where can you use these amines?

Where can you Among the many products for which t-butylamine arid t-octylamine have been suggested as intermediates are rubber chemicals, insecticides, bactericides, oil additives, photographic chemicals, pharmaceuticals, surface active agents, corrosion inhibitors, and dye- stuffs. Perhaps other applications where these amines would prove helpful will occur to you. These t-alkyl primary amines react quite differently, in many respects, from analogous straight-chain primary amines. When reacted with aldehydes, for example, t-butylamine and t-octylamine yield stable, monomeric aldimines (R-N=CHR') ; with cyanogen ROHM & HAAS COMPANY, Washington Square, Phila. 5, Pa. Please send me information and samples on the following: • t-butylamlne and t-octylamine Send me information on the following: • Acrylic Monomers • Alkyl Phenols D PRIMENE Aminos Π Dimefhylformamide D PRIMINOX Polyethoxy Amines Π Methylamines Nam· - Firm Title Address City Stat· Β these amines? chloride, stable, monomeric cyanamides (R-NH-CN) are formed. The t-alkyl primary amines can be alkylated and alkoxylated to produce secondary amines, with very little tertiary amine formation. Like the straigpht-chain primary amines, however, t-butylarnine and t-octylamine are of normal basic strength, and undergo most of the reactions common to the primary amines. Both t-butylamine and t-octylamine are light colored liquids; t-butylamine boils at 44° to 55°C, t-octylamine at 137° to 143°C. They are available in commercial quantities. CHEMICALS E=3=3 FOR INDUSTRY ROHM £- HAAS COMPANY WASHINGTON SQUARE, ΡΗΙΙΑΟΕΙΡΗΓΑ 5, PA. I Rcpmentathvs in principal foreign countries I PRIMENE and PWHIMOX are trademarks, Reg. U.S. Pat. Off. and) in principal foreign countries. - : _··..-'."Λ ·*."·-' Wife W$3 m : <^| m-c-cH„ ^Tf 5 CH 3 cu s tButylarnirie t'ijckvlamihe use

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Where can you Among the many products for which t-butyl-amine arid t-octylamine have been suggested as intermediates are rubber chemicals, insecticides, bactericides, oil additives, photographic chemicals, pharmaceuticals, surface active agents, corrosion inhibitors, and dye-stuffs. Perhaps other applications where these amines would prove helpful will occur to you. These t-alkyl primary amines react quite differently, in many respects, from analogous straight-chain primary amines. When reacted with aldehydes, for example, t-butyl-amine and t-octylamine yield stable, mono-meric aldimines (R-N=CHR') ; with cyanogen

R O H M & H A A S C O M P A N Y , W a s h i n g t o n S q u a r e , Phi la. 5 , P a .

Please send me in fo rma t i on a n d samples o n t he f o l l o w i n g : • t - b u t y l a m l n e a n d t - o c t y l a m i n e

Send me in fo rmat ion o n the f o l l o w i n g : • Acry l ic M o n o m e r s • A l k y l Phenols D PRIMENE A m i n o s Π D i m e f h y l f o r m a m i d e D P R I M I N O X P o l y e t h o x y A m i n e s Π M e t h y l a m i n e s

Nam· -

Firm Title

Address

City Stat ·

Β these amines? chlor ide , stable, m o n o m e r i c cyanamides (R-NH-CN) are formed. The t-alkyl primary amines can be alkylated and alkoxylated to produce secondary amines, with very little tertiary amine formation.

Like the straigpht-chain primary amines, however, t-butylarnine and t-octylamine are of normal basic strength, and undergo most of the reactions common to the primary amines. Both t-butylamine and t-octylamine are light colored liquids; t-butylamine boils at 44° to 55°C, t-octylamine at 137° to 143°C. They are available i n commercial quantities.

CHEMICALS E = 3 = 3 FOR INDUSTRY

ROHM £- HAAS C O M P A N Y

WASHINGTON SQUARE, ΡΗΙΙΑΟΕΙΡΗΓΑ 5, PA. I Rcpmentathvs in principal foreign countries I

PRIMENE and PWHIMOX are trademarks, Reg. U.S. Pat. Off. and) in principal foreign countries.

-:_··..-'."Λ ·*."·-'

Wife

W$3

m : < ^ | m-c-cH„ ^ T f 5

CH3 cus

tButylarnirie t'ijckvlamihe

use

acides amines