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45681

Supelco

Tetramethrin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C19H25NO4
CAS Number:
7696-12-0
Molecular Weight:
331.41
Beilstein/REAXYS Number:
8807938
EC Number:
231-711-6
MDL number:
MFCD00084635
UNSPSC Code:
41116107
PubChem Substance ID:
329756895
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

C\C(C)=C\C1C(C(=O)OCN2C(=O)C3=C(CCCC3)C2=O)C1(C)C

InChI

1S/C19H25NO4/c1-11(2)9-14-15(19(14,3)4)18(23)24-10-20-16(21)12-7-5-6-8-13(12)17(20)22/h9,14-15H,5-8,10H2,1-4H3

InChI key

CXBMCYHAMVGWJQ-UHFFFAOYSA-N

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Application

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

Legal Information

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

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Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - STOT SE 2 Inhalation

target_organs

Nervous system

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

ppe

Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG9070
BCCB4529
BCBX5211
BCBX0898
SZBD123XV

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J H Song et al.
Brain research, 712(2), 258-264 (1996-03-18)
The differential effects of the pyrethroid tetramethrin on tetrodotoxin-sensitive (TTX-S) and tetrodotoxin-resistant (TTX-R) single sodium channel currents in rat dorsal root ganglion (DRG) neurons were investigated using the outside-out configuration of patch-clamp technique. Channel conductances were 10.7 and 6.3 pS
Ali Niazi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 69(4), 1165-1169 (2007-07-27)
The simultaneous determination of cypermethrin and tetramethrin mixtures by using spectrophotometric method is a difficult problem in analytical chemistry, due to spectral interferences. By multivariate calibration methods, such as partial least squares (PLS) regression, it is possible to obtain a
J H Song et al.
Brain research, 708(1-2), 29-37 (1996-02-05)
Type I and type II pyrethroids and dichlorodiphenyltrichloroethane (DDT) are known to modulate the sodium channel to cause the hyperexcitatory symptoms of poisoning in animals. However, since the degrees to which neuronal sodium channel parameters are altered differ, a question
Xu Zhe et al.
Journal of chromatographic science, 46(9), 783-786 (2008-11-15)
A high-performance liquid chromatography method is presented for the enantioseparation and quantitation of tetramethrin. The separation is achieved on amylose 3,5-dimethylphenyl-carbamate CSP (Chiralpak AD-H column) using a mobile phase consisting of a mixture of n-hexane-ethanol-2-propanol (99:0.9:0.1, v/v/v). Baseline chiral separation
I V Tabarean et al.
The Journal of pharmacology and experimental therapeutics, 299(3), 988-997 (2001-11-21)
Pyrethroid insecticides may be classified into two groups: type I pyrethroids lack a cyano group in the alpha-position, whereas type II pyrethroids have a cyano group. Both types prolong the sodium channel current thereby causing hyperexcitability, yet details of modulation
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