94317-64-3,MFCD00269941
Catalog No.:AA0036MP

94317-64-3 | N-(n-Butyl)thiophosphoric triamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
95%
in stock  
$10.00   $7.00
- +
10g
95%
in stock  
$12.00   $8.00
- +
25g
95%
in stock  
$25.00   $17.00
- +
100g
97%
in stock  
$48.00   $34.00
- +
500g
97%
in stock  
$175.00   $123.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0036MP
Chemical Name:
N-(n-Butyl)thiophosphoric triamide
CAS Number:
94317-64-3
Molecular Formula:
C4H14N3PS
Molecular Weight:
167.2128
MDL Number:
MFCD00269941
SMILES:
CCCCNP(=S)(N)N
Properties
Properties
 
BP:
277.4°C at 760 mmHg  
Form:
Solid  
MP:
58-60°C  
Stability:
Stench  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
110  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.6  

Upstream Synthesis Route

[1]Patent:CN105399767,2016,A,.Locationinpatent:Paragraph0045;0047

[2]Patent:US2011/196172,2011,A1,.Locationinpatent:Page/Pagecolumn4

[3]ChemischeBerichte,1956,vol.89,p.1768,1770

[4]Patent:US2011/28761,2011,A1,.Locationinpatent:Page/Pagecolumn4

[5]Patent:CN105440073,2016,A,.Locationinpatent:Paragraph0038;0041

[1]Patent:CN105254664,2016,A,.Locationinpatent:Paragraph0062;0063

[2]Patent:US2011/196172,2011,A1,.Locationinpatent:Page/Pagecolumn3

[1]Patent:WO2010/45895,2010,A2,.Locationinpatent:Page/Pagecolumn11

[1]Patent:CN105131031,2017,B,.Locationinpatent:Paragraph0033;0035;0036;0037;0045;0048;0050

[1]Patent:US2008/287709,2008,A1,.Locationinpatent:Page/Pagecolumn7

[2]Patent:US2008/287709,2008,A1,.Locationinpatent:Page/Pagecolumn7

Downstream Synthesis Route

[1]Patent:CN105399767,2016,A.Locationinpatent:Paragraph0045;0047

[2]Patent:US2011/196172,2011,A1.Locationinpatent:Page/Pagecolumn4

[3]ChemischeBerichte,1956,vol.89,p.1768,1770

[4]Patent:US2011/28761,2011,A1.Locationinpatent:Page/Pagecolumn4

[5]Patent:CN105440073,2016,A.Locationinpatent:Paragraph0038;0041

[1]Patent:US2008/287709,2008,A1.Locationinpatent:Page/Pagecolumn7

[2]Patent:US2008/287709,2008,A1.Locationinpatent:Page/Pagecolumn7

[1]Patent:WO2010/45895,2010,A2.Locationinpatent:Page/Pagecolumn8

[1]Patent:WO2010/45895,2010,A2.Locationinpatent:Page/Pagecolumn11

Literature

Title: Effectiveness of urease inhibition on the abatement of ammonia, nitrous oxide and nitric oxide emissions in a non-irrigated Mediterranean barley field.

Journal: Chemosphere 20120901

Title: The physiological implications of urease inhibitors on N metabolism during germination of Pisum sativum and Spinacea oleracea seeds.

Journal: Journal of plant physiology 20120501

Title: Ammonia volatilization from urea-application influenced germination and early seedling growth of dry direct-seeded rice.

Journal: TheScientificWorldJournal 20120101

Title: Efficiency of urease and nitrification inhibitors in reducing ammonia volatilization from diverse nitrogen fertilizers applied to different soil types and wheat straw mulching.

Journal: Journal of the science of food and agriculture 20110701

Title: Short term physiological implications of NBPT application on the N metabolism of Pisum sativum and Spinacea oleracea.

Journal: Journal of plant physiology 20110301

Title: Ureic nitrogen transformation in multi-layer soil columns treated with urease and nitrification inhibitors.

Journal: Journal of agricultural and food chemistry 20090610

Title: Effect of N-(n-butyl) thiophosphoric triamide and 3,4 dimethylpyrazole phosphate on gaseous emissions from grasslands under different soil water contents.

Journal: Journal of environmental quality 20090101

Title: Structural characteristics of phosphoramide derivatives as urease inhibitors. Requirements for activity.

Journal: Journal of agricultural and food chemistry 20080924

Title: Viability of zoonotic pathogens Escherichia coli and Salmonella in swine manure slurries with and without a urease inhibitor and thymol.

Journal: Letters in applied microbiology 20080401

Title: Fabrication of molecular nanotemplates in self-assembled monolayers by extreme-ultraviolet-induced chemical lithography.

Journal: Small (Weinheim an der Bergstrasse, Germany) 20071201

Title: Combination of a urease inhibitor and a plant essential oil to control coliform bacteria, odour production and ammonia loss from cattle waste.

Journal: Journal of applied microbiology 20070201

Title: Determination of urease activity in soils by carbon dioxide release for ecotoxicological evaluation of contaminated soils.

Journal: Ecotoxicology (London, England) 20021001

Title: Inhibition of jack bean urease by N-(n-butyl) thiophosphorictriamide and N-(n-butyl) phosphorictriamide: determination of the inhibition mechanism.

Journal: Journal of enzyme inhibition 20011201

Quotation Request
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SDS
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Tags:94317-64-3 Molecular Formula|94317-64-3 MDL|94317-64-3 SMILES|94317-64-3 N-(n-Butyl)thiophosphoric triamide
Catalog No.: AA0036MP
94317-64-3,MFCD00269941
94317-64-3 | N-(n-Butyl)thiophosphoric triamide
Pack Size: 5g
Purity: 95%
in stock
$10.00 $7.00
Pack Size: 10g
Purity: 95%
in stock
$12.00 $8.00
Pack Size: 25g
Purity: 95%
in stock
$25.00 $17.00
Pack Size: 100g
Purity: 97%
in stock
$48.00 $34.00
Pack Size: 500g
Purity: 97%
in stock
$175.00 $123.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0036MP
Chemical Name: N-(n-Butyl)thiophosphoric triamide
CAS Number: 94317-64-3
Molecular Formula: C4H14N3PS
Molecular Weight: 167.2128
MDL Number: MFCD00269941
SMILES: CCCCNP(=S)(N)N
Properties
BP: 277.4°C at 760 mmHg  
Form: Solid  
MP: 58-60°C  
Stability: Stench  
Storage: Inert atmosphere;2-8℃;  
Complexity: 110  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.6  
Upstream Synthesis Route
6141-81-7    94317-64-3 

[1]Patent:CN105399767,2016,A,.Locationinpatent:Paragraph0045;0047

[2]Patent:US2011/196172,2011,A1,.Locationinpatent:Page/Pagecolumn4

[3]ChemischeBerichte,1956,vol.89,p.1768,1770

[4]Patent:US2011/28761,2011,A1,.Locationinpatent:Page/Pagecolumn4

[5]Patent:CN105440073,2016,A,.Locationinpatent:Paragraph0038;0041

109-73-9    94317-64-3 

[1]Patent:CN105254664,2016,A,.Locationinpatent:Paragraph0062;0063

[2]Patent:US2011/196172,2011,A1,.Locationinpatent:Page/Pagecolumn3

6141-81-7    94317-64-3    12125-02-9 

[1]Patent:WO2010/45895,2010,A2,.Locationinpatent:Page/Pagecolumn11

71363-38-7    94317-64-3 

[1]Patent:CN105131031,2017,B,.Locationinpatent:Paragraph0033;0035;0036;0037;0045;0048;0050

102-82-9    109-73-9    94317-64-3 

[1]Patent:US2008/287709,2008,A1,.Locationinpatent:Page/Pagecolumn7

[2]Patent:US2008/287709,2008,A1,.Locationinpatent:Page/Pagecolumn7

Downstream Synthesis Route
6141-81-7    94317-64-3 

[1]Patent:CN105399767,2016,A.Locationinpatent:Paragraph0045;0047

[2]Patent:US2011/196172,2011,A1.Locationinpatent:Page/Pagecolumn4

[3]ChemischeBerichte,1956,vol.89,p.1768,1770

[4]Patent:US2011/28761,2011,A1.Locationinpatent:Page/Pagecolumn4

[5]Patent:CN105440073,2016,A.Locationinpatent:Paragraph0038;0041

102-82-9    109-73-9    94317-64-3 

[1]Patent:US2008/287709,2008,A1.Locationinpatent:Page/Pagecolumn7

[2]Patent:US2008/287709,2008,A1.Locationinpatent:Page/Pagecolumn7

109-73-9    94317-64-3    3858-78-4 

[1]Patent:WO2010/45895,2010,A2.Locationinpatent:Page/Pagecolumn8

6141-81-7    94317-64-3    12125-02-9 

[1]Patent:WO2010/45895,2010,A2.Locationinpatent:Page/Pagecolumn11

Literature fold

Title: Effectiveness of urease inhibition on the abatement of ammonia, nitrous oxide and nitric oxide emissions in a non-irrigated Mediterranean barley field.

Journal: Chemosphere20120901

Title: The physiological implications of urease inhibitors on N metabolism during germination of Pisum sativum and Spinacea oleracea seeds.

Journal: Journal of plant physiology20120501

Title: Ammonia volatilization from urea-application influenced germination and early seedling growth of dry direct-seeded rice.

Journal: TheScientificWorldJournal20120101

Title: Efficiency of urease and nitrification inhibitors in reducing ammonia volatilization from diverse nitrogen fertilizers applied to different soil types and wheat straw mulching.

Journal: Journal of the science of food and agriculture20110701

Title: Short term physiological implications of NBPT application on the N metabolism of Pisum sativum and Spinacea oleracea.

Journal: Journal of plant physiology20110301

Title: Ureic nitrogen transformation in multi-layer soil columns treated with urease and nitrification inhibitors.

Journal: Journal of agricultural and food chemistry20090610

Title: Effect of N-(n-butyl) thiophosphoric triamide and 3,4 dimethylpyrazole phosphate on gaseous emissions from grasslands under different soil water contents.

Journal: Journal of environmental quality20090101

Title: Structural characteristics of phosphoramide derivatives as urease inhibitors. Requirements for activity.

Journal: Journal of agricultural and food chemistry20080924

Title: Viability of zoonotic pathogens Escherichia coli and Salmonella in swine manure slurries with and without a urease inhibitor and thymol.

Journal: Letters in applied microbiology20080401

Title: Fabrication of molecular nanotemplates in self-assembled monolayers by extreme-ultraviolet-induced chemical lithography.

Journal: Small (Weinheim an der Bergstrasse, Germany)20071201

Title: Combination of a urease inhibitor and a plant essential oil to control coliform bacteria, odour production and ammonia loss from cattle waste.

Journal: Journal of applied microbiology20070201

Title: Determination of urease activity in soils by carbon dioxide release for ecotoxicological evaluation of contaminated soils.

Journal: Ecotoxicology (London, England)20021001

Title: Inhibition of jack bean urease by N-(n-butyl) thiophosphorictriamide and N-(n-butyl) phosphorictriamide: determination of the inhibition mechanism.

Journal: Journal of enzyme inhibition20011201

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