, Poa pratensis, wild oat, Brome, pig, baomai grass, wild sesame, solanum nigrum, flocks, creeping grass, shear, grass grass, field do not forget grass, dog tooth root, reverse branch amaranth, etc. The amount of use varies according to crops and weeds, and 1 ~ 2kg or more per hectare is used, such as the control of rubs and pteridophytes in forest and alpine pasture. The dosage was 1.5~20kg/hm2. It is used to control annual and perennial dicotyledonous and Gramineae weeds in orchards, nurseries, non-cultivated land, potato fields and so on, such as rat-tail damnique, Malang, bighead, wild barley, Lolium multiflorum, dog-tail grass, kenaf, wild wheat, wild corn, perennial grass weeds and Cyperus, such as: duck sprouts, curved grass, Festuca, and so on. |
production method | O,O-diethyl methyl phosphonic acid is reacted with dibromoethane, brCH2CH2P (O)(OC2H5)CH3 was obtained by heating at 80 ℃ for 2H, and then (C2H5O2C)2CNa(NHCOCH3) was reacted at 85 ℃ to obtain (C2H5O2C)2C(NHCOCH3)CH2CH2P(O). (OC2H5)CH3 was refluxed with hydrochloric acid, and the resulting compound was reacted with 28% ammonium hydroxide at 60-70 ° C. For 8H to obtain glufosinate. In addition, glufosinate synthesis and high-pressure catalytic synthesis, low-temperature directional synthesis method, the use of the stroeckel reaction and micheresis plus, etc. See pesticides, Issue 9, 2002. |
category | pesticide |
toxicity grade | high toxicity |
Acute toxicity | oral-rat LD50: 1620 mg/kg; Oral-mouse LD50: 416 mg/kg |
flammability hazard characteristics | flammability; Toxic nitrogen oxide and phosphorus oxide fumes from combustion |
storage and transportation characteristics | warehouse ventilation and low temperature drying |
fire extinguishing agent | dry powder, foam, sand, carbon dioxide, water mist |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |