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Imidacloprid-urea - 98%, high purity , CAS No.120868-66-8

  • ≥98%
Item Number
I413104
Grouped product items
SKUSizeAvailabilityPrice Qty
I413104-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$35.90
I413104-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$79.90
I413104-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$114.90
I413104-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$159.90
View related series
Drug Metabolite

Basic Description

Synonymsimidacloprid-urea|120868-66-8|1-[(6-CHLOROPYRIDIN-3-YL)METHYL]IMIDAZOLIDIN-2-ONE|Imidacloprid urea|1-((6-chloropyridin-3-yl)methyl)imidazolidin-2-one|CHEBI:83544|CHEMBL71188|575W874H6J|2-Imidazolidinone, 1-[(6-chloro-3-pyridinyl)methyl]-|1-((6-Chloro-3-py
Specifications & Purity≥98%
Biochemical and Physiological MechanismsImidacloprid-urea with a role as a marine xenobiotic metabolite, is the primary imidacloprid soil metabolite, whereas imidacloprid-olefin is the main plant-relevant metabolite and is more toxic to insects than imidacloprid.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Imidacloprid-urea with a role as a marine xenobiotic metabolite, is the primary imidacloprid soil metabolite, whereas imidacloprid-olefin is the main plant-relevant metabolite and is more toxic to insects than imidacloprid.

Associated Targets

NR3C1 Tclin Glucocorticoid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

VDR Tclin Vitamin D3 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR1H4 Tclin Bile acid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRNB2 Tclin Neuronal acetylcholine receptor subunit beta-2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 1-[(6-chloropyridin-3-yl)methyl]imidazolidin-2-one
INCHI InChI=1S/C9H10ClN3O/c10-8-2-1-7(5-12-8)6-13-4-3-11-9(13)14/h1-2,5H,3-4,6H2,(H,11,14)
InChi Key ADWTYURAFSWNSU-UHFFFAOYSA-N
Canonical SMILES C1CN(C(=O)N1)CC2=CN=C(C=C2)Cl
Isomeric SMILES C1CN(C(=O)N1)CC2=CN=C(C=C2)Cl
PubChem CID 15390532
Molecular Weight 211.65

Certificates

Certificate of Analysis(COA)

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8 results found

Lot NumberCertificate TypeDateItem
B2428397Certificate of AnalysisJan 22, 2024 I413104
B2428428Certificate of AnalysisJan 22, 2024 I413104
B2428433Certificate of AnalysisJan 22, 2024 I413104
B2428434Certificate of AnalysisJan 22, 2024 I413104
B2428437Certificate of AnalysisJan 22, 2024 I413104
B2428443Certificate of AnalysisJan 22, 2024 I413104
B2428446Certificate of AnalysisJan 22, 2024 I413104
B2428448Certificate of AnalysisJan 22, 2024 I413104

Safety and Hazards(GHS)

Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H302:Harmful if swallowed

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P301+P312:IF SWALLOWED: call a POISON CENTER/doctor/... IF you feel unwell.

Related Documents

Solution Calculators