Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

77951

Sigma-Aldrich

Imidazolepropionic acid

≥98.0% (GC)

Synonym(s):

1H-Imidazole-4-propanoic acid, 1H-Imidazole-5-propanoic acid, 3-(1H-Imidazol-4-yl)propionic acid, 3-(Imidazol-4(5)-yl)propionic acid, Deamino-histidine, Dihydrourocanic acid, NSC 66737

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C6H8N2O2
CAS Number:
1074-59-5
Molecular Weight:
140.14
EC Number:
214-045-0
MDL number:
MFCD18459271
UNSPSC Code:
12352106
PubChem Substance ID:
329768045
NACRES:
NA.25
Pricing and availability is not currently available.

Quality Level

100

Assay

≥98.0% (GC)

form

powder

storage temp.

2-8°C

SMILES string

OC(CCC1=CN=CN1)=O

InChI

1S/C6H8N2O2/c9-6(10)2-1-5-3-7-4-8-5/h3-4H,1-2H2,(H,7,8)(H,9,10)

InChI key

ZCKYOWGFRHAZIQ-UHFFFAOYSA-N

Biochem/physiol Actions

Imidazolepropionic acid is a product of histidine metabolism, which may involve oxidation or transamination

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCK7700
BCCH4693
BCCC9841
BCBS3337V
BCBQ8345V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

I Antener et al.
International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 53(2), 199-209 (1983-01-01)
The present study, as a part of a broader investigation on protein-energy-malnutrition (PEM) in rural Zaire, was undertaken in order to clarify varying aspects of histidine metabolism in patients suffering from protein-energy malnutrition (PEM). Measurement of histidine and its derivatives
A covalent nicotinamide adenine dinucleotide intermediate in the urocanase reaction.
L H Matherly et al.
Biochemistry, 21(11), 2789-2794 (1982-05-25)
A nitrogen-15 nuclear magnetic resonance study of the acid-base and tautomeric equilibriums of 4-substituted imidazoles and its relevance to the catalytic mechanism of .alpha.-lytic protease.
Roberts, J. D. , et al.
Journal of the American Chemical Society, 104, 3945-3949 (1982)
Alexander V Bogachev et al.
Molecular microbiology, 86(6), 1452-1463 (2012-10-20)
Interpretation of the constantly expanding body of genomic information requires that the function of each gene be established. Here we report the genomic analysis and structural modelling of a previously uncharacterized redox-metabolism protein UrdA (SO_4620) of Shewanella oneidensis MR-1, which
Imidazolepropionic acid as a urinary metabolite of L-histidine.
N P SEN et al.
Biochemical and biophysical research communications, 9, 257-261 (1962-10-17)
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service