3-(3,4-Dichlorophenyl)-1-(methoxy-d3)-1-(methyl-d3)urea

≥98 atom % D

Reagent Code: #167244
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CAS Number 1219804-76-8

science Other reagents with same CAS 1219804-76-8

blur_circular Chemical Specifications

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Weight 255.13 g/mol
Formula C₉H₄D₆Cl₂N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a stable isotope-labeled internal standard in analytical chemistry, particularly in mass spectrometry-based assays. It aids in the accurate quantification of unlabeled analogs in environmental and biological samples by providing a reference with nearly identical chemical behavior but distinct mass detection. Commonly applied in pesticide metabolism studies and residue analysis due to its structural similarity to phenylurea herbicides. Its deuterated methyl and methoxy groups enhance detection sensitivity and reduce background interference.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿5,360.00
inventory 5mg
10-20 days ฿18,680.00

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3-(3,4-Dichlorophenyl)-1-(methoxy-d3)-1-(methyl-d3)urea
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Used as a stable isotope-labeled internal standard in analytical chemistry, particularly in mass spectrometry-based assays. It aids in the accurate quantification of unlabeled analogs in environmental and biological samples by providing a reference with nearly identical chemical behavior but distinct mass detection. Commonly applied in pesticide metabolism studies and residue analysis due to its structural similarity to phenylurea herbicides. Its deuterated methyl and methoxy groups enhance detection sen

Used as a stable isotope-labeled internal standard in analytical chemistry, particularly in mass spectrometry-based assays. It aids in the accurate quantification of unlabeled analogs in environmental and biological samples by providing a reference with nearly identical chemical behavior but distinct mass detection. Commonly applied in pesticide metabolism studies and residue analysis due to its structural similarity to phenylurea herbicides. Its deuterated methyl and methoxy groups enhance detection sensitivity and reduce background interference.

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