Creatine methyl ester

Creatine methyl ester
	source ↗
Names
	IUPAC name Methyl N-(aminoiminomethyl)-N-methylglycine
Identifiers
CAS Number	341553-87-5 Y; 132478-02-5 (HCl) N;
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	9861656 Y;
PubChem CID	11686929;
CompTox Dashboard (EPA)	DTXSID40470581 ;
	InChI InChI=1S/C5H11N3O2/c1-8(5(6)7)3-4(9)10-2/h3H2,1-2H3,(H3,6,7) Y Key: JQIVVNGNZVUVJC-UHFFFAOYSA-N Y; InChI=1/C5H11N3O2/c1-8(5(6)7)3-4(9)10-2/h3H2,1-2H3,(H3,6,7) Key: JQIVVNGNZVUVJC-UHFFFAOYAK;
	SMILES NC(N(C)CC(OC)=O)=N; O=C(OC)CN(C(=[N@H])N)C;
Properties
Chemical formula	C5H11N3O2
Molar mass	145.162 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Creatine methyl ester is the methyl ester derivative of the amino acid creatine. It can be prepared by the esterification of creatine with methanol. ¹

By undergoing an esterification process with methanol, this compound seeks to enhance creatine's absorption rate in the body. Creatine esters, like creatine methyl ester, have been studied for their potential to improve bioavailability when compared to standard creatine monohydrate.²

References

Feng, Liang; Hu, Jiwen; Liu, Zhilei; Zhao, Fabao; Liu, Guojun (June 2007). "Preparation and properties of optically active poly(N-methacryloyl l-leucine methyl ester)". Polymer. 48 (13): 3616–3623. doi:10.1016/j.polymer.2007.04.064. ISSN 0032-3861.
"Creatine Methyl Ester". combatcreatine.com. Retrieved 2024-11-10.

[1] Feng, Liang; Hu, Jiwen; Liu, Zhilei; Zhao, Fabao; Liu, Guojun (June 2007). "Preparation and properties of optically active poly(N-methacryloyl l-leucine methyl ester)". Polymer. 48 (13): 3616–3623. doi:10.1016/j.polymer.2007.04.064. ISSN 0032-3861.

[2] "Creatine Methyl Ester". combatcreatine.com. Retrieved 2024-11-10.

1

2

See also

References