Bis(tributylammonium) pyrophosphate
TRIBUTYLAMMONIUM PYROPHOSPHATE
CAS: 5975-18-8
Molecular Formula: C24H58N2O7P2
Bis(tributylammonium) pyrophosphate - Names and Identifiers
| Name | TRIBUTYLAMMONIUM PYROPHOSPHATE |
| Synonyms | TRIBUTYLAMMONIUM PYROPHOSPHATE PYROPHOSPHATE, TRIBUTYLAMMONIUM Tri-n-butylammonium pyrophosphate, Bis(tributylaMMoniuM) Pyrophosphate |
| CAS | 5975-18-8 |
Bis(tributylammonium) pyrophosphate - Physico-chemical Properties
| Molecular Formula | C24H58N2O7P2 |
| Molar Mass | 548.674 |
| Storage Condition | -20℃ |
| Use | Uses tributylammonium pyrophosphate is an organic intermediate, which has been reported to be useful in the preparation of a base-modified nucleotide. Tributylammonium pyrophosphate is a phosphorylating reagent used in the synthesis of phosphorylated deoxynucleosides. Used as reactants in the following reactions: enzymatic synthesis of 3 '-deoxy-apio-nucleic acid duplex synthesis of deoxynucleoside S-methylphosphonic acid preparation of a fluorescent non-nucleotide ATP analog N-methyl anthranilamide ethyl triphosphate due to its low water content and high solubility in organic solvents, it is therefore useful for the synthesis of triphosphates. |
Bis(tributylammonium) pyrophosphate - Nature
| storage conditions | -20°C |
Last Update：2024-04-10 22:29:15
Bis(tributylammonium) pyrophosphate - Preparation
tetrasodium pyrophosphate salt (26.6g,0.1mol) is dissolved in deionized water (500mL). the aqueous solution passes through a strong ion exchange column (pk216 proton type), combines the stream containing pyrophosphoric acid, forms salt with n-tributylamine (37.1g,0.2mol), and concentrates the eluent into oil by a rotary evaporator. The oil substance is carried with water by 1, 4-dioxane (100mL) and repeated with water for 3 times to obtain the oil substance tributylammonium pyrophosphate (quantitative).
Last Update：2024-04-10 22:29:15
Bis(tributylammonium) pyrophosphate - Security information
| WGK Germany | 3 |
Last Update：2024-04-10 22:29:15
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View History
Bis(tributylammonium) pyrophosphate
2-甲基恶唑-5-羧酸
邻氨基对硝基苯甲酸
3-FORMYL-2-METHOXYPHENYLBORONIC ACID
ammoniumferrocyanide[(nh4)4(fe(cn)6)]
Chromate(2-), [3-[(5-chloro-2-hydroxyphenyl) azo]-4-hydroxy-6-[(1-oxo-2-propenyl)amino]-2 -naphthalenesulfonato(3-)][1-[(2-hydroxy-4-nitropheny l)azo]-2-naphthalenolato(2-)]-, dihydrogen
2-甲基恶唑-5-羧酸
邻氨基对硝基苯甲酸
3-FORMYL-2-METHOXYPHENYLBORONIC ACID
ammoniumferrocyanide[(nh4)4(fe(cn)6)]
Chromate(2-), [3-[(5-chloro-2-hydroxyphenyl) azo]-4-hydroxy-6-[(1-oxo-2-propenyl)amino]-2 -naphthalenesulfonato(3-)][1-[(2-hydroxy-4-nitropheny l)azo]-2-naphthalenolato(2-)]-, dihydrogen