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Key Documents

45324

Supelco

Amitrol

PESTANAL®, analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C2H4N4
Numero CAS:
Peso molecolare:
84.08
Beilstein:
107687
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

150-153 °C (lit.)

applicazioni

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

Nc1nc[nH]n1

InChI

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

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Applicazioni

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

Note legali

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

Pittogrammi

Health hazardEnvironment

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Aquatic Chronic 2 - Repr. 2 - STOT RE 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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


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Certificati d'analisi (COA)

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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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