C4255
Creatinine
anhydrous, ≥98%
Synonym(s):
2-Amino-1-methyl-2-imidazolin-4-one, 2-Imino-1-methylimidazolidin-4-one, 2-Imino-N-methylhydantoin
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About This Item
Empirical Formula (Hill Notation):
C4H7N3O
CAS Number:
Molecular Weight:
113.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-466-7
Beilstein/REAXYS Number:
112061
MDL number:
Product Name
Creatinine, anhydrous, ≥98%
InChI
1S/C4H7N3O/c1-7-2-3(8)6-4(7)5/h2H2,1H3,(H2,5,6,8)
InChI key
DDRJAANPRJIHGJ-UHFFFAOYSA-N
SMILES string
CN1CC(=O)N=C1N
grade
anhydrous
assay
≥98%
form
powder
mp
295 °C (dec.) (lit.)
Quality Level
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Application
Creatinine can be used as:
- A nitrogen donor building block to prepare nitrogen-containing heterocyclic derivatives.
- A reactant to synthesize donor-acceptor type carbon nitride copolymer, which is used as a photocatalyst in hydrogen production.
- A starting material to prepare creatol(2-amino-1,5-dihydro-5-hydroxy methylimidazol-4-one) via creatinine chloramine.
- A reactant to synthesize 3-substituted-3-hydroxyisatins by gold-catalyzed aldolization with various isatins.
General description
Creatinine is a breakdown product formed by the degradation of creatine phosphate from muscles. The kidneys extract creatinine from the body by filtering almost all of it from the blood and excreting it in the urine. Serum creatinine is the most commonly used indicator for renal functioning. In chemical synthesis, creatinine is used as a heterocyclic nitrogenous compound that produces electron-rich and highly basic creatinine derivatives.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
554.0 °F - closed cup
flash_point_c
290 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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A Simple Conversion of Creatinine to Creatol via Creatinine Chloroamine
Ienaga K, et al.
Australian Journal of Chemistry, 68(2), 248-253 (2015)
Constructing creatinine-derived moiety as donor block for carbon nitride photocatalyst with extended absorption and spatial charge separation
Zong X, et al.
Applied Catalysis. B, Environmental, 291 (2021)
Study of Creatinine and its 5-Alkoxy Analogs: Structure and Conformational Studies in the Solid and Solution States by X-Ray Crystallography, NMR, UV and Mass Spectrometry
Arakali AV, et al.
Nucleosides, nucleotides & nucleic acids, 16(12), 2193-2218 (1997)
A review on creatinine measurement techniques
Mohabbati-Kalejahi E, et al.
Talanta, 97, 1-8 (2012)
Gold-catalyzed addition reaction between creatinine and isatin: A sustainable and green chemistry approach for the diastereoselective synthesis of 3-substituted-3-hydroxyisatins
Parthasarathy K, et al.
Chinese Journal of Catalysis, 38(5), 775-783 (2017)
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