aluminium triethanolate (CAS 555-75-9) — formula C6H15AlO3, molecular weight 162.16; category inorganic chemicals.
| CAS Number | 555-75-9 |
|---|---|
| Molecular Formula | C6H15AlO3 |
| Molecular Weight | 162.16 |
| Boiling Point | 200 °C @ 6-8 mm Hg; 175-180 °C @ 3 mm Hg |
| Applications | Uses: Used in reduction of aldehydes and ketones and as a polymerization catalyst, [Merck Index], In reduction of aldehydes and ketones, as catalyst for polymerizations., Catalyst for preprn. of esters from aldehydes and alcoholysis of diketones., Catalyst, with compounds of early transition metals as Ziegler-Natta polymerization catalysts, intermediates in organic syntheses., Aluminum alkyls, Intermediates in organic phosphate insecticides, silicones, special saturated hydrocarbons, terpene alcohols, and organic acids., Aluminum alkyls are used for the preparation of Ziegler-Natta-type catalysts, in the polymerization of olefins, and in the alfen and alfol processes for the production of alpha-olefins and alcohols, respectively., Aluminum Alkyls, Methods of Manufacturing: ...By reacting aluminum powder with absolute ethanol in xylene using small amount of mercuric chloride and iodine as catalysts., Alkoxides are derived from alcohols by the replacement of the hydroxyl hydrogen by metal isopropylate., Metal Alkoxides, General Manufacturing Information: Ethanol, aluminum salt (3:1): ACTIVE, Laboratory procedure: Gattermann-Wieland |
| Category | Inorganic Chemicals |
Documented applications: Uses: Used in reduction of aldehydes and ketones and as a polymerization catalyst, [Merck Index], In reduction of aldehydes and ketones, as catalyst for polymerizations., Catalyst for preprn. of esters from aldehydes and alcoholysis of diketones., Catalyst, with compounds of early transition metals as Ziegler-Natta polymerization catalysts, intermediates in organic syntheses., Aluminum alkyls, Intermediates in organic phosphate insecticides, silicones, special saturated hydrocarbons, terpene alcohols, and organic acids., Aluminum alkyls are used for the preparation of Ziegler-Natta-type catalysts, in the polymerization of olefins, and in the alfen and alfol processes for the production of alpha-olefins and alcohols, respectively., Aluminum Alkyls, Methods of Manufacturing: ...By reacting aluminum powder with absolute ethanol in xylene using small amount of mercuric chloride and iodine as catalysts., Alkoxides are derived from alcohols by the replacement of the hydroxyl hydrogen by metal isopropylate., Metal Alkoxides, General Manufacturing Information: Ethanol, aluminum salt (3:1): ACTIVE, Laboratory procedure: Gattermann-Wieland.
aluminium triethanolate is an inorganic compound with CAS registry number 555-75-9 and molecular formula C6H15AlO3 (molecular weight 162.16), belonging to the inorganic chemicals segment of chemical raw materials.
CAS number: 555-75-9
Its molecular formula C6H15AlO3 comprises 6 C, 15 H, 1 Al, 3 O atoms.
Also known as: aluminium triethanolate · 三乙醇铝
Category: inorganic chemicals
The CAS registry number of aluminium triethanolate is 555-75-9.
Molecular formula C6H15AlO3, molecular weight 162.16.
It is also registered under: aluminium triethanolate, 三乙醇铝.
Recorded applications: Uses: Used in reduction of aldehydes and ketones and as a polymerization catalyst, [Merck Index], In reduction of aldehydes and ketones, as catalyst for polymerizations., Catalyst for preprn. of esters from aldehydes and alcoholysis of diketones., Catalyst, with compounds of early transition metals as Ziegler-Natta polymerization catalysts, intermediates in organic syntheses., Aluminum alkyls, Intermediates in organic phosphate insecticides, silicones, special saturated hydrocarbons, terpene alcohols, and organic acids., Aluminum alkyls are used for the preparation of Ziegler-Natta-type catalysts, in the polymerization of olefins, and in the alfen and alfol processes for the production of alpha-olefins and alcohols, respectively., Aluminum Alkyls, Methods of Manufacturing: ...By reacting aluminum powder with absolute ethanol in xylene using small amount of mercuric chloride and iodine as catalysts., Alkoxides are derived from alcohols by the replacement of the hydroxyl hydrogen by metal isopropylate., Metal Alkoxides, General Manufacturing Information: Ethanol, aluminum salt (3:1): ACTIVE, Laboratory procedure: Gattermann-Wieland.
Category: Inorganic Chemicals.
Independent reference data for aluminium triethanolate (CAS 555-75-9), compiled from public chemistry databases.
| CAS Registry Number | 555-75-9 |
|---|---|
| PubChem CID | 11153 |
| Molecular formula | C6H15AlO3 |
| IUPAC name | aluminum ethanolate |
| UNII (FDA) | S34F5V33DX |
| Molecular Weight | 162.16 |
|---|---|
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 162.0836577 |
| Monoisotopic Mass | 162.0836577 |
| Topological Polar Surface Area | 69.2 |
| Heavy Atom Count | 10 |
| Boiling Point | 200 °C @ 6-8 mm Hg; 175-180 °C @ 3 mm Hg |
|---|---|
| Density | 1.142 @ 20 °C / 0 °C |
Aluminum ethoxide; 555-75-9; Ethanol, aluminum salt; Triethoxyaluminum; ALUMINUM ETHYLATE; Aluminium triethanolate; aluminum ethanolate; Ethyl alcohol, aluminum salt; aluminum triethylate; S34F5V33DX; Ethanol, aluminum salt (3:1); HSDB 5430; EINECS 209-105-8; ALUMINUM ETHOXIDE [MI]; TRIS(ETHANOLATO)ALUMINUM; DTXSID7027203
| GHS notification summary | 9.4% (5 / 53) |
|---|
| GHS notification summary | 9.4% (5 / 53) |
|---|---|
| Reported hazard statements | H228 (90.6%), H314 (90.6%) |
This chemical does not meet GHS hazard criteria for 9.4% (5 of 53) of reports.
H228 (90.6%): Flammable solid [Danger Flammable solids]
aluminium triethanolate · CAS 555-75-9 · C6H15AlO3. UNII S34F5V33DX. Boiling Point: 200 °C @ 6-8 mm Hg; 175-180 °C @ 3 mm Hg; Density: 1.142 @ 20 °C / 0 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 三乙醇铝