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46114

Supelco

Transfluthrin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H12Cl2F4O2
CAS Number:
Molecular Weight:
371.15
EC Number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

FC1=C(F)C=C(F)C(F)=C1COC([C@H]2C(C)(C)[C@@H]2C=C(Cl)Cl)=O

InChI

1S/C15H12Cl2F4O2/c1-15(2)7(3-10(16)17)11(15)14(22)23-5-6-12(20)8(18)4-9(19)13(6)21/h3-4,7,11H,5H2,1-2H3/t7-,11+/m1/s1

InChI key

DDVNRFNDOPPVQJ-HQJQHLMTSA-N

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General description

Transfluthrin is a contact, pyrethroid ester insecticide, with repellent activity. Its mode of action involves a knock down effect in insect pests such as moths, cockroaches, flies, whitefly and mosquitoes.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Transfluthrin may be used as an analytical reference standard for the quantification of the analyte in biological and environmental samples using different chromatography techniques.

Recommended products

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.

Legal Information

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

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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John P Masalu et al.
Malaria journal, 19(1), 109-109 (2020-03-12)
Residents of malaria-endemic communities spend several hours outdoors performing different activities, e.g. cooking, story-telling or eating, thereby exposing themselves to potentially-infectious mosquitoes. This compromises effectiveness of indoor interventions, notably long-lasting insecticide-treated nets (LLINs) and indoor residual spraying (IRS). This study
Simultaneous determination of traces of pyrethroids, organochlorines and other main plant protection agents in agricultural soils by headspace solid-phase microextraction-gas chromatography
Fernandez-Alvarez M, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 1188(2), 154-163 (2008)
G Nentwig et al.
Journal of medical entomology, 54(1), 150-158 (2017-01-14)
One essential oil (clove oil), one skin repellent (icaridin), and one insecticide (transfluthrin) were tested for spatial repellent effects against non-blood-fed female Aedes aegypti (L.) mosquitoes. The compounds were tested in acetone dilution series using a Y-olfactometer, a double cage
Shirin Hooshfar et al.
Rapid communications in mass spectrometry : RCM, 31(19), 1573-1581 (2017-07-15)
Transfluthrin is a relatively non-toxic rapid-acting synthetic pyrethroid insecticide. It is widely used in household and hygiene products. A sensitive and accurate bioanalytical method is required for quantification of its concentration in plasma and its potential target organ, the brain
Wenwen Deng et al.
Food chemistry, 274, 891-899 (2018-10-31)
A series of new hydrophobic deep eutectic solvents (DESs), which are liquid at room temperature and have high density (>1.4 g mL-1), were synthesized using hexafluoroisopropanol (HFIP) as hydrogen-bond donor and l-carnitine/betaine as hydrogen-bond acceptor. Then these hydrophobic DESs were used as

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