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N-(n-Butyl)thiophosphoric triamide

analytical standard

Synonyme(s) :

N-Butylphosphorothioic triamide, N-Butylthiophosphoric triamide

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About This Item

Formule empirique (notation de Hill):
C4H14N3PS
Numéro CAS:
94317-64-3
Poids moléculaire :
167.21
Numéro MDL:
MFCD00269941
Code UNSPSC :
12352103
ID de substance PubChem :
329770057
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥98.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Impuretés

≤1.0% water (calculated from elemental analysis)

Pf

56-58 °C (lit.)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

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)

Clé InChI

HEPPIYNOUFWEPP-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Produits recommandés

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.

Pictogrammes

Health hazardCorrosion
GHS08,GHS05

Mention d'avertissement

Danger

Mentions de danger

H318,H361f

Classification des risques

Eye Dam. 1 - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

204.8 °F - closed cup

Point d'éclair (°C)

96 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
BCCL1512
BCCK4187
BCCF7516
BCCD6251
BCBZ9478

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Consulter la Bibliothèque de documents

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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