94295
3-Ureidopropionic acid
≥98.0% (T)
Synonym(s):
N-Carbamoyl-β-alanine
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About This Item
Linear Formula:
NH2CONHCH2CH2COOH
CAS Number:
Molecular Weight:
132.12
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1705263
InChI
1S/C4H8N2O3/c5-4(9)6-2-1-3(7)8/h1-2H2,(H,7,8)(H3,5,6,9)
SMILES string
NC(=O)NCCC(O)=O
InChI key
JSJWCHRYRHKBBW-UHFFFAOYSA-N
assay
≥98.0% (T)
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
170-175 °C (dec.)
application(s)
peptide synthesis
Quality Level
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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B Zarabian et al.
Analytical biochemistry, 166(1), 113-119 (1987-10-01)
Two modified procedures for the colorimetric quantitation of citrulline aimed primarily at the assay of ornithine transcarbamylase were developed. Both methods give highly reproducible results in a short period of time since color is developed in 25 min at 100
J Yaplito-Lee et al.
Molecular genetics and metabolism, 93(2), 190-194 (2007-10-30)
Beta-ureidopropionase deficiency (McKusick 606673) is an autosomal recessive condition caused by mutations in the UPB1 gene. To date, five patients have been reported, including one putative case detected through newborn screening. Clinical presentation includes neurological and developmental problems. Here, we
S H Moolenaar et al.
Magnetic resonance in medicine, 46(5), 1014-1017 (2001-10-25)
In this work, NMR investigations that led to the discovery of a new inborn error of metabolism, beta-ureidopropionase (UP) deficiency, are reported. 1D (1)H-NMR experiments were performed using a patient's urine. 3-Ureidopropionic acid was observed in elevated concentrations in the
Y Inoue et al.
Biological mass spectrometry, 20(10), 593-601 (1991-10-01)
Using fast atom bombardment (FAB) and tandem mass spectrometry (MS/MS), we examined 12 synthetic N-carbamoylamino acids (CAA) as tert-butyldimethylsilyl (TBDMS) derivatives. In FAB mass spectrometry and FAB MS/MS, spectra of protonated molecules for CAA provide specific cleavages involving the TBDMS
G Waldmann et al.
Analytical biochemistry, 188(1), 233-236 (1990-07-01)
A sensitive assay for beta-ureidopropionase based on derivatization of the reaction product beta-alanine with phenylisothiocyanate has been developed. Purification of the resulting phenylthiocarbamoyl-beta-alanine is achieved on a LiChrospher 100 C18 reversed-phase high-performance liquid chromatography column using an isocratic elution system.
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