Detail of > 38668-48-3
- MSDS Download

- CAS Number:
- 38668-48-3
- Name:
Diisopropanol-p-toluidine
- Superlist Name:
- 1,1'-((4-Methylphenyl)imino)bis-2-propanol
- Formula:
- C13H21NO2
- Molecular Structure:

- Synonyms:
- 2-Propanol,1,1'-(p-tolylimino)di- (7CI);2-Propanol,1,1'-[(4-methylphenyl)imino]bis-;N,N-Bis(2-hydroxypropyl)-p-toluidine;
- Molecular Weight:
- 223.31134
- EINECS:
- 254-075-1
- Density:
- 1.086 g/cm3
- Boiling Point:
- 389 °C at 760 mmHg
- Flash Point:
- 198.8 °C
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Reference
- Curable resin compositions
- Curable resin compositions. Honda, Kyoshi (Dainippon Ink and Chemicals, Inc., Japan). Japan. Kokai JP 52030890 8 Mar 1977 Showa, 5 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C08F299-00. APPLICATION: JP 74-87899 31 Jul 1974. DOCUMENT TYPE: Patent CA Section: 36 (Plastics Manufacture and Processing) A curable resin compn. is prepd., contg. acrylate monoesters 20-55, acrylate polyesters 5-30, vinyl compds. (copolmerizable with acrylic compds.) 0-20, unsatd. resins 30-75, and arom. amines (based on 100 parts resin compn.) 0.05-2.0 parts. Thus, a mixt. of Me methacrylate [80-62-6] 40, ethylene glycol dimethacrylate [97-90-5] 8, unsatd. polyesters Polylite ODR 449 [55069-49-3] 52, and N,N-bis(2-hydroxypropyl)-p-toluidine [38668-48-3] 0.1 part was stirred to give a soln. which (20 parts) was mixed with 0.5 part Bz2O2, giving a curable resin compn.
- Primer compositions for coating of floors and walls
- Primer compositions for coating of floors and walls. (Mitsubishi Rayon Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 58204057 A2 28 Nov 1983 Showa, 7 pp. (Japanese). (Japan). 97-90-5 and 80-62-6 are cas registry numbers. These chemicals are also mentioned in this article. CODEN: JKXXAF. CLASS: IC: C09D003-727; C08F299-02. ICA: C08G059-16. APPLICATION: JP 82-88418 25 May 1982. DOCUMENT TYPE: Patent CA Section: 42 (Coatings, Inks, and Related Products) The primer compns. are mixts. of 30-60% b-hydroxy esters and 40-70% unsatd. monomers [contg. >80% Me methacrylate (I)] which contain 0.1-5% paraffins and/or waxes m. >40° and 0.1-5% tertiary amines. The b-hydroxy esters are prepd. by the reaction of a bisphenol A-epichlorohydrin epoxy resin with (meth)acrylic acid and a mixt. of 80-100 mol% C8-20 satd. monocarboxylic acids and 0-20 mol% C8-20 unsatd. monocarboxylic acids. Thus, 2000 parts epoxy resin was dissolved in 975 parts I contg. 5 parts 2,4-dimethyl-6-tert-butylphenol at 70°, mixed with 27 parts Et3N, heated to 80°, mixed with 112 parts methacrylic acid and 130 parts lauric acid during 2 h, stirred 8 h at 80°, mixed with 250 parts I, stirred (68 parts) with 31 parts I, heated to 50°, mixed with small amts. of paraffin and N,N'-di(2-hydroxypropyl)-p-toluidine [38668-48-3], cooled, mixed (100 parts) with 3 parts Bz2O2, and coated on a concrete block to form a coating having good adhesion. .
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