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Parathion (ISO) Produkt Beschreibung

Parathion Struktur
56-38-2
CAS-Nr.
56-38-2
Bezeichnung:
Parathion (ISO)
Englisch Name:
Parathion
Synonyma:
AAT;1605;AATP;b404;DNTP;e605;Aralo;B 404;E 605;e605f
CBNumber:
CB4153452
Summenformel:
C10H14NO5PS
Molgewicht:
291.26
MOL-Datei:
56-38-2.mol

Parathion (ISO) Eigenschaften

Schmelzpunkt:
6.1°C
Siedepunkt:
375°C
Dichte
1.26
Dampfdruck
0.470 at 20 °C, 0.942 at 25 °C, 1.84 at 30 °C, 3.53 at 35 °C, 6.62 at 40 °C, 12.18 at 45 °C (gassaturation method, Spencer et al., 1979)
Brechungsindex
nD25 1.5370
Flammpunkt:
120 °C
storage temp. 
APPROX 4°C
Löslichkeit
2,900 and 2,700 g/kg in petroleum ether and heptane, respectively (Williams, 1951)
Aggregatzustand
liquid
Wasserlöslichkeit
Slightly soluble
Merck 
13,7105
BRN 
8912188
Henry's Law Constant
8.56 at 25 °C (wetted-wall column, Fendinger and Glotfelty, 1990)
Expositionsgrenzwerte
NIOSH REL: TWA 0.05 mg/m3, IDLH 10 mg/m3; OSHA PEL: TWA 0.1 mg/m3.
CAS Datenbank
56-38-2(CAS DataBase Reference)
NIST chemische Informationen
Ethyl parathion (o,o-diethyl-o-p-nitrophenylthiophosphate)(56-38-2)
EPA chemische Informationen
Phosphorothioic acid, O,O-diethyl O-(4-nitrophenyl) ester(56-38-2)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T+;N,N,T+,Xn,F
R-Sätze: 24-26/28-48/25-50/53-67-65-38-11
S-Sätze: 28-36/37-45-60-61-62-16
RIDADR  UN 3278
WGK Germany  3
RTECS-Nr. TF4550000
HazardClass  6.1(a)
PackingGroup  I
HS Code  29201100
Giftige Stoffe Daten 56-38-2(Hazardous Substances Data)
Toxizität LD50 in female, male rats (mg/kg): 3.6, 13 orally; 6.8, 21 dermally (Gaines)
Bildanzeige (GHS)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H225 Flüssigkeit und Dampf leicht entzündbar. Entzündbare Flüssigkeiten Kategorie 2 Achtung P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H304 Kann bei Verschlucken und Eindringen in die Atemwege tödlich sein. Aspirationsgefahr Kategorie 1 Achtung
H311 Giftig bei Hautkontakt. Akute Toxizität dermal Kategorie 3 Achtung P280, P302+P352, P312, P322, P361,P363, P405, P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H336 Kann Schläfrigkeit und Benommenheit verursachen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Schläfrigkeit und Benommenheit) Warnung P261, P271, P304+P340, P312,P403+P233, P405, P501
H372 Schädigt bei Hautkontakt und Verschlucken die Organe bei längerer oder wiederholter Exposition. Spezifische Zielorgan-Toxizität (wiederholte Exposition) Kategorie 1 Achtung P260, P264, P270, P314, P501
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 1 Warnung P273, P391, P501
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P260 Dampf/Aerosol/Nebel nicht einatmen.
P273 Freisetzung in die Umwelt vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P284 Atemschutz tragen.
P331 KEIN Erbrechen herbeiführen.
P391 Verschüttete Mengen aufnehmen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P403+P233 An einem gut belüfteten Ort aufbewahren. Behälter dicht verschlossen halten.
P403+P235 An einem gut belüfteten Ort aufbewahren. Kühl halten.

Parathion (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

HELLGELBE BIS BRAUNE (TECHNISCHES PRODUKT) FLüSSIGKEIT MIT CHARAKTERISTISCHEM GERUCH.

CHEMISCHE GEFAHREN

Zersetzung beim Erhitzen über 200 °C unter Bildung giftiger Gase mit Kohlenmonoxid, Stickstoffoxiden, Phosphoroxiden und Schwefeloxiden. Reagiert mit starken Oxidationsmitteln. Greift einige Kunststoff-, Gummi- und Beschichtungsarten an.

ARBEITSPLATZGRENZWERTE

TLV: (Einatembare Fraktion und Dampf) 0.05 mg/m? Hautresorption; Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); BEI vorhanden; (ACGIH 2005).
MAK: 0.1 mg/m?(Einatembare Fraktion); Spitzenbegrenzung: überschreitungsfaktor II(8); Hautresorption; Schwangerschaft: Gruppe D; (DFG 2005).

AUFNAHMEWEGE

Aufnahme in den Körper durch Inhalation des Aerosols, über die Haut, durch Verschlucken und über die Augen.

INHALATIONSGEFAHREN

Verdampfung bei 20 °C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch beim Versprühen schnell erreicht werden.

WIRKUNGEN BEI KURZZEITEXPOSITION

WIRKUNGEN BEI KURZZEITEXPOSITION:
Möglich sind Auswirkungen auf das Nervensystem. Führt zu Krämpfen, Atemversagen, Muskelschwäche. Cholinesterasehemmer. Exposition kann zum Tode führen. Die Auswirkungen treten u.U. verzögert ein. ärztliche Beobachtung notwendig.

WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION

Cholinesterasehemmer. Kumulative Wirkung möglich, s. AKUTE GEFAHREN/SYMPTOME.

LECKAGE

Gefahrenbereich verlassen! Fachmann zu Rate ziehen! Ausgelaufene Flüssigkeit möglichst in abdichtbaren Behältern sammeln. Reste mit basischem Stoff behandeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Persönliche Schutzausrüstung: Chemikalienschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.

R-Sätze Betriebsanweisung:

R24:Giftig bei Berührung mit der Haut.
R26/28:Sehr giftig beim Einatmen und Verschlucken.
R48/25:Giftig: Gefahr ernster Gesundheitsschäden bei längerer Exposition durch Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R67:Dämpfe können Schläfrigkeit und Benommenheit verursachen.
R65:Gesundheitsschädlich: kann beim Verschlucken Lungenschäden verursachen.
R38:Reizt die Haut.
R11:Leichtentzündlich.

S-Sätze Betriebsanweisung:

S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S62:Bei Verschlucken kein Erbrechen herbeiführen. Sofort ärztlichen Rat einholen und Verpackung oder dieses Etikett vorzeigen.

Chemische Eigenschaften

Pure parathion is a pale yellow liquid with a faint odor of garlic, while technical parathion is a deep brown to yellow liquid. It is sparingly soluble in water, but soluble in alcohols, aromatic hydrocarbons, esters, ethers, n-hexane, dichloromethane, 2-propanol, toluene,and ketones. Parathion is one of the most acutely toxic pesticides and the US EPA has classifi ed parathion as an RUP, meaning it should only be handled by qualifi ed, trained, and certifi ed workers. In January 1992, the US EPA announced the cancellation of parathion for all uses on fruit, nut, and vegetable crops. Parathion was used for the control of pests of fruits, nuts, and vegetable crops. The only uses retained are those on alfalfa, barley, corn, cotton, sorghum, soybeans, sunfl owers, and wheat. Further, to reduce exposure of agricultural workers, parathion may only be applied to these crops by commercially certifi ed aerial applicators and treated crops may not be harvested by hand. Parathion is a broad spectrum, organophosphate pesticide used to control many insects and mites.

Chemische Eigenschaften

Parathion is a clear liquid when fresh; pale yellow to dark brown liquid with a garlic-like odor. Commercial formulations use carrier solvents that may change the physical properties shown.

Physikalische Eigenschaften

Pale yellow to dark brown liquid with a garlic-like odor. Robeck et al. (1965) reported odor threshold concentrations of 3 and 36 ppm for technical and pure grades, respectively.

Verwenden

Parathion is an organophosphate insecticide used on cotton, rice and fruit trees.

Verwenden

Insecticide; acaricide.

Allgemeine Beschreibung

Light-yellow liquid, Parathion turn solid at 6° C, a deadly poison by all routes. Organic phosphate insecticide, acts as an inhibitor of cholinesterase.

Allgemeine Beschreibung

Parathion, O,O-diethyl O-p-nitrophenylphosphorothioate (Thiophos), is a yellow liquid that is freelysoluble in aromatic hydrocarbons, ethers, ketones, esters,and alcohols but practically insoluble in water, petroleumether, kerosene, and the usual spray oils. It is decomposedat a pH above 7.5. Parathion is used as an agricultural insecticide.It is a relatively weak inhibitor of cholinesterase;however, enzymes present in liver microsomes and insecttissues convert parathion (pI50<4) to paraoxon, a more potentinhibitor of cholinesterase (pI50>8).64 Parathion is alsometabolized by liver microsomes to yield p-nitrophenol anddiethylphosphate; the latter is inactive as an irreversiblecholinesterase inhibitor.

Air & Water Reaktionen

Parathion is slightly soluble in water.

Reaktivität anzeigen

Pure parathion is a pale yellow liquid with a faint odour of garlic, while the technical parathion is a deep brown to yellow liquid. It is sparingly soluble in water but soluble in alcohols, aromatic hydrocarbons, esters, ethers, n-hexane, dichloromethane, 2-propanol, toluene, and ketones.
Violent reaction when PARATHION is used as solvent to dissolve endrin. When heated to decomposition Parathion emits very toxic fumes of oxides of sulfur, phosphorus and nitrogen [Lewis, 3rd ed., 1993, p. 984].

Health Hazard

Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Health Hazard

Extremely toxic; acetylcholinesterase inhibitor; toxic symptoms include nausea,vomiting, diarrhea, excessive salivation,lacrimation, constriction of the pupils, bronchoconstriction, convulsions, coma, and respiratory failure; metabolizes to paraoxon; oralLD50 value (rats): 2 mg/kg, LD50 value, skin(rats): 6.8 mg/kg RCRA Waste Number P089.

Health Hazard

Parathion is highly toxic by all routes of exposure. Parathion, like all organophosphate pesticides, inhibits acetylcholinesterase and alters cholinergic synaptic transmission at neuroeffector junctions (muscarinic effects), at skeletal myoneural junctions, in autonomic ganglia (nicotinic effects), and in the CNS. Exposures to parathion cause symptoms of poisoning that include, but are not limited to, abdominal cramps, vomiting, diarrhea, pinpoint pupils, blurred vision, excessive sweating, salivation and lacrimation, wheezing, excessive tracheobronchial secretions, agitation, seizures, bradycardia or tachycardia, muscle twitching and weakness, and urinary bladder and fecal incontinence. Seizures are much more common in children than in adults. Severe exposures cause loss of consciousness, coma, excessive bronchial secretions, respiratory depression, cardiac irregularity, eventually leading to death. Occupational workers and the general public with health disorders and abnormalities, such as cardiovascular, liver or kidney diseases, glaucoma, or CNS, are at an increased risk of parathion poisoning. Further, high environmental temperatures enhance the severity of parathion poisoning.

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.

Landwirtschaftliche Anwendung

Insecticide, Acaricide: The U.S. EPA announced in November, 2000, the cancellation of ethyl parathion immediately on seed corn and the eventual phase out for its use in other pesticide products by the end of 2000. By the end of October, 2003, the U.S. EPA phased out its use to control insects and mites on alfalfa, barley, corn, canola, sorghum, soybeans, sunflowers and wheat. Also used to control nuisance birds. Not listed for use in EU countries. Not registered for use in the U.S. There are 25 global suppliers.

Handelsname

(There are 921 active and canceled/transferred labels registered with the U.S. EPA) ACC 3422®; ALKRON®[C]; ALLERON®; AMERICAN CYANAMID 3422®; APHAMITE®; ARALO®; B 404®; BAY E-605®; BAYER E-605®; BLADAN®; BLADAN F®; COMPOUND 3422®; COROTHION®; CORTHION®; COR-THION®; DANTHION®; DREXEL PARATHION 8E®; E 605®; E 605 F®; ECATOX®; EKATIN WF & WF ULV®; EKATOX®; ETHLON®; ETILON®; FIGHTER®; FOLIDOL®; FOLIDOL E®; FOLIDOL E-605®; FOLIDOL E&E 605®; FOLIDOL OIL®; FOSFERMO®; FOSFERNO®; FOSFEX®; FOSFIVE®; FOSOVA®; FOSTERN®; FOSTOX®; GEARPHOS®; GENITHION®; IDA SEIS-TRES 6-3®; KALPHOS®; KOLODUST®[C]; KYPTHION®; LETHALAIRE G-54®; LIROTHION®; MURFOS®; MURPHOS®; NIRAN®[C]; NIUIF 100®; NITROSTIGMINE®; NOURITHION®; NOVAFOS-M®; OLEOFOS 20®; OLEOPARATHENE®; OLEOPARATHION®; ORTHOPHOS®; PAC®; PACOL®; PARA-KILL®[C]; PARAMAR®; PARA-TOX®[C]; PANTHION®; PARADUST®; PARAPHOS®; PARAWET®; PENNCAP E®; PESTOX PLUS®; PETHION®; PHOSKIL®; PLEOPARAPHENE®; RHODIASOL®; RHODIATOX®; RHODIATROX®; SEIS-TRES 6-3®; SELEPHOS®; SOPRATHION®; STATHION®; SULPHOS®; SUPER RODIATOX®; T-47®; THIOMEX®; THIOPHOS®; THIOPHOS® 3422; TIOFOS®; TOX 47®; TOXOL®; VAPOPHOS®; VITREX®; WOPROPHOS®

Kontakt-Allergie

One case was reported of a bullous contact dermatitis due to ethylparathion.

Sicherheitsprofil

A deadly poison by all routes. Human systemic effects by ingestion: general anesthetic; pulmonary effects; and hdney, ureter, bladder effects, true cholinesterase changes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Human mutation data reported. A cholinesterase inhibitor. Parathon, like the other organic phosphorus poisons, acts as an irreversible inhibitor of the enzyme cholinesterase and thus allows the accumulation of large amounts of acetylcholine. When a critical level of cholinesterase depletion is reached, grave symptoms appear. Whether death is actually caused entirely by cholinesterase depletion or by the disturbance of a number of enzymes is not yet known. Recovery is apparently complete if a poisoned animal or human has time to re-form a critical amount of cholinesterase. The organism exposed remains susceptible to relatively low dosages of parathion untd the chohnesterase has regenerated. Small doses at frequent intervals are, therefore, more or less additive. There is no indication that, when recovery from a given exposure is entirely complete, the exposed organism is prejudiced in any way. Combustible when exposed to heat or flame. Violent reaction with endrin. Highly dangerous; shock can shatter the container, releasing the contents A broad spectrum insecticide in agricultural applications. When heated to decomposition it emits highly toxic fumes of NOx, POx, and SOx.

mögliche Exposition

A severely hazardous pesticide formulation. Those exposed include those engaged in manufacture,formulation and application of this broad spectrum insecticide. This material has also been used as a chemical warfare agent.

Enzyminhibitor

This insecticide (FW = 291.26 g/mol; CAS 56-38-2), also known as E605, phosphostigmine, and phosphorothioic acid O,O-diethyl O-(4-nitrophenyl) ester, is a cholinesterase inhibitor. Primary Mode of Action: Like other phosphorothioate organo-phosphorus pesticides, parathion is metabolized by cytochrome P450s, either through a dearylation reaction to form an inactive metabolite, or through a desulfuration to form the active oxon metabolite, paraoxon-ethyl (e.g., (CH3CH2–O–)2P(=O)–O–C6H4–NO2). The latter is a highly effective mechanism-based acetylcholinesterase inhibitor. The primary enzymes involved in parathion bioactivation are CYP2B6, CYP2C19, and CYP1A2. CAUTION: Parathion is highly toxic by all routes of exposure. Its use and that of related organophosphorus compounds annually accounts for 200,000 deaths worldwide, mainly farmworkers. The lowest dosage with detectible toxic effects in humans is 240 μg/kg (< 0.1 ounce). The most common cause of death is failure to maintain adequate oxygenation. Clinical signs of organophosphate poisoning include excess salivation, lacrimation, abdominal pain, vomiting, intestinal hypermotility, and diarrhea. The consensus treatment is early resuscitation with atropine and use of a mechanical respirator, supplemented with oxygen, to provide adequate oxygenation of vital tissues. Target(s): acetylcholinesterase (1- 5); (Ca2+/Mg2+)-ATPase; carboxylesterase; cholinesterase, or butyrylcholinesterase; CYP1A1; CYP3A2; CYP3A4; CYP3A27; CYP2B1; CYP2C6; CYP2C11; cytochrome P450; nicotinic acetylcholine receptor; and photosynthetic system

Environmental Fate

Biological. Initial hydrolysis products include diethyl-O-thiophosphoric acid, p-nitrophenol (Sethunathan, 1973, 1973a; Munnecke and Hsieh, 1976; Sethunathan et al., 1977; Verschueren, 1983) and the biodegradation products p-aminoparathion and p-aminophenol (Sethunathan, 1973; Laplanche et al., 1981; Nelson, 1982). Mixed bacterial cultures were capable of growing on technical parathion as the sole carbon and energy source (Munnecke and Hsieh, 1976). Three oxidative pathways were reported. The primary degradative pathway is initial hydrolysis to yield p-nitrophenol and diethylthiophosphoric acid. The secondary pathway involves the formation of paraoxon (diethyl p-nitrophenyl phosphate)
which subsequently undergoes hydrolysis to yield p-nitrophenol and diethylphosphoric acid. The third degradative pathway involved reduction of parathion under low oxygen conditions to yield p-amino-parathion followed by hydrolysis to p-aminophenol and die
A Flavobacterium sp. (ATCC 27551), isolated from rice paddy water, degraded parathion to p-nitrophenol. The microbial hydrolysis half-life of this reaction was <1 hour (Sethunathan and Yoshida, 1973; Forrest, 1981). Sharmila et al. (1989) isolated a Baci
In both soils and water, chemical- and biological-mediated reactions transform parathion to paraoxon (Alexander, 1981). Parathion was reported to biologically hydrolyze to p-nitrophenol in different soils under flooded conditions (Sudhakar-Barik and Sethunathan, 1978; Ferris and Lichtenstein, 1980)
p-Nitrophenol, paraoxon and three unidentified metabolites were identified in a model ecosystem containing algae, Daphnia magna, fish, mosquito and snails (Yu and Sanborn, 1975)

Versand/Shipping

UN3278 Organophosphorus compound, liquid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required, Potential Inhalation Hazard (Special Provision 5).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 materials.

Inkompatibilitäten

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the presence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials. Attacks some plastics, rubbers, and coatings. Rapidly hydrolyzed by alkalis.

Waste disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. 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. One manufacturer recommends the use of a detergent in a 5% trisodium phosphate solution for parathion disposal and cleanup problems. For parathion disposal in general, however, the recommended method is incineration (816°C, 0.5 second minimum for primary combustion; 1204°C, 1.0 second for secondary combustion) with adequate scrubbing and ash disposal facilities.

Parathion (ISO) Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Parathion (ISO) Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 0)Lieferanten
Firmenname Telefon Fax E-Mail Land Produktkatalog Edge Rate

56-38-2(Parathion (ISO))Verwandte Suche:


  • phosphorothioicacid,o,o-diethylo-(p-nitrophenyl)ester
  • PhosphorothionicacidO,O-diethyl-O-(4-nitro-phenyl)ester
  • Phosphostigmine
  • Rcra waste number P089
  • rcrawastenumberp089
  • Rhodiasol
  • Rhodiatox
  • Rhodiatrox
  • selephos
  • soprathion
  • soprothion
  • Stabilized ethyl parathion
  • THIOPHOS(R)
  • SNP(R)
  • O,O-DIETHYL-O-P-NITROPHENYL PHOSPHOROTHIOATE
  • O,O-Diethyl-O-(p-nitrophenyl)thionophosphate
  • O,O-DIETHYL O-(4-NITROPHENYL) PHOSPHOROTHIOATE
  • ORTHOPHOS(R)
  • PARAPHOS(R)
  • PARATHION
  • stabilizedethylparathion
  • Stathion
  • deoxynucleoside triphosphate, 10MM Mix
  • deoxynucleoside triphosphate, 2.5MM Mix
  • Parathion standard in chloroforM
  • Parathion Solution, 100ppm
  • CleanAmp? dNTP
  • Parathion Solution, 1000ppm
  • PARATHION-ETHYL
  • PARATHION (TM)
  • NIRAN(R)
  • ETILON(R)
  • FOLIDOL(R)
  • Folidol
  • FOSFERNO(R)
  • E-605(R)
  • ETHYL PARATHION
  • ETHYLPARATHIONE
  • ETHYL PARATHION(R)
  • diethyl 4-nitrophenyl phosphorothionate
  • DNTP MIXTURE
  • DNTP(R)
  • BLADAN(R)
  • APHAMITE(R)
  • ACC 3422(R)
  • ALKRON(R)
  • 1605
  • AAT
  • AATP
  • AC 3422
  • ac3422
  • ACC 3422
  • acc3422
  • Alkron
  • Alleron
  • American Cyanamid 3422
  • americancyanamid3422
  • Aphamite
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