ChemicalBook--->CAS DataBase List--->23505-41-1

23505-41-1

23505-41-1 Structure

23505-41-1 Structure
IdentificationMore
[Name]

Pirimiphos ethyl
[CAS]

23505-41-1
[Synonyms]

O-2-DIETHYLAMINO-6-METHYLPYRIMIDIN-4-YL O,O-DIETHYLPHOSPHOROTHIOATE
O,O-DIETHYL-O-[2-(DIETHYLAMINO)-6-METHYL-4-PYRIMIDINYL]-PHOSPHOROTHIOATE
PIRIMIPHOS-ETHYL
PP211
PRIMICID
PRIMICID(R)
Primote
2-diethylamino-6-methyl-4-pyrimidinyldiethylphosphorothioate
2-diethylamino-6-methylpyrimidin-4-yldiethylphosphorothionate
ai3-27698
caswellno334a
epapesticidechemicalcode108101
ethylpirimiphos
fernex
o-(2-(diethylamino)-6-methyl-4-pyrimidinyl)o,o-diethylphosphorothioate
o-(2-diethylamino)-6-methyl-4-pyrimidinyl)phosphorothioicacido,o-diethyleste
phosphorothioicacid,o-(2-(diethylamino)-6-methyl-4-pyrimidinyl)o,o-diethyle
phosphorothioicacid,o,o-diethylo-(2-(diethylamino)-6-methyl-4-pyrimidinyl)e
pirimifosethyl
pirimifos-ethyl
[EINECS(EC#)]

245-704-0
[Molecular Formula]

C13H24N3O3PS
[MDL Number]

MFCD00055295
[Molecular Weight]

333.39
[MOL File]

23505-41-1.mol
Chemical PropertiesBack Directory
[Appearance]

Pirimifos-ethyl is a straw-colored liquid
[Melting point ]

15-18 °C
[Boiling point ]

414.1±55.0 °C(Predicted)
[density ]

d20 1.14
[refractive index ]

nD25 1.520
[storage temp. ]

APPROX 4°C
[solubility ]

soluble in No Data available
[form ]

neat
[pka]

4.85±0.10(Predicted)
[Water Solubility ]

3.967mg/L(20 ºC)
[Merck ]

13,7580
[BRN ]

7141373
[Henry's Law Constant]

1.8×10-1 mol/(m3Pa) at 25℃, HSDB (2015)
[Major Application]

agriculture
environmental
[InChI]

1S/C13H24N3O3PS/c1-6-16(7-2)13-14-11(5)10-12(15-13)19-20(21,17-8-3)18-9-4/h10H,6-9H2,1-5H3
[InChIKey]

TZBPRYIIJAJUOY-UHFFFAOYSA-N
[SMILES]

CCOP(=S)(OCC)Oc1cc(C)nc(n1)N(CC)CC
[CAS DataBase Reference]

23505-41-1(CAS DataBase Reference)
[NIST Chemistry Reference]

Pirimiphos ethyl(23505-41-1)
[EPA Substance Registry System]

23505-41-1(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

T,N
[Risk Statements ]

R21:Harmful in contact with skin.
R25:Toxic if swallowed.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
[RIDADR ]

3018
[WGK Germany ]

3
[RTECS ]

TF1610000
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[Storage Class]

6.1C - Combustible, acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Dermal
Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1
[Hazardous Substances Data]

23505-41-1(Hazardous Substances Data)
[Toxicity]

LD50 in rats, mice, guinea pigs (mg/kg); 140-200, 105, 50-150 orally; dermally in rats: 1000-2000 mg/kg (Bullock)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Toluene-->Nitric acid-->Triethylamine-->Ethyl acetoacetate-->Xylene-->Diethylamine
Hazard InformationBack Directory
[General Description]

Straw colored liquid. Used as a pesticide.
[Reactivity Profile]

Organophosphates, such as PIRIMIFOS-ETHYL, 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]

Pirimifos-ethyl is an organophosphorus pesticide and is absorbed by the skin, as well as by the respiratory and gastrointestinal tracts. It is a cholinesterase inhibitor, acting on the nervous system.
[Potential Exposure]

A potential danger to those involved in the manufacture, formulation and application of this organophosphate soil insecticide.
[Fire Hazard]

As with other organophosphorus pesticides, container may explode in heat of fire. Heat may cause decomposition and evolution of highly toxic fumes of phosphorus oxides, nitrogen oxides and sulfur oxides. Decomposes above 266F.
[First aid]

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).
[Shipping]

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.
[Incompatibilities]

Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves. Medical observation is recommended for 2448 hours after breathing overexposure, as pulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consider administering a drug or other inhalation therapy.
[Chemical Properties]

Pirimifos-ethyl is a straw-colored liquid
[Uses]

Pirimiphos Ethyl is a pesticide used in the protection of crops. Insecticide.
[Definition]

ChEBI: Pirimiphos-ethyl is an organic thiophosphate.
[Production Methods]

The industrial synthesis of pirimiphos-ethyl begins with the preparation of the pyrimidine ring, typically formed via condensation of acetylacetone with guanidine or its derivatives to yield 2-diethylamino-6-methylpyrimidin-4-ol. This intermediate is then reacted with diethyl phosphorochloridothioate in the presence of a base such as triethylamine to form the phosphorothioate ester linkage. The reaction is carried out in organic solvents like toluene or acetonitrile under controlled temperature and pH conditions to ensure high yield and purity.
[Mechanism of action]

Broad-spectrum with contact and respiratory action. Acetylcholinesterase (AchE) inhibitor.
[Pesticide Type]

Insecticide; Acaricide
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

pirimiphos-ethyl(23505-41-1).msds
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

23505-41-1(sigmaaldrich)
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