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Dimethyl itaconate

Cat. No. M9765
Dimethyl itaconate Structure
Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
25g USD 40  USD40 In stock
50g USD 60  USD60 In stock
100g USD 90  USD90 In stock
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Quality Control & Documentation
Biological Activity

Dimethyl itaconate may be used in functionalization of isotactic poly(propylene). Dimethyl itaconate undergoes enantioselective Rh(I)-catalyzed hydrogenation which can be enhanced by appropriate choice of substituents on aromatic ring of (1,2-diarylphosphinoxy)cyclohexane. It was used in crosslinking of polyesters: poly(isosorbide itaconate)and poly(isosorbide itaconate-co-succinate).

Product Citations
Chemical Information
Molecular Weight 158.15
Formula C7H10O4
CAS Number 617-52-7
Solubility (25°C) Slightly soluble in water
Storage 2-8°C, dry, protect from light, 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] Qian Wang, et al. J Mol Med (Berl). The anti-inflammatory dvrg dimethyl itaconate protects against colitis-associated colorectal cancer

[2] M Sendra, et al. Fish Shellfish Immunol. Immune-responsive gene 1 (IRG1) and dimethyl itaconate are involved in the mussel immune response

[3] Ping-Chang Kuo, et al. J Neuroinflammation. Dimethyl itaconate, an itaconate derivative, exhibits immunomodulatory effects on neuroinflammation in experimental autoimmune encephalomyelitis

[4] Yepin Zhao, et al. Adv Mater. A Polymerization-Assisted Grain Growth Strategy for Efficient and Stable Perovskite Solar Cells

[5] Caijun Zhao, et al. Microb Pathog. Dimethyl itaconate protects against lippolysacchride-induced mastitis in mice by activating MAPKs and Nrf2 and inhibiting NF-κB signaling pathways

[6] T. V. RajanBabu, et al. J Org Chem. Electronic Effects in Asymmetric Catalysis: Structural Studies of Precatalysts and Intermediates in Rh-Catalyzed Hydrogenation of Dimethyl Itaconate and Acetamidocinnamic Acid Derivatives Using C(2)-Symmetric Diarylphosphinite Ligands

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