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45324

Supelco

Amitrol

PESTANAL®, analytical standard

Synonym(s):

3-Amino-1,2,4-triazole, 1,2,4-Triazol-3-amine, 3-AT, Amitrol

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About This Item

Empirical Formula (Hill Notation):
C2H4N4
CAS Number:
61-82-5
Molecular Weight:
84.08
Beilstein/REAXYS Number:
107687
EC Number:
200-521-5
MDL number:
MFCD00005230
UNSPSC Code:
41116107
PubChem Substance ID:
329756647
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

150-153 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Nc1nc[nH]n1

InChI

1S/C2H4N4/c3-2-4-1-5-6-2/h1H,(H3,3,4,5,6)

InChI key

KLSJWNVTNUYHDU-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

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Repr. 2 - STOT RE 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK3505
BCCG7166
BCBV2744
SZBC202XV
SZBB329XV

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S Gayatridevi et al.
Plant physiology and biochemistry : PPB, 52, 154-161 (2012-01-17)
The relationship between salicylic acid level catalases isoforms chickpea cv. ICCV-10 infected with Fusarium oxysporum f. sp. ciceri was investigated. Pathogen-treated chickpea plants showed high levels of SA compared with the control. Two isoforms of catalases in shoot extract (CAT-IS
Hope A Cole et al.
Nucleic acids research, 39(22), 9521-9535 (2011-09-02)
We have used paired-end sequencing of yeast nucleosomal DNA to obtain accurate genomic maps of nucleosome positions and occupancies in control cells and cells treated with 3-aminotriazole (3AT), an inducer of the transcriptional activator Gcn4. In control cells, 3AT-inducible genes
Xinyu Deng et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50(9), 3073-3078 (2012-06-13)
Carbon tetrachloride (CCl(4)) has been used extensively to study xenobiotic-induced oxidative liver injury. Catalase (CAT) is a major antioxidant enzyme while aminotriazole (ATZ) is commonly used as a CAT inhibitor. In the present study, the effects of ATZ on CCl(4)-induced
G Ermondi et al.
Journal of chromatography. A, 1252, 84-89 (2012-07-17)
Molecular Interaction Fields (MIFs) based descriptors can be conveniently used to characterize and compare chromatographic scales. In this study, Quantitative Structure-Retention Relationships (QSRR) for eight different chromatographic systems were obtained with VolSurf+ descriptors and Partial Least Squares (PLS). A new
Kathryn M Gauthier et al.
American journal of physiology. Renal physiology, 301(4), F765-F772 (2011-07-15)
Cytochrome P-450 metabolites of arachidonic acid, the epoxyeicosatrienoic acids (EETs) and hydrogen peroxide (H(2)O(2)), are important signaling molecules in the kidney. In renal arteries, EETs cause vasodilation whereas H(2)O(2) causes vasoconstriction. To determine the physiological contribution of H(2)O(2), catalase is
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