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Merck

91588

Supelco

N-(n-Butyl)thiophosphoric triamide

analytical standard

Sinónimos:

N-Butylphosphorothioic triamide, N-Butylthiophosphoric triamide

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About This Item

Fórmula empírica (notación de Hill):
C4H14N3PS
Número de CAS:
Peso molecular:
167.21
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

impurities

≤1.0% water (calculated from elemental analysis)

mp

56-58 °C (lit.)

format

neat

storage temp.

2-8°C

SMILES string

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)

InChI key

HEPPIYNOUFWEPP-UHFFFAOYSA-N

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General description

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.

Application

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.

Recommended products

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.

pictograms

Health hazardCorrosion

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Repr. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

204.8 °F - closed cup

flash_point_c

96 °C - closed cup


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Visite la Librería de documentos

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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