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Merck
CN

49866

Ammelide

analytical standard

Synonym(s):

2-Amino-1,3,5-triazine-4,6-dione

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About This Item

Empirical Formula (Hill Notation):
C3H4N4O2
CAS Number:
Molecular Weight:
128.09
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
85151701
EC Number:
211-456-7
MDL number:
Technical Service
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grade

analytical standard

Quality Level

assay

≥98.0% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

SMILES string

Nc1nc(O)nc(O)n1

InChI

1S/C3H4N4O2/c4-1-5-2(8)7-3(9)6-1/h(H4,4,5,6,7,8,9)

InChI key

YSKUZVBSHIWEFK-UHFFFAOYSA-N

General description

Ammelide can be synthesized via hydrolysis of 2-amino-4,6-dichloro-s-triazine in the presence of acid or base or by the reaction between urea and cyanogen iodide at 130-140 degrees.
Ammelide (AMD), a 1,3,5-triazine compound, is one of the hydrolysis by-products of melamine. It is most commonly found as an impurity in melamine and its structural analog, cyanuric acid feedstocks.

Application

Ammelide may be used as an analytical reference standard for the determination of the analyte in milk, milk products and infant formula using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Rapoport, L. and Smolin, ME
The Chemistry of Heterocyclic Compounds, 26 (2009)
Paul M Murphy et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(23), 9215-9220 (2009-05-28)
Altering the specificity of an enzyme requires precise positioning of side-chain functional groups that interact with the modified groups of the new substrate. This requires not only sequence changes that introduce the new functional groups but also sequence changes that
Mechanistic and spectral investigation on the deamination of ammeline and ammelide
Almatarneh HM, et al.
Computational & Theoretical Chemistry, 1117, 92-99 (2017)



Global Trade Item Number

SKUGTIN
49866-10MG04061832421841