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Sodium diethyldithiocarbamate trihydrate

Cat. No. M7752
Sodium diethyldithiocarbamate trihydrate Structure
Synonym:

DIECA

Size Price Availability Quantity
5g USD 20  USD20 In stock
10g USD 30  USD30 In stock
25g USD 45  USD45 In stock
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Quality Control & Documentation
Biological Activity

Sodium diethyldithiocarbamate trihydrate is a chelating agent, generally used in mobilizing toxic metals from the human tissues and experimental animals. Sodium diethyldithiocarbamate trihydrate inhibits induction of macrophage nitric oxide synthase.

Sodium diethyldithiocarbamate (DIECA) has been used as a JA biosynthesis inhibitor in plants and likely inhibits the JA pathway by shunting 13(S)-hydroperoxylinolenic acid to 13-hydroxylinolenic, thereby sharply reducing the precursor pool leading to cyclization and eventual synthesis of JA.

Sodium diethyldithiocarbamate trihydrate was used during the synthesis of N-allylpeptides.

Application: Spin trap used in conjunction with Fe2+ to detect NO in brain, kidney, liver, and other tissues. Simultaneous direct measurement of NO* and pO2 has been reported. A copper chelator, it has been used to quantitate copper in biological materials by ESR and is an inhibitor of superoxide dismutase, ascorbate oxidase, and other enzymes.

Chemical Information
Molecular Weight 225.31
Formula (C2H5)2NCSSNa · 3H2O
CAS Number 20624-25-3
Solubility (25°C) Water 100 mg/mL
Storage RT, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Xiantao Niu, et al. Controllable Synthesis of Defect-Rich CoMoS Catalysts with Different Morphologies for the Ultradeep Hydrodesulfurization of 4,6-Dimethydibenzothiophene

[2] Jin Zhang, et al. The Jasmonic Acid Pathway Positively Regulates the Polyphenol Oxidase-Based Defense against Tea Geometrid Caterpillars in the Tea Plant (Camellia sinensis)

[3] Ahmed B M Ibrahim, et al. Synthesis, structural and antimicrobial studies of binary and ternary complexes of a new tridentate thiosemicarbazone

[4] Yan Wang, et al. Transcriptome Sequencing Reveals Candidate NF-κB Target Genes Involved in Repeated Cocaine Administration

[5] Bhupesh Sharma, et al. Defensive effect of natrium diethyldithiocarbamate trihydrate (NDDCT) and lisinopril in DOCA-salt hypertension-induced vascular dementia in rats

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