Acephat (ISO)

Acephate Struktur
30560-19-1
CAS-Nr.
30560-19-1
Bezeichnung:
Acephat (ISO)
Englisch Name:
Acephate
Synonyma:
Acefato;Acephat;acephate (ISO) O S-dimethyl acetylphosphoramidothioate;ACEPHATE SOLUTION 100 NG/MYL IN ACETONIT RILE, PESTANAL;75sp;75 SP;ACEVOL;Ortril;kitron;LANCER
CBNumber:
CB5249028
Summenformel:
C4H10NO3PS
Molgewicht:
183.17
MOL-Datei:
30560-19-1.mol

Acephat (ISO) Eigenschaften

Schmelzpunkt:
93°C
Dichte
1.35
Dampfdruck
2.26 x 10-4 Pa (24 °C)
Flammpunkt:
2 °C
storage temp. 
APPROX 4°C
Löslichkeit
Chloroform: Soluble; DMSO: Soluble; Water: Soluble
pka
11.00±0.46(Predicted)
Aggregatzustand
solid
Wasserlöslichkeit
readily soluble
Merck 
13,32
BRN 
1936365
InChI
InChI=1S/C4H10NO3PS/c1-4(6)5-9(7,8-2)10-3/h1-3H3,(H,5,6,7)
InChIKey
YASYVMFAVPKPKE-UHFFFAOYSA-N
SMILES
P(NC(C)=O)(SC)(OC)=O
NIST chemische Informationen
Acephate(30560-19-1)
EPA chemische Informationen
Acephate (30560-19-1)

Sicherheit

Kennzeichnung gefährlicher Xn,F
R-Sätze: 22-36-20/21/22-11
S-Sätze: 2-36-36/37-16
RIDADR  UN1648 3/PG 2
WGK Germany  2
RTECS-Nr. TB4760000
HS Code  29299040
Giftige Stoffe Daten 30560-19-1(Hazardous Substances Data)
Toxizität LD50 orally in rats: 700 mg/kg (Magee, 1973)

Acephat (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

FARBLOSE KRISTALLEODER WEISSES PULVER MIT CHARAKTERISTISCHEM GERUCH.

CHEMISCHE GEFAHREN

Zersetzung beim Erhitzen unter Bildung giftiger Rauche mit Stickstoffoxiden, Phosphoroxidenund Schwefeloxiden.

ARBEITSPLATZGRENZWERTE

TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).

AUFNAHMEWEGE

Aufnahme in den Körper durch Verschlucken und durch Inhalation des Aerosols.

INHALATIONSGEFAHREN

Eine gesundheitsschädliche Partikelkonzentration in der Luft kann beim Versprühen oder Dispergieren schnell erreicht werden, vor allem als Pulver.

WIRKUNGEN BEI KURZZEITEXPOSITION

WIRKUNGEN BEI KURZZEITEXPOSITION:
Möglich sind Auswirkungen auf Nervensystem und Blut mit nachfolgender Cholinesterasehemmung. ärztliche Beobachtung notwendig. Die Auswirkungen treten u.U. verzögert ein.

LECKAGE

Verschüttetes Material in Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste sorgfältig sammeln. An sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Persönliche Schutzausrüstung: Atemschutzgerät, P2-Filter für schädliche Partikel.

R-Sätze Betriebsanweisung:

R22:Gesundheitsschädlich beim Verschlucken.
R36:Reizt die Augen.
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R11:Leichtentzündlich.

S-Sätze Betriebsanweisung:

S2:Darf nicht in die Hände von Kindern gelangen.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S16:Von Zündquellen fernhalten - Nicht rauchen.

Beschreibung

Acephate is an organophosphate foliar spray insecticide of moderate persistence with residual systemic activity. It is a contact and systemic insecticide and very effective against a large number of crop pests such as alfalfa looper, aphids, armyworms, bagworms, bean leaf beetle, bean leafroller, black grass bugs, bollworm, budworm, and cabbage looper. Acephate is a colourless to white solid organophosphate insecticide. Exposures to acephate cause poisoning to animals and humans. Acephate inhibits acetylcholine esterase (AchE), the essential nervous system enzyme, and causes characteristic organophosphate poisoning. The symptoms of toxicity include, but are not limited to, headache, nervousness, blurred vision, weakness, nausea, fatigue, stomach cramps, diarrhoea, difficulty in breathing, chest pain, sweating, pinpoint pupils, tearing, salivation, clear nasal discharge and sputum, vomiting, muscle twitching, muscle weakness, and, in severe poisoning, convulsions, respiratory depression, coma, and death. Acephate causes cholinesterase inhibition leading to overstimulation, respiratory paralysis, and death. The U.S. EPA classified acephate as Group C, meaning a possible human carcinogen, and therefore requires judicious handling and management.

Chemische Eigenschaften

Acephate is an organophosphate foliar spray insecticide of moderate persistence with residual systemic activity. It is a contact and systemic insecticide and very effective against a large number of crop pests, such as alfalfa looper, aphids, armyworms, bagworms, bean leafbeetle, bean leafroller, blackgrass bugs, bollworm, budworm, and cabbage looper.

Verwenden

Acephate is an organophosphate foliar spray insecticide of moderate persistence with residual systemic activity. It is a contact and systemic insecticide and very effective against a large number of crop pests, such as alfalfa looper, aphids, armyworms, bagworms, bean leafbeetle, bean leafroller, blackgrass bugs, bollworm, budworm, and cabbage looper.

Definition

ChEBI: A phosphoramide that is methamidophos in which one of the hydrogens is replaced by an acetyl group.

Allgemeine Beschreibung

A white solid. Used as a contact and systemic insecticide.

Air & Water Reaktionen

Soluble in water.

Reaktivität anzeigen

A thiophosphate ester. Organothiophosphates are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Health Hazard

Acephate is a colorless to white, solid organophosphate insecticide. Exposures to acephate cause poisoning to animals and humans. Acephate inhibits acetylcholine esterase (AchE), the essential nervous system enzyme, and causes characteristic organophosphate poi- soning. The symptoms of toxicity include, but are not limited to, headache, nervousness, blurred vision, weakness, nausea, fatigue, stomach cramps, diarrhea, diffi culty breathing, chest pain, sweating, pin-point pupils, tearing, salivation, clear nasal discharge and spu- tum, vomiting, muscle twitching, muscle weakness, and in severe poisonings, convulsions, respiratory depression, coma, and death. Acephate causes cholinesterase inhibition lead- ing to overstimulation, respiratory paralysis, and death.

Landwirtschaftliche Anwendung

Insecticide: Acephate is a general use contact and systemic insecticide. Not approved for use in EU countries. Actively registered in the U.S., homeowner use for lawns is discontinued except for treatment of fire ant mounds. Other indoor treatment has been discontinued. Used on green and lima beans, Brussels sprouts, cauliflower, celery, cotton, cottonseed, cranberries, head lettuce, macadamia nuts, peanuts, bell-and non-bell peppers, peppermint, spearmint, tobacco, and soybeans (Special Local Need Registration required in Mississippi and Texas only). Also used to control cockroach (spot treatment only) in residential and industrial buildings and insect control in forests, and on ornamental plants and to target armyworms, aphids, beetles, bollworms, borers, budworms, cankerworms, crickets, cutworms, fire ants, fleas, grasshoppers, leafhoppers, loopers, mealybugs, mites, moths, roaches, spiders, thirps, wasps, weevils, whiteflies, etc.

Handelsname

ACECAP SYSTEMIC INSECTICIDE IMPLANTS®; ACEFAL 75 PS®; ACEHERO®; ACEPHATE 97 EG®; ACEPHATE 75SP®; ACEPHATE PCO SP INSECTICIDE®; ACESUL®; ACE-TOX®; ACHERO®; ACIFAT®; ADDRESS®; AIMTHENE®; AMCOTHENE®; ASATAF®; ASIFY®; ATTACK®; CHEVRON RE 12420®; CLEAN CROP ACEPHATE 80 DF SEED PROTECTORANT®; DREXEL ACEPHATE 75 WSP®; DREXEL ACEPHATE PCO SP INSECTICIDE®; FATEL®; FORPHATE®, FORWARD®; KITRON®; KORANDA® (acephate + fenvelerate); LANCER®; ORCEPHATE®; ORTHENE®; ORTHENE 755®; Acephate 3 ORTHO 12420®; ORTRAN®; ORTRIL®; PACE®; PAYLOAD®; PILARTHENE®; PINPOINT®; PRECISE ACEPHATE®; RACET®; RE 12420®; SAPHATE®; 75 SP®; VALENT ORTHENE TECHNICAL®; VEGFRU TARGET®

Biologische Aktivität

Anticholinesterase insecticide that produces cholinotoxicity. Displays weak inhibition of rat acetylcholinesterase (AChE) but potently inhibits cockroach AChE.

Sicherheitsprofil

Poison by ingestion. Moderately toxic by skin contact and inhalation. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx, POx, and SOx. See also ESTERS.

mögliche Exposition

Acephate is a general use contact and systemic insecticide. Banned in the EU for use as a biocide and agricultural insecticide. Used on green- and limabeans, Brussels sprouts, cauliflower, celery, cotton, cottonseed, cranberries, head lettuce, macadamia nuts, peanuts, bell-and nonbell peppers, peppermint, spearmint, tobacco, and soybeans (Special Local Need Registration required in Mississippi and Texas only). Also used to control cockroach (spot treatment only) in residential and industrial buildings and insect control in forests, and on ornamental plants and to target armyworms, aphids, beetles, bollworms, borers, budworms, cankerworms, crickets, cutworms, fire ants, fleas, grasshoppers, leafhoppers, loopers, mealybugs, mites, moths, roaches, spiders, thirps, wasps, weevils, whiteflies, etc. banned for use in the EU.

Carcinogenicity

Acephate showed no evidence of carcinogenicity among rats given diets with 0, 5, 50, or 700 ppm (equivalent to about 0, 0.25, 2.5, and 35.0 mg/kg/ day, respectively) for 28 months .

Environmental Fate

Soil. In aerobic and anaerobic soils, methamidophos and carbon dioxide were identified as the major soil metabolites (Hartley and Kidd, 1987). The estimated half-life in soil is 3 days (Wauchope, 1988)
Plant. Acephate is quickly absorbed, translocated and transformed in pine seedlings (Werner, 1974) and cotton plants (Bull, 1979). The chemical was metabolized via cleavage of the amide bond to form methamidophos (O,S-dimethyl phosphoramidothioat
Chemical/Physical. Emits toxic fumes of phosphorus, nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987)

Stoffwechselwegen

Acephate is a systemic insecticide with a very favourable mammalian toxicity. The initial reaction of the biotransformation of acephate is by hydrolysis to the active acetylcholinesterase inlubitor methamidophos. In every case where the metabolism of acephate has been studied in biological systems, the production of methamidophos has been demonstrated; however, the amount of this presumed active metabolite varies greatly from organism to organism. In mammals, which are relatively insensitive to the insecticide, the primary route of stage I metabolism is mainly degradative via O-demethylation to give des-O-methylacephate. Further metabolism in mammals and birds leads to incorporation of the molecule into proteins, carbohydrates and lipids as well as to excretion. Conjugates have not been identified.

Versand/Shipping

UN2783 Organophosphorus pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3018 Organophosphorus pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous material

Inkompatibilitäten

May react with strong oxidizers such as chlorates, peroxides, nitrates, etc. In the presence of strong reducing agents such as hydrides, organophosphates form highly toxic and flammable phosphine gas. Contact with oxidizers can cause the release of toxic oxides of phosphorus. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water, and a salt that may be harmful. Incompatible with arsenic compounds(releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur).

Waste disposal

Alkaline hydrolysis or incineration. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Acephat (ISO) Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Acephat (ISO) Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 288)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Henan Alfa Chemical Co., Ltd
+8618339805032
alfa4@alfachem.cn China 12755 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5993 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652
info@fdachem.com China 8174 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845
sales@amoychem.com China 6387 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873
sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49390 58

30560-19-1(Acephat (ISO))Verwandte Suche:


  • acetylphosphoramidothioicacido,s-dimethylester
  • Chevron re 12,420
  • chevronorthene
  • chevronre12,420
  • ENT 27822
  • ent27822
  • N-(Methoxy(methylthio)phosphinoyl)acetamide
  • o,S-Dimethyl acetylamidothiophosphate
  • ACEVOL
  • ACEPHATE
  • acetamidophos
  • AIMTHENE
  • Orthene-755
  • ORTHO 124120
  • ortho124120
  • Ortril
  • Oxthene
  • N-Acetyl-phosphoramidothioic acid O,S-dimethyl ester
  • LUCID(R)
  • kitron
  • LANCER
  • Orthen
  • acephate (bsi,iso,ansi,esa,jmaf)
  • ACEPHATETECHNICAL
  • ASATAF
  • CEKUCEFATE
  • Ortean
  • Acephate ,orthene,Ortran,Tornado
  • ACEPHATE PESTANAL (O,S-DIMETHYL ACETYLPH
  • ACEPHATE, 1GM, NEAT
  • ACEPHATE SOLUTION
  • 75 SP
  • 75sp
  • Acetylphosphoramidothioic acid O,S-dimethyl ester
  • O,S-Dimethyl-N-acetylphosphoraminothionate
  • Acephate soluble powder
  • Phosphoramidothioic acid, acetyl-, O,S-dimethyl ester
  • Phosphoramidothioic acid, N-acetyl-, O,S-dimethyl ester
  • Phosphoramidothioicacid,acetyl-,O,S-dimethylester
  • phosphoramidothioicacid,n-acetyl-,o,s-dimethylester
  • RE 12420
  • re12420
  • ORTRAN
  • ORTHENE
  • ORTHENE(R)
  • ORTHENE(TM)
  • ortho 12420
  • O,S-DIMETHYL ACETYLPHOSPHOR-AMIDOTHIOATE
  • O,S-Dimethylacetylphosphoroamidothioate
  • O,S-DIMETHYL N-ACETYL-PHOSPHORAMIDOTHIOATE
  • Acephate E.C.
  • Acephate Solution, 100ppm
  • Aceprate
  • O,S-dimethyl-N-acethyl phosphoramidothioate
  • N-(Methoxy-methylsulfanylphosphoryl)acetamide
  • Acetylaminothiophosphonic acid O,S-dimethyl ester
  • Acetylphosphoramidothioic acid O,S-dimethyl
  • O,S-DimethylL n-Acetylphosphoramidothioate
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