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15270

Sigma-Aldrich

Biuret

98% (Contains ≤10%(w/w) Triuret)

Synonym(s):

Allophanic acid amide, Carbamoylurea

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About This Item

Linear Formula:
NH2CONHCONH2
CAS Number:
108-19-0
Molecular Weight:
103.08
Beilstein:
1703510
EC Number:
203-559-0
MDL number:
MFCD00007946
UNSPSC Code:
12352100
PubChem Substance ID:
57647348
NACRES:
NA.22

Assay

98% (Contains ≤10%(w/w) Triuret)

form

powder or crystals

impurities

≤1% water

mp

185-190 °C (dec.) (lit.)

SMILES string

NC(=O)NC(N)=O

InChI

1S/C2H5N3O2/c3-1(6)5-2(4)7/h(H5,3,4,5,6,7)

InChI key

OHJMTUPIZMNBFR-UHFFFAOYSA-N

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Application

Biuret (Carbamoylurea) was used as a source of dietary nitrogen in purified diets for steers.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Urea

Evaluation of urea, biuret, urea phosphate and uric acid as NPN sources for cattle.
R R Oltjen et al.
The Journal of nutrition, 94(2), 193-202 (1968-02-01)
Shuping Jin et al.
Journal of agricultural and food chemistry, 59(1), 322-327 (2010-12-16)
In this investigation, a novel water-insoluble slow-release fertilizer, biuret polyphosphoramide (BPAM), was formulated and synthesized from urea, phosphoric acid (H(3)PO(4)), and ferric oxide (Fe(2)O(3)). The structure of BPAM was characterized by Fourier transform infrared (FTIR) spectroscopy. Subsequently, a coated slow-release
S J Woltman et al.
Journal of pharmaceutical and biomedical analysis, 14(1-2), 155-164 (1995-12-01)
An electrochemical detection method was applied to the determination of the synthetic peptide TP9201 (Telios Pharmaceuticals). The method utilizes reversed-phase HPLC, followed by post-column formation of Cu(II)-peptide complexes to render peptides electrochemically active via the Cu(III/II) couple. TP9201 is cyclic
C L Kuckel et al.
Biochimica et biophysica acta, 1162(1-2), 143-148 (1993-03-05)
Uremia has been implicated in cataractogenesis due to protein carbamylation by cyanate derived from urea. The present study was designed to directly identify the effects of carbamylation on actin polymerization and the possible contribution to cataract formation. The susceptibility of
S M Rutherfurd et al.
Amino acids, 32(2), 235-242 (2006-07-27)
The stability of felinine, an amino acid present in feline urine, was investigated. Synthetic felinine was unstable in the urine of a selection of mammals. Felinine was found to stable in feline urine in which urea had been degraded. Synthetic
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