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Trichlorfon (ISO)

Trichlorfon Struktur
52-68-6
CAS-Nr.
52-68-6
Bezeichnung:
Trichlorfon (ISO)
Englisch Name:
Trichlorfon
Synonyma:
DEP;TRICHLORPHON;METRIFONATE;Trichlorophon;dimethyl ester;Dipterex;TRICHLOROFON;chlorophos;DETF;Neguvon
CBNumber:
CB7472545
Summenformel:
C4H8Cl3O4P
Molgewicht:
257.44
MOL-Datei:
52-68-6.mol

Trichlorfon (ISO) Eigenschaften

Schmelzpunkt:
77-81 °C
Siedepunkt:
100°C
Dichte
1.73
Dampfdruck
2.1×10-4Pa (20 °C)
Brechungsindex
1.3439
storage temp. 
2-8°C
L?slichkeit
Freely soluble in water, very soluble in methylene chloride, freely soluble in acetone and in ethanol (96 per cent).
Aggregatzustand
solid
pka
6 (est.)
Farbe
Crystals
Wasserl?slichkeit
Slightly soluble. 1-5 g/100 mL at 21 ºC
Merck 
13,9696
BRN 
1709434
Stabilit?t:
Light Sensitive
IARC
3 (Vol. 30, Sup 7) 1987
NIST chemische Informationen
Metrifonate(52-68-6)
EPA chemische Informationen
Trichlorfon (52-68-6)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn,N
R-S?tze: 22-43-50/53
S-S?tze: 24-37-60-61-2
RIDADR  UN 3077 9/PG 3
WGK Germany  3
RTECS-Nr. TA0700000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29319090
Giftige Stoffe Daten 52-68-6(Hazardous Substances Data)
Toxizit?t LD50 in male, female rats (mg/kg): 630, 560 orally (Gaines)
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H334 Kann bei Einatmen Allergie, asthmaartige Symptome oder Atembeschwerden verursachen. Sensibilisierung der Atemwege Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P261, P285, P304+P341, P342+P311,P501
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gew?ssergef?hrdend Kategorie 1 Warnung GHS hazard pictogramssrc="/GHS09.jpg" width="20" height="20" /> P273, P391, P501
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Trichlorfon (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

WEISSE KRISTALLE.

CHEMISCHE GEFAHREN

Zersetzung beim Erhitzen und bei Kontakt mit S?uren und Basen unter Bildung giftiger Rauche. Greift viele Metalle an.

ARBEITSPLATZGRENZWERTE

TLV: (Einatembare Fraktion) 1 mg/m?(als TWA); Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); BEI vorhanden; (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).

AUFNAHMEWEGE

Aufnahme in den K?rper durch Inhalation des Aerosols, über die Haut und durch Verschlucken.

INHALATIONSGEFAHREN

Verdampfung bei 20°C vernachl?ssigbar; eine gesundheitssch?dliche Partikelkonzentration in der Luft kann jedoch bei Staubbildung schnell erreicht werden.

WIRKUNGEN BEI KURZZEITEXPOSITION

WIRKUNGEN BEI KURZZEITEXPOSITION:
M?glich sind Auswirkungen auf das Nervensystem (durch cholinesterasehemmende Wirkung) mit nachfolgenden Kr?mpfen, Atemversagen und Tod. Cholinesterasehemmer. Exposition gegenüber hohen Konzentrationen kann zum Tod führen. Die Auswirkungen treten u.U. verz?gert ein. ?rztliche Beobachtung notwendig.

WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION

Wiederholter oder andauernder Kontakt kann zu Hautsensibilisierung führen. M?glich sind Auswirkungen auf das Nervensystem. Cholinesterasehemmer. Kumulative Wirkung m?glich (s. AKUTE GEFAHREN/SYMPTOME).

LECKAGE

NICHT in die Kanalisation spülen. Verschüttetes Material in Beh?ltern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. An sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Pers?nliche Schutzausrüstung: Atemschutzger?t, A/P2-Filter für organische D?mpfe und sch?dlichen Staub.

R-S?tze Betriebsanweisung:

R22:Gesundheitssch?dlich beim Verschlucken.
R43:Sensibilisierung durch Hautkontakt m?glich.
R50/53:Sehr giftig für Wasserorganismen, kann in Gew?ssern l?ngerfristig sch?dliche Wirkungen haben.

S-S?tze Betriebsanweisung:

S24:Berührung mit der Haut vermeiden.
S37:Geeignete Schutzhandschuhe tragen.
S60:Dieses Produkt und sein Beh?lter sind als gef?hrlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S2:Darf nicht in die H?nde von Kindern gelangen.

Beschreibung

Trichlorfon is a colorless crystalline powder. It is soluble in water (120 g/L) and most organic solvents, except aliphatic hydrocarbons. Log Kow = 0.43. Trichlorfon is rapidly converted to dichlorvos by alkalis (2) and then hydrolyzed; DT50 (22 ?C) values at pH 4, 7, and 9 are 510 d, 46 h, and <30 min, respectively.

Chemische Eigenschaften

Trichlorfon is a white to pale yellow crystalline solid.

Verwenden

Trichlorfon is an irreversible organophosophate acetylcholinesterase inhibitor and the prodrug of Dichlorvos (D435950). Trichlorfon have also shown potential actions to be utilized as an effective org anophosphorus pesticide.

Definition

ChEBI: A phosphonic ester that is dimethyl phosphonate in which the hydrogen atom attched to the phosphorous is substituted by a 2,2,2-trichloro-1-hydroxyethyl group.

Indications

Metrifonate is an organophosphorous compound that is effective only in the treatment of S. haematobium. The active metabolite, dichlorvos, inactivates acetylcholinesterase and potentiates inhibitory cholinergic effects. The schistosomes are swept away from the bladder to the lungs and are trapped. Therapeutic doses produce no untoward side effects except for mild cholinergic symptoms. It is contraindicated in pregnancy, previous insecticide exposure, or with depolarizing neuromuscular blockers. Metrifonate is not available in the United States.

Antimicrobial activity

Useful activity is restricted to Schistosoma haematobium. It has little activity against other schistosomes. Although it exhibits activity against several other helminths, it is not used for their treatment.

Allgemeine Beschreibung

Chlorophos is a white crystalline solid. Soluble in water, benzene, chloroform, ether; insoluble in oils. Chlorophos is a wettable powder. Chlorophos can cause illness by inhalation, skin absorption and/or ingestion. Chlorophos is used as a pesticide.

Air & Water Reaktionen

Chlorophos decomposes at higher temperatures in water and at pH <5.5. Chlorophos is sensitive to prolonged exposure to moisture. Chlorophos is unstable in alkaline solutions.

Reaktivit?t anzeigen

Chlorophos is incompatible with alkalis. Chlorophos is corrosive to black iron and mild steel. Chlorophos is corrosive to metals. Chlorophos is subject to hydrolysis.

Health Hazard

INHALATION, INGESTION, AND SKIN ABSORPTION. Inhibits cholinesterase. Headache, depressed appetite, nausea, miosis are symptoms of light exposures. Moderate effects are peritoneal paralysis, diarrhea, salivation, lacrimation, sweating, dyspnea, substernal tightness, slow pulse, tremors, muscular cramps and ataxia. Severe symptoms are: pyrexia, cyanosis, pulmonary edema, areflexia, loss of sphincter control, paralysis, coma, heart block, shock and respiratory failure. EYES: Increases permeability of blood vessels in anterior eye. Reduces corneal sensitivity with glaucoma, abnormalities in intraocular tension or decreased visual acuity.

Brandgefahr

Combustible material: may burn but does not ignite readily. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Pharmazeutische Anwendungen

An organophosphorus compound. It is soluble in water and stable at room temperature. At higher temperatures it decomposes to the insecticide dichlorvos.

Handelsname

AEROL 1 (PESTICIDE)®; AGROFOROTOX®; ANTHON®; BAY 15922®; BAYER 15922®; BAYER L 13/59®; BILARCIL®; BOVINOX®[C]; BRITON®; BRITTEN®; CEKUFON®; CHLORAK®; CHLOROFTALM®; CICLO-SOM®; COMBOT®; COMBOT EQUINE®; DANEX®[C]; DEP®; DEPTHON®; DIMETOX®; DIPTEREX®; DIPTEREX® 50; DIPTEVU®; DITRIFON®; DYLOX®; DYLOX-METASYSTOX-R®; DYREX®; DYVON®; EQUINO-ACID®; EQUINO-AID®; FLIBOL E®; FLIEGENTELLE®; FOROTOX®; FOSCHLOR®; FOSCHLOR R®; FOSCHLOR R-50®; LEIVASOM®; LOISOL®; MASOTEN®[C]; MAZOTEN®; NEGUVON®; NEGUVON A®; PHOSCHLOR R50®; PROXOL®; RICIFON®; RITSIFON®; SATOX 20WSC®; SOLDEP®; SOTIPOX®; TRICHLORPHON FN®; TRINEX®; TUGON®; TUGON FLY BAIT®; TUGON STABLE SPRAY®; VERMICIDE BAYER 2349®; VOLFARTOL®; VOTEXIT®; WEC 50®; WOTEXIT®

Pharmakokinetik

Metrifonate is rapidly absorbed after oral administration, achieving a peak concentration in plasma within 1–2 h. It undergoes chemical transformation to dichlorvos, which is the active molecule. Dichlorvos is rapidly and extensively metabolized and excreted mainly in the urine.

Clinical Use

Urinary schistosomiasis (especially mass chemotherapy control programs)

Nebenwirkungen

Various side effects such as abdominal pain, gastrointestinal upsets and vertigo occur in many patients. As the worms release their hold of the veins in the bladder they pass through the blood system to the lungs, where they disintegrate; this may cause some of the side effects. Cholinesterase levels in the blood and on erythrocytes are depressed, but the significance of this is unknown.

Sicherheitsprofil

Poison by ingestion, inhalation, inti-aperitoneal, subcutaneous, intravenous, and intramuscular routes. Moderately toxic by skin contact. Human systemic effects: true cholinesterase. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Human mutation data reported. An eye irritant. When heated to decomposition it emits very toxic fumes of Cland POx.

m?gliche Exposition

Trichlorfon is used as an agricultural and forest insecticide.

Carcinogenicity

When rats were fed diets that contained 0, 50, 100, 200, 250, 400, 500, or 1000 ppm (equivalent to about 0.5, 12.5, 25, or 50 mg/kg/day) for 17 or 24 months, no treatment-related effects occurred in those fed 50–250 ppm . Histopathological results suggested the occurrence of mammary tumors in rats fed 400, 500, and 1000 ppm. In another study, when rats were fed diets containing 0, 50, 250, 500, or 1000 ppm (equivalent to about 2.5, 12.5, 25, or 50 mg/kg/day) trichlorfon for 24 months, no treatment-related effects other than whole-blood cholinesterase depression at 1000 ppm occurred . There was no increase in the incidence of either benign or malignant tumors, including mammary tumors.

Environmental Fate

Soil. Trichlorfon degraded in soil to dichlorvos (alkaline conditions) and desmethyl dichlorvos (Mattson et al., 1955).
Plant. In cotton leaves, the metabolites identified included dichlorvos, phosphoric acid, O-demethyl dichlorvos, O-demethyl trichlorfon, methyl phosphate and dimethyl phosphate (Bull and Ridgway, 1969). Chloral hydrate and trichloroethanol were r
Pieper and Richmond (1976) studied the persistence of trichlorfon in various foliage following an application rate of 1.13 kg/ha. Concentrations of the insecticide found at day 0 and 14 were 81.7 ppm and 7 ppb for willow foliage, 12.6 ppm and 670 ppb for
Chemical/Physical. At 100°C, trichlorfon decomposes to chloral. Decomposed by hot water at pH <5 forming dichlorvos (Worthing and Hance, 1991).

Stoffwechsel

Trichlorfon administered to mammals is rapidly metabolized and excreted almost completely in the urine within 6 h. Majormetabolites are dimethyl hydrogen phosphate, methyl dihydrogen phosphate, and conjugates of dichloroacetic acid and trichloroethanol. Trichlorfon is rapidly broken down in soil.

Versand/Shipping

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

Inkompatibilit?ten

This chemical may be characterized as an organo-phosphate or-chlorine compound. Organophosphates are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducin g agents such as hydrideds and active metals. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.Alkaline materials: lime, lime sulfur, etc. Corrosive to iron, steel and possibly to other metals.

Waste disposal

Add a combustible solvent and burn in a furnace equipped with an afterburner and an alkali scrubber.In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Trichlorfon (ISO) Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Trichlorfon (ISO) Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 223)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578
sales@hbmojin.com China 12835 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21638 55
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29885 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293
sales@sdzschem.com China 2930 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28172 58
Hebei Weibang Biotechnology Co., Ltd
+8615531157085
abby@weibangbio.com China 8816 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22963 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873
sales@chemdad.com China 39894 58
TopScience Biochemical
00852-68527855
info@itopbiochem.com China Hong Kong 902 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49374 58

52-68-6(Trichlorfon (ISO))Verwandte Suche:


  • O,O-Dimethyl-(2,2,2-trichloor-1-hydroxy-ethyl)-fosfonaat
  • O,O-Dimethyl-(2,2,2-trichlor-1-hydroxy-aethyl)phosphonat
  • o,o-dimethyl(2,2,2-tri-chloro-1-hydroxyethyl)phosphonate
  • o,o-dimethyl(2,2,2-trichloro-1-hydroxyethyl)phosponate
  • o,o-dimethyl-(2,2,2-trichloro-1-idrossi-etil)-fosfonato
  • o,o-dimethyl-1-oxy-2,2,2-trichloroethylphosphonate
  • O,O-Dimetil-(2,2,2-tricloro-1-idrossi-etil)-fosfonato
  • o,odimetil2,2,2-trichloro1hidroxietilfosfonato
  • oms800
  • Phoschlor
  • Phoschlor R.50
  • phoschlorr50
  • Phosphonic acid, (1-hydroxy-2,2,2-trichloroethyl)-, dimethyl ester
  • Phosphonic acid, (2,2,2-trichloro-1-hydroxyethyl)-, dimethyl ester
  • Phosphonicacid,(2,2,2-trichloro-1-hydroxyethyl)-,dimethylester
  • Polfoschlor
  • Proxol
  • Ricifon
  • Ritsifon
  • satox20wsc
  • Soldep
  • Sotipox
  • Thylate
  • Trametan
  • Trichloorfon
  • trichlorphene
  • Trichlorphon FN
  • trichlorphonfn
  • Trinex
  • Tugon
  • tugonflybait
  • tugonstablespray
  • vermicidebayer2349
  • Volfartol
  • Votexit
  • WEC 50
  • wec50
  • Wotexit
  • DYLOX (TM)
  • DYREX(R)
  • ((2,2,2-trichloro-1-hydroxyethyl)dimethylphosphonate)
  • DIPTEREX(R)
  • DIMETHYL (2,2,2-TRICHLORO-1-HYDROXYETHYL)-PHOSPHONATE
  • CHLOROFOS
  • BAYER L 13/57
  • -NADPH-d
  • NADPH-D
  • -Nicotinamide-adenine-dinucleotide-phosphoric Acid-d
  • -TPNH-d
  • Trichlorphon E.C.(30%)
  • Trichlorphon S.P.
  • Trichlorphon,powder (2.5%)
  • Parathion-methyl,E.C.
  • Lepidex
  • (2,2,2-Trichloro-1-hydroxyethyl)phosphonic acid dimethyl ester, Metrifonate
  • (2,2,2-Trichloro-1-hydroxyethyl)phosphonic acid dimethyl ester, Metrifonate, Trichlorfon
  • O,O-Dimethyl-1-hydroxy-2,2,2-trichloroethylphosphonate,98%
  • Dylox (TM) 1g [52-68-6]
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