n,n,n-tributyl-1-butanaminiumiodide
Tetrabutylammonium iodide
CAS: 311-28-4
Molecular Formula: C16H36IN
n,n,n-tributyl-1-butanaminiumiodide - Names and Identifiers
| Name | Tetrabutylammonium iodide |
| Synonyms | tbai Tetrabutylammonium i tetrabutyl-ammoniuiodide tetrabutylammonium iodid Tetrabutylazanium iodide Tetrabutylaminium·iodide tetranbutylammoniumiodide Tetrabutylammonium iodide tetra-n-butylammoniumjodid tetrabutyl ammonium iodide tetrabutylammoniumiodidegr tetra butyl ammonium iodide Tetra-n-butylammonium iodide tetran-butylammoniumiodidea.r. Tetra(but-1-yl)ammonium iodide n,n,n-tributyl-1-butanaminiuiodide n,n,n-tributyl-1-butanaminiumiodide Tetrabutylammonium iodide, HPLC grade 1-butanaminium,n,n,n-tributyl-,iodide Tetrabutylammonium iodide, extra pure TETRABUTYLAMMONIUM IODIDE extrapure AR |
| CAS | 311-28-4 |
| EINECS | 206-220-5 |
| InChI | InChI=1/C16H36N.HI/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1 |
| InChIKey | DPKBAXPHAYBPRL-UHFFFAOYSA-M |
n,n,n-tributyl-1-butanaminiumiodide - Physico-chemical Properties
| Molecular Formula | C16H36IN |
| Molar Mass | 369.37 |
| Density | 1.20 |
| Melting Point | 141-143°C(lit.) |
| Boling Point | 145.3℃[at 101 325 Pa] |
| Flash Point | 100℃ |
| Water Solubility | Soluble in water and methanol. Insoluble in benzene. |
| Solubility | Soluble in water and ethanol, slightly soluble in chloroform. |
| Vapor Presure | 0Pa at 25℃ |
| Appearance | White or brown powder |
| Color | White to cream |
| Odor | Amine like |
| Exposure Limit | ACGIH: TWA 0.01 ppm |
| Maximum wavelength(λmax) | ['λ: 290 nm Amax: 0.1', , 'λ: 300 nm Amax: 0.05', , 'λ: 320 nm Amax: 0.02', , 'λ: 500 |
| BRN | 3916152 |
| Storage Condition | Store below +30°C. |
| Stability | Stable. Incompatible with strong oxidizing agents. Light-sensitive. |
| Sensitive | Light Sensitive & Hygroscopic |
| MDL | MFCD00011636 |
| Physical and Chemical Properties | Density 1.20 melting point 141-150°C |
| Use | Used as a polarographic analysis reagent |
n,n,n-tributyl-1-butanaminiumiodide - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
| RTECS | BS5450000 |
| FLUKA BRAND F CODES | 8 |
| TSCA | Yes |
| HS Code | 29239000 |
| Toxicity | LD50 orally in Rabbit: 1990 mg/kg |
n,n,n-tributyl-1-butanaminiumiodide - Introduction
Easy to absorb moisture. It's irritating. Solubility in water <5%.
Last Update：2022-10-16 17:24:30
n,n,n-tributyl-1-butanaminiumiodide - Reference Information
| LogP | 0.869 at 25℃ |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| overview | tetrabutylammonium iodide (TBAI) is a commonly used phase transfer catalyst, which can increase the reaction rate or effectively promote a variety of chemical reactions. The reagent can be used as an iodine source to generate iodides needed for the reaction in situ, which can avoid the use of some unstable and expensive iodides. In addition, this reagent is also widely used in the dealkylation reaction of esters and ethers. |
| Properties | Tetrabutylammonium iodide is an organic ammonium compound, which is a white crystal or powder, stable at room temperature and pressure. Soluble in water. |
| application | tetrabutylammonium iodide is an organic ammonium compound, which can be used as a phase transfer catalyst and polarographic analysis reagent. TBAI as a phase transfer catalyst can effectively promote the alkylation of nucleophilic substrates such as alcohols, amines and phospholipids. In the two-phase reaction system, TBAI is more important as a phase transfer catalyst to promote the reaction. |
| Use | Used as polarographic analysis reagent Ion pair chromatography reagent, phase transfer catalyst, polarographic analysis reagent. Organic synthesis. |
| Production method | 1. In a round bottom flask with a reflux condenser, hold 200 ml of tri-n-butylamine and 100 ml of iodine n-butane. Heat on a steam bath for 65 hours, filter out the solids, wash with a small amount of ethyl acetate, and dissolve in the minimum amount of cold ethanol. The resulting solution was mixed with an equal volume of 10% potassium hydroxide ethanol solution and then poured into water. Part of the ethanol is evaporated under reduced pressure to obtain the iodide crystal. Recrystallized three times in anhydrous ethyl acetate to obtain 150 grams of product. |
Last Update：2024-04-10 22:29:15
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