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Supelco

Atrazine-desethyl-desisopropyl-2-hydroxy

PESTANAL®, analytical standard

Synonym(s):

4,6-Diamino-2-hydroxy-1,3,5-triazine, Ammeline

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About This Item

Empirical Formula (Hill Notation):
C3H5N5O
CAS Number:
Molecular Weight:
127.10
Beilstein:
607753
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Nc1nc(N)nc(O)n1

InChI

1S/C3H5N5O/c4-1-6-2(5)8-3(9)7-1/h(H5,4,5,6,7,8,9)

InChI key

MASBWURJQFFLOO-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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

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Hongkai Zhu et al.
Journal of hazardous materials, 373, 671-677 (2019-04-08)
Occurrence, spatial distribution, and temporal trends of melamine and its derivatives (ammeline, ammelide, and cyanuric acid) were investigated in surface sediment and two sediment cores collected from Lake Shihwa, South Korea. ∑Melamine (sum of melamine and its three derivatives) was
Hongkai Zhu et al.
Environment international, 123, 375-381 (2018-12-21)
Melamine is used extensively in household products, such as furniture, dinnerware, and food utensils. Several studies have shown that melamine adversely affects kidney function. Nevertheless, little is known about urinary melamine concentrations, and its temporal variability. In this study, 213
Jennifer L Seffernick et al.
Journal of bacteriology, 192(4), 1106-1112 (2009-12-22)
Melamine toxicity in mammals has been attributed to the blockage of kidney tubules by insoluble complexes of melamine with cyanuric acid or uric acid. Bacteria metabolize melamine via three consecutive deamination reactions to generate cyanuric acid. The second deamination reaction
Hongkai Zhu et al.
Environment international, 130, 104950-104950 (2019-06-30)
We determined the concentrations of melamine, ammeline, ammelide, and cyanuric acid in meat, fish and seafood, cereal products, beverages, cooking oil, and vegetables (n = 121) collected from Albany, New York, United States. In addition, food packaging (n = 24) and animal feed (n = 12)
Hongkai Zhu et al.
Environmental pollution (Barking, Essex : 1987), 245, 994-999 (2019-01-27)
Melamine-based resins are used extensively in laminates, plastics, coatings, glues, and dinnerware. Little is known, however, about the occurrence of melamine and its derivatives in the environment. In this study, a nationwide survey of melamine and its derivatives, namely ammeline

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