15270
Biuret
98% (Contains ≤10%(w/w) Triuret)
Synonym(e):
Alophansäureamid, Carbamoyl-harnstoff
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Alle Fotos(2)
About This Item
Lineare Formel:
NH2CONHCONH2
CAS-Nummer:
Molekulargewicht:
103.08
Beilstein:
1703510
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
Assay
98% (Contains ≤10%(w/w) Triuret)
Form
powder or crystals
Verunreinigungen
≤1% water
mp (Schmelzpunkt)
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)
InChIKey
OHJMTUPIZMNBFR-UHFFFAOYSA-N
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Verwandte Kategorien
Anwendung
Biuret (Carbamoylurea) was used as a source of dietary nitrogen in purified diets for steers.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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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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