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DMTMM

CAT: 0804-HY-Y1168-01Size: 25 gDry Ice: NoHazardous: No
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CAT#:0804-HY-Y1168-01Size:25 g
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
DMTMM (4- (4,6-dimethoxy-1,3,5-triazine-2-yl) -4-methylmorpholinium chloride) is a coupling agent. DMTMM can activate carboxyl groups and promote the formation of amide bonds. DMTMM plays an important role in promoting the chemical modification of biomacromolecules such as polysaccharides and proteins. DMTMM can be used for research of tissue engineering, breast cancer, corneal regeneration, and biomaterials[1][2][3][4][5][6][7][8].
CAS Number
3945-69-5
Product Name Alternative
4- (4,6-Dimethoxy-1,3,5-triazin-2-yl) -4-methylmorpholinium chloride
UNSPSC
12352200
Hazard Statement
H302, H314
Target
Biochemical Assay Reagents
Type
Biochemical Assay Reagents
Related Pathways
Others
Field of Research
Cancer; Neurological Disease
Assay Protocol
https://www.medchemexpress.com/dmtmm.html
Purity
99.77
Solubility
DMSO : 50 mg/mL (ultrasonic; warming; heat to 60°C)
Smiles
C[N+]1(C2=NC(OC)=NC(OC)=N2)CCOCC1.[Cl-]
Molecular Formula
C10H17ClN4O3
Molecular Weight
276.72
Precautions
H302, H314
References & Citations
[1]Bergmeyer H U, et al. Biochemical reagents[M]//Methods of Enzymatic Analysis. Academic Press, 1965: 967-1037.|[2]Plaster E M, et al. DMTMM-mediated synthesis of norbornene-modified hyaluronic acid polymers to probe cell-hydrogel interactions. Carbohydrate Polymer Technologies and Applications, 2023, 6: 100360.|[3]Simpson FC, et al. Collagen analogs with phosphorylcholine are inflammation-suppressing scaffolds for corneal regeneration from alkali burns in mini-pigs. Commun Biol. 2021 May 21;4 (1) :608. |[4]Labre F, et al. DMTMM-mediated amidation of alginate oligosaccharides aimed at modulating their interaction with proteins. Carbohydr Polym. 2018 Mar 15;184:427-434. |[5]Magalhães MV, et al. In situ crosslinkable multi-functional and cell-responsive alginate 3D matrix via thiol-maleimide click chemistry. Carbohydr Polym. 2024 Aug 1;337:122144. |[6]Jo G, et al. Tumor Targeting with Methotrexate-Conjugated Zwitterionic Near-Infrared Fluorophore for Precise Photothermal Therapy. Int J Mol Sci. 2022 Nov 16;23 (22) :14127. |[7]Morieux P, et al. Synthesis and anticonvulsant activities of N-benzyl (2R) -2-acetamido-3-oxysubstituted propionamide derivatives. Bioorg Med Chem. 2008 Oct 1;16 (19) :8968-75.|[8]Hyun H, et al. Engineered beta-cyclodextrin-based carrier for targeted doxorubicin delivery in breast cancer therapy in vivo. Journal of Industrial and Engineering Chemistry, 2019, 70: 145-151.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Biochemical Assay Reagents
Clinical Information
No Development Reported