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91481

Supelco

Malathion

certified reference material, TraceCERT®

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About This Item

Formule empirique (notation de Hill):
C10H19O6PS2
Numéro CAS:
121-75-5
Poids moléculaire :
330.36
Numéro Beilstein :
1804525
Numéro CE :
204-497-7
Numéro MDL:
MFCD00036233
Code UNSPSC :
41116107
ID de substance PubChem :
329770043
Nomenclature NACRES :
NA.24

Qualité

certified reference material
TraceCERT®

Niveau de qualité

300

Gamme de produits

TraceCERT®

Durée de conservation

limited shelf life, expiry date on the label

Conditions de stockage

(storage under argon)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Conditions d'expédition

dry ice

Température de stockage

-10 to -25°C

Chaîne SMILES 

CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC

InChI

1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3

Clé InChI

JXSJBGJIGXNWCI-UHFFFAOYSA-N

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Catégories apparentées

Description générale

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Application

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

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Informations légales

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

Pictogrammes

Exclamation markEnvironment
GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H302,H317,H410

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCF1728
BCBT9976
BCBL8366V
BCBG2078V
BCBG2078

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Guang-Mao Shen et al.
Pest management science, 68(12), 1553-1563 (2012-09-26)
The oriental fruit fly, Bactrocera dorsalis, is a major pest that infects fruits and agricultural products worldwide. The latest resistance monitoring of B. dorsalis from mainland China has identified high levels of resistance to insecticides. In this study, the biochemical
Maya L Groner et al.
Ecological applications : a publication of the Ecological Society of America, 23(6), 1443-1454 (2013-10-24)
For the past several decades, amphibian populations have been decreasing around the globe at an unprecedented rate. Batrachochytrium dendrobatidis (Bd), the fungal pathogen that causes chytridiomycosis in amphibians, is contributing to amphibian declines. Natural and anthropogenic environmental factors are hypothesized
Leslie C Alvarez et al.
Journal of medical entomology, 50(5), 1031-1039 (2013-11-05)
Resistance to the insecticides deltamethrin and malathion and the enzymes associated with metabolic resistance mechanisms were determined in four field populations of Aedes aegypti (L.) from western Venezuela during 2008 and 2010 using the bottle assay and the microplate biochemical
Mingjing Sun et al.
Journal of hazardous materials, 237-238, 140-146 (2012-09-12)
The dissipation behavior of the two enantiomers of malathion was elucidated in five plant species using enantioselective high performance liquid chromatography (HPLC), and the acute toxicity of the individual enantiomers toward earthworms and honeybees was studied. The calculated LC(50) values
Hu Zhang et al.
Journal of agricultural and food chemistry, 60(41), 10188-10195 (2012-09-27)
An enantioselective method is presented for the determination of isocarbophos in soil by liquid chromatography coupled with tandem mass spectrometry. The pesticide residues in soil samples were extracted with acetonitrile, and complete enantioseparation was obtained on an amylose tris(3,5-dimethylphenylcarbamate) chiral
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