Quality Chinese Factory Supply High Purity 3,5-di-tert-butylsalicylic acid 19715-19-6 In Stock, Wholesale with Fast Shipping
- Molecular Formula:C15H22O3
- Molecular Weight:250.338
- Appearance/Colour:White Powder
- Vapor Pressure:4.19E-08mmHg at 25°C
- Melting Point:157-165 °C(lit.)
- Refractive Index:1.547
- Boiling Point:335.6 °C at 760 mmHg
- PKA:3.34±0.14(Predicted)
- Flash Point:171 °C
- PSA：57.53000
- Density:1.07 g/cm3
- LogP:3.68540
3,5-di-tert-butylsalicylic acid (Cas 19715-19-6) Usage
|
Chemical Properties
|
White powder
|
|
Uses
|
3,5-di-tert-butylsalicylic acid is an important substance widely used as synthetic materials such as pressure sensitive recording paper, agriculture chemicals, antioxidants and so on. 3,5-di-tert-butylsalicylic acid and its derivatives, both metal salts and complexes, possess interesting triboelectrical properties. They are frequently used as charge control additives in dry xerographic toner at low concentrations to control the charging characteristic of toners.
|
InChI:InChI=1/C15H22O4/c1-14(2,3)9-7-8(13(18)19)11(16)10(12(9)17)15(4,5)6/h7,16-17H,1-6H3,(H,18,19)
19715-19-6 Relevant articles
On the Kolbe-Schmitt synthesis of pharmacologically useful salicylates: Carboxylation of 2,4-di-t-butylphenol and identification and reduction of the formation of 2,2'-dihydroxy-3,3',5,5'-tetra-t- butylbiphenyl in the synthesis of 3,5-di-t-butylsalicylic acid
Chidambaram,Sorenson
, p. 810 - 811 (1991)
The initial yield of 3,5-di-t-butylsalic...
Enantioselective Synthesis of DIANANE, a Novel C2-Symmetric Chiral Diamine for Asymmetric Catalysis
Albrecht Berkessel, Michael Schröder, Christoph A. Sklorz, Stefania Tabanella, Nadine Vogl, Johann Lex, and Jörg M. Neudörfl
, J. Org. Chem. 2004, 69, 9, 3050–3056
Finally, DIANANE (3) was condensed with 2 equiv of 3,5-bis-tert-butylsalicylic aldehyde to afford the DIANANE-salen ligand 2 (Schemes 1 and 3). In the course of the crystallization …
Metal complex-(3,5-di-tert-butyl salicylic acid) method for the preparation of
-
Paragraph 0067; 0068, (2017/02/28)
The invention provides a preparation met...
COMPOUNDS USEFUL FOR THE TREATMENT OF METABOLIC DISORDERS AND SYNTHESIS OF THE SAME
-
Page/Page column 124, (2014/10/18)
The present invention provides compounds...
Convenient and efficient method for the obtainment of ketones from highly hindered aromatic N,N-dimethyl-amides
Jimenez, Claudio A.,Belmar, Julio B.
, p. 2391 - 2397 (2008/02/10)
A simple and efficient procedure to synt...
Urotropin synthesis of 3,5-di-tert-butylsalicylic acid derivatives
Vol'eva,Belostotskaya,Komissarova,Kurkovskaya,Pleshakova,Prokofeva
, p. 1488 - 1491 (2008/09/16)
The stability of 3,5-di-tert-butylsalicy...
19715-19-6 Process route
-
- 124-38-9,18923-20-1
carbon dioxide
-
- 37408-22-3
potassium 2,4-di-tert-butylphenolate
-
- 6390-69-8
3,3',5,5'-tetra(tert-butyl)biphenyl-2,2'-diol
-
- 19715-19-6
3,5-ditertbutyl salicylic acid
Conditions
| Conditions |
Yield |
|
under 43957.6 - 46543.3 Torr;
|
|
-
- 15018-03-8
methyl 3,5‐di‐tert-butyl‐2‐hydroxybenzoate
-
- 19715-19-6
3,5-ditertbutyl salicylic acid
Conditions
| Conditions |
Yield |
|
With water; potassium hydroxide; In methanol; for 1h; Reflux;
|
92% |
|
In methanol; water; for 5h; Heating;
|
80% |
|
With potassium hydroxide; In methanol; for 4h; Heating;
|
75% |
|
With potassium hydroxide; In methanol; water;
|
|
|
With sodium hydroxide; In methanol; at 70 - 90 ℃; for 3h; Reagent/catalyst; Solvent; Temperature;
|
152 g |
19715-19-6 Upstream products
-
124-38-9
carbon dioxide
-
37408-22-3
potassium 2,4-di-tert-butylphenolate
-
15018-03-8
methyl 3,5‐di‐tert-butyl‐2‐hydroxybenzoate
-
119-36-8
methyl salicylate
19715-19-6 Downstream products
-
84352-59-0
4-carbomethoxyphenyl 3,5-di-t-butylsalicylate
-
175650-08-5
benzyl 2-benzyloxy-3,5-di-tert-butylbenzoate
-
25130-85-2
3,5-di-tert-butylsalicylic acid chloride
-
37456-29-4
2,4-di-tert-butyl-6-acetylphenol
