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Merck

45305

Supelco

Dicrotophos

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C8H16NO5P
Número de CAS:
Peso molecular:
237.19
Beilstein:
1880084
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

Línea del producto

PESTANAL®

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

agriculture
environmental

Formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

COP(=O)(OC)O\C(C)=C\C(=O)N(C)C

InChI

1S/C8H16NO5P/c1-7(6-8(10)9(2)3)14-15(11,12-4)13-5/h6H,1-5H3/b7-6+

Clave InChI

VEENJGZXVHKXNB-VOTSOKGWSA-N

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Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Productos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Información legal

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogramas

Skull and crossbonesEnvironment

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Código de clase de almacenamiento

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificados de análisis (COA)

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Visite la Librería de documentos

Dietrich E Lorke et al.
Current pharmaceutical design, 23(23), 3432-3439 (2016-11-02)
Reversible cholinesterase inhibitors, when given prophylactically before exposure to organophosphates, are able to decrease organophosphate-induced mortality. However, the efficacy of pyridostigmine, the only pre-treatment substance approved by the US Federal Drug Administration, is unsatisfactory. In search of a better prophylactic
Moneen M Jones et al.
Journal of economic entomology, 111(2), 829-835 (2018-01-24)
To assess the toxicity of bifenthrin and four mixtures of insecticides to tarnished plant bug, we used an insecticide dip method of green bean to treat adults of a laboratory colony; mortality was assessed after 48 h. LC50s for imidacloprid
E F Hill
Journal of wildlife diseases, 25(4), 580-585 (1989-10-01)
Blood plasma cholinesterase (ChE) activity is a sensitive indicator of exposure to organophosphorus and carbamate insecticides. Effects of sex and storage of samples were studied as sources of variability by treating breeding Japanese quail (Coturnix japonica) with 3 mg of
A L Kilpatrick et al.
Journal of economic entomology, 98(3), 814-820 (2005-07-19)
Certain neonicotinoids are used in cotton, Gossypium hirsutum (L.), to control various piercing-sucking pests. We conducted field studies using three neonicotinoids (acetamiprid, thiamethoxam, and imidacloprid) and an organophosphate (dicrotophos) to assess the activity of these insecticides against nontarget arthropods, particularly
E L Flickinger et al.
Journal - Association of Official Analytical Chemists, 67(4), 827-828 (1984-07-01)
About 1100 birds of 12 species died from organophosphate poisoning in Matagorda County on the Texas Gulf Coast in March and May 1982. Birds died from feeding on rice seed that was illegally treated with dicrotophos or monocrotophos and placed

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