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Key Documents

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:
Molecular Weight:
103.08
Beilstein/REAXYS Number:
1703510
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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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Evaluation of urea, biuret, urea phosphate and uric acid as NPN sources for cattle.
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The use of electrophoresis to monitor monoclonal immunoglobulins migrating in the β fraction may be difficult because of their comigration with transferrin and complement proteins. Immunoassays specific for IgGκ, IgGλ, IgAκ, IgAλ, IgMκ, and IgMλ heavy/light chain (HLC) were validated
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
Nóra Felföldi et al.
Carbohydrate research, 345(2), 208-213 (2009-12-17)
O-peracetylated 1-(beta-D-glucopyranosyl)-5-phenylbiuret was prepared in the reaction of O-peracetylated beta-D-glucopyranosylisocyanate and phenylurea. The reaction of O-peracetylated N-beta-D-glucopyranosylurea with phenylisocyanate furnished the corresponding 1-(beta-D-glucopyranosyl)-3,5-diphenyl- as well as 3-(beta-D-glucopyranosyl)-1,5-diphenyl biurets besides 1-(beta-D-glucopyranosyl)-3-phenylurea. O-Peracetylated 1-(beta-D-glucopyranosyl)-5-(beta-D-glycopyranosyl)biurets were obtained in one-pot reactions of O-peracetylated beta-D-glucopyranosylamine
Christian Johannessen et al.
Dalton transactions (Cambridge, England : 2003), (10)(10), 1028-1033 (2007-02-28)
Vibrational absorption (VA) and vibrational circular dichroism (VCD) spectroscopy was applied in the analysis of vibrational and low lying electronic transitions of a triplet ground state cobalt(III) coordination compound. The spectroscopic measurements were performed on the tetrabutylammonium salt of (6S,7S)-1,3,5,8,10,12-hexaaza-2,4,9,11-tetraoxo-6,7-diphenyl-dodecanato(4-)cobaltate(III)

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