22421-85-8 Usage
Description
Phosphoric triamide, hexabutylis a chemical compound formed from the reaction of phosphorus pentoxide with butylamine. It is characterized by its six butyl groups attached to the phosphorus atom, making it a highly nonpolar and hydrophobic molecule. This unique structure allows it to be used as a reagent in organic synthesis, particularly in the production of phthalimides and other nitrogen-containing compounds. However, due to its potential as an irritant to the skin, eyes, and respiratory system, proper handling and safety precautions should be taken when working with this compound.
Uses
Used in Organic Synthesis:
Phosphoric triamide, hexabutylis used as a reagent in organic synthesis for the production of phthalimides and other nitrogen-containing compounds. Its unique structure allows it to facilitate various chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Solvent Applications:
Due to its nonpolar and hydrophobic nature, phosphoric triamide, hexabutylis used as a solvent in reactions that require such properties. Its ability to dissolve a wide range of compounds makes it a versatile and useful solvent in various chemical processes.
Used in Catalyst Applications:
Phosphoric triamide, hexabutylis also used as a catalyst in certain chemical reactions. Its unique structure allows it to lower the activation energy of reactions, thereby increasing the reaction rate and improving the overall efficiency of the process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, phosphoric triamide, hexabutylis used as a reagent in the synthesis of various pharmaceutical compounds. Its ability to facilitate the production of nitrogen-containing compounds makes it a valuable tool in the development of new drugs and medications.
Used in Chemical Research:
Phosphoric triamide, hexabutylis also used in chemical research for the study of various chemical reactions and processes. Its unique properties make it an interesting subject for research, and it can provide valuable insights into the behavior of nonpolar and hydrophobic molecules in different chemical environments.
Check Digit Verification of cas no
The CAS Registry Mumber 22421-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22421-85:
(7*2)+(6*2)+(5*4)+(4*2)+(3*1)+(2*8)+(1*5)=78
78 % 10 = 8
So 22421-85-8 is a valid CAS Registry Number.
22421-85-8Relevant articles and documents
Metal catalysis in oxidation by peroxides. 24. Extraction of aqueous peroxomolybdenum species into organic media and their reactivity
Bortolini, Olga,Bragante, Letanzio,Di Furia, Fulvio,Modena, Giorgio
, p. 1189 - 1195 (1986)
The effect of the lipophilicity and coordinating ability of neutral ligands, belonging to the classes of phosphoric amides and pyridine oxides, on the extraction of neutral oxidants molybdenum(VI)-peroxo complexes from an aqueous acidic phase to an organic one, has been studied.The nature of the Mo(VI)-peroxo species present both in aqueous and organic phase has also been investigated.Sizable amounts of mineral acid, added to adjust pH, may be extracted into the organic phase.The various factors affecting this process such as the nature of the acid added, the organic solvent and the neutral ligand, as well as the effect of this feature on the partition of the oxidant between the two phases are briefly discussed.
Rapid Analysis of Tetrakis(dialkylamino)phosphonium Stability in Alkaline Media
Womble, C. Tyler,Kang, Jamie,Hugar, Kristina M.,Coates, Geoffrey W.,Bernhard, Stefan,Noonan, Kevin J. T.
, p. 4038 - 4046 (2017/10/30)
Hydroxide-stable organic cations are crucial components for ion-transport processes in electrochemical energy systems, and the tetrakis(dialkylamino)phosphonium cation is a promising candidate for this application. These phosphoniums are known to be highly resistant to alkaline media; however, very few investigations have systematically evaluated how these cations decompose in the presence of hydroxide or alkoxide anions. The excellent stability of several tetraaminophosphoniums in 2 M KOH/CH3OH at 80 °C led us to design experiments for the rapid assessment of phosphonium degradation in homogeneous solution and under phase-transfer conditions. The analysis illustrated how substituents around the cation core affect both degradation pathways and rates. β-H elimination and direct attack at the phosphorus atom are the most common degradation pathways observed in an alcoholic solvent, while α-H abstraction and direct attack are observed under phase-transfer conditions (PhCl and 50 wt % NaOH/H2O). The collected data provided a relative stability comparison for this family of cations to enable future design improvements and illustrated the utility of using multiple tests for degradation studies.
