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Fórmula empírica (notación de Hill):
C4H7N3O
Número CAS:
Peso molecular:
113.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-466-7
Beilstein/REAXYS Number:
112061
MDL number:
Assay:
≥98%
Form:
powder
Servicio técnico
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Permítanos ayudarlegrade
anhydrous
Quality Level
assay
≥98%
form
powder
mp
295 °C (dec.) (lit.)
SMILES string
CN1CC(=O)N=C1N
InChI
1S/C4H7N3O/c1-7-2-3(8)6-4(7)5/h2H2,1H3,(H2,5,6,8)
InChI key
DDRJAANPRJIHGJ-UHFFFAOYSA-N
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.
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.
Clase de almacenamiento
11 - 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)
A review on creatinine measurement techniques
Mohabbati-Kalejahi E, et al.
Talanta, 97, 1-8 (2012)