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MilliporeSigma

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:
462-88-4
Molecular Weight:
132.12
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
57653594
MDL number:
MFCD00043023
Beilstein/REAXYS Number:
1705263

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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

100

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Show Differences

1 of 4

This Item
2177946903715382
3-Ureidopropionic acid ≥98.0% (T)

Sigma-Aldrich

94295

3-Ureidopropionic acid

DL-3-Aminoisobutyric acid 98%

Sigma-Aldrich

217794

DL-3-Aminoisobutyric acid

Ureidosuccinic acid 98.0-102.0% (T)

Sigma-Aldrich

69037

Ureidosuccinic acid

Boc-β-Ala-OH ≥99.0% (TLC)

Sigma-Aldrich

15382

Boc-β-Ala-OH

form

powder

form

powder

form

-

form

solid

assay

≥98.0% (T)

assay

98%

assay

98.0-102.0% (T)

assay

≥99.0% (TLC)

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

200

mp

170-175 °C (dec.)

mp

179-182 °C (lit.)

mp

~175 °C (dec.)

mp

76-79 °C

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

-

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

-

application(s)

peptide synthesis

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM5160
BCCK0285
BCCH4115
BCCD6549
BCCB0601

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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.
C Schmidt et al.
Journal of inherited metabolic disease, 28(6), 1109-1122 (2006-01-26)
To evaluate the significance of inborn metabolic disorders of the pyrimidine degradation pathway, 450 children with unspecific neurological symptoms were comprehensively studied; 200 healthy children were recruited as controls. Uracil and thymine as well as their degradation products in urine
Improved colorimetric procedure for quantitating N-carbamoyl-beta-alanine with minimum dihydrouracil interference.
T P West et al.
Analytical biochemistry, 122(2), 345-347 (1982-05-15)
Simple method for the quantitative analysis of dihydropyrimidines and N-carbamyl-beta-amino acids in urine.
A H van Gennip et al.
Advances in experimental medicine and biology, 309B, 15-19 (1991-01-01)
M M Matthews et al.
The Journal of biological chemistry, 262(15), 7232-7237 (1987-05-25)
N-Carbamoyl-beta-alanine (NC beta A) amidohydrolase (EC 3.5.1.6) is regulated in opposing fashion by the substrate, NC beta A and the product, beta-alanine. The native enzyme from rat liver has a molecular weight of 235,000 in the absence of ligands. NC
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