N-Desmethylthiamethoxam

Chemodex
Product Code: CDX-C0134
Product Group: Other Biochemicals
Supplier: Chemodex
CodeSizePrice
CDX-C0134-M05050 mg£108.00
Quantity:
CDX-C0134-M250250 mg£401.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Alternate Names/Synonyms:
TMX-dm; CGA330050; 3-(2-Chloro-1,3-thiazol-5-ylmethyl)-1,3,5-oxadiazinan-4-ylidene(nitro)amine
Appearance:
Off-white powder.
CAS:
171103-04-1
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H302
InChi:
InChI=1S/C7H8ClN5O3S/c8-6-9-1-5(17-6)2-12-4-16-3-10-7(12)11-13(14)15/h1H,2-4H2,(H,10,11)
InChiKey:
LOXCNVOJGRNBFX-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 171103-04-1. Formula: C7H8ClN5O3S. MW: 277.69. Synthetic. Neonicotinoid insecticide. Interacts with insect nicotinic acetylcholine receptors (nAChRs), but is about 25 times less potent than thiamethoxam as an insecticide. Shown to be almost as active as the insecticide imidacloprid. Can be used as a reference compound.
MDL:
MFCD18384948
Molecular Formula:
C7H8ClN5O3S
Molecular Weight:
277.69
Package Type:
Vial
Precautions:
P264, P270, P301, P312, P330
Product Description:
Neonicotinoid insecticide. Interacts with insect nicotinic acetylcholine receptors (nAChRs), but is about 25 times less potent than thiamethoxam as an insecticide. Shown to be almost as active as the insecticide imidacloprid. Can be used as a reference compound.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
[O-][N+](=O)NC1=NCOCN1CC1=CN=C(Cl)S1
Solubility Chemicals:
Soluble in methanol.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) K.A. Ford & J.E. Casida; Chem. Res. Toxicol. 19, 1549 (2006) | (2) N. Simon-Delso, et al.; Environ. Sci. Pollut. Res. Int. 22, 5 (2015)

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