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Supelco

N-(n-Butyl)thiophosphoric triamide

analytical standard

Sinonimo/i:

N-Butylphosphorothioic triamide, N-Butylthiophosphoric triamide

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About This Item

Formula empirica (notazione di Hill):
C4H14N3PS
Numero CAS:
Peso molecolare:
167.21
Numero MDL:
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥98.0% (HPLC)

Durata

limited shelf life, expiry date on the label

Impurezze

≤1.0% water (calculated from elemental analysis)

Punto di fusione

56-58 °C (lit.)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

S=P(NCCCC)(N)N

InChI

1S/C4H14N3PS/c1-2-3-4-7-8(5,6)9/h2-4H2,1H3,(H5,5,6,7,9)
HEPPIYNOUFWEPP-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

N-(n-Butyl)thiophosphoric triamide (nBPTT), an active ingredient in nitrogen stabilizers, is widely used as a urease inhibitor. Its mode of action involves the inhibition of urease enzyme thereby improving the efficiency of urea-containing fertilizers. nBPTT is also effective in increasing plant yields and reducing ammonia losses when employed with surface-applied urea and urea ammonium nitrate solutions.

Applicazioni

N-(n-Butyl)thiophosphoric triamide may be used as an analytical reference standard for the quantification of the analyte in soil samples, bovine milk and tissue extracts using chromatography techniques.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pittogrammi

Health hazardCorrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Eye Dam. 1 - Repr. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

204.8 °F - closed cup

Punto d’infiammabilità (°C)

96 °C - closed cup


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HPLC Method for the Analysis of the Urease Inhibitor N-(n-butyl) thiophosphoric Triamide and Its Metabolites
Douglass AE and Hendrickson LL
Journal of Agricultural and Food Chemistry, 39(12), 2318-2321 (1991)
Nondetectable or minimal detectable residue levels of N-(n-butyl) thiophosphoric triamide in bovine tissues and milk from a 28-d NBPT dosing study
Ligt dVJ, et al.
Translational behavioral medicine, 3(4), 1606-1616 (2019)
Simon Svane et al.
Scientific reports, 10(1), 8503-8503 (2020-05-24)
The nickel-dependent urease enzyme is responsible for the hydrolysis of urea to ammonia and carbon dioxide. A number of bacteria produce urease (ureolytic bacteria) and are associated with various infectious diseases and ammonia emissions from agriculture. We report the first
Lindsay M LaFave et al.
Cancer cell, 38(2), 212-228 (2020-07-25)
Regulatory networks that maintain functional, differentiated cell states are often dysregulated in tumor development. Here, we use single-cell epigenomics to profile chromatin state transitions in a mouse model of lung adenocarcinoma (LUAD). We identify an epigenomic continuum representing loss of

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