N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine Basic Product Information

Product Name	N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine	CAS	2372-82-9
Synonyms	1,3-Propanediamine,N1-(3-aminopropyl)-N1-dodecyl-;1,3-Propanediamine,N-(3-aminopropyl)-N-dodecyl- (9CI);Dodecylamine, N,N-bis(3-aminopropyl)-(6CI,7CI,8CI);Lonzabac 12;Lonzabac 12.100;Lonzabac 1230;N,N-Bis(3-aminopropyl)dodecylamine;N,N-Bis(3-aminopropyl)laurylamine;RC 5637;Triameen Y 12;	Molecular Formula	C18H41N3
EINECS Number	219-145-8	Molecular Structure
Appearance	Light Yellow Powder
Purity	95.00%
Supply Ability

N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine Quality documents

N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine Application

N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine literature

RESIN COMPOSITION AND MOLDED PRODUCT OBTAINED BY MOLDING THE RESIN COMPOSITION

-

, (2010/04/23)

Provided are a resin composition comprising 100 parts by mass of the polymer having an alicyclic structure at least in a part of a repeating structural unit and 0.05 to 5 parts by mass of a hindered amine compound having a carbon atom at a ratio of from 67% by weight to 80% by weight in the molecular structure and having a molecular weight of from 500 to 3500, a novel piperidine derivative having a piperidylaminotriazine skeleton, a molded product such as an optical component obtained by molding the resin composition, and an optical pickup device which employs the optical component.

Preparation of N-alkylbis(3-aminopropyl)amines by the catalytic hydrogenation of N-alkylbis(cyanoethyl)amines

Denton, Travis T.,Joyce, Abigail S.,Kiely, Donald E.

, p. 4997 - 5000 (2008/02/05)

(Chemical Equation Presented) An improved process for the preparation of N-alkylbis(3-aminopropyl)amines is described. These triamines are of interest as monomers for the condensation polymerization with esterified carbohydrate diacids (aldaric acids) to generate the corresponding poly(4-alkyl-4- azaheptamethylene aldaramides). The triamine synthesis is comprised of two efficient steps and requires no chromatographic purification. Bisconjugate addition of alkylamines to acrylonitrile followed by catalytic hydrogenation of the N-alkylbis(cyanoethyl)amines over Raney nickel yields the target N-alkylbis(3-aminopropyl)amines. Much less solvent was used in the bisconjugate addition step then previously reported, and in the second step, a relatively low-pressure catalytic hydrogenation (50 psi of hydrogen) was employed using Raney nickel as the catalyst in a 7 N methanolic ammonia solvent system to afford the N-alkylbis(3-aminopropyl)amines of high purity in nearly quantitative yield.

Triamine-trioxides, a process for their preparation, and cleaning agents containing these compounds

-

, (2008/06/13)

Triamine-trioxides of the formula STR1 in which R denotes a saturated or an olefinically unsaturated hydrocarbon radical which has 1 to 3 double bonds and 8 to 22 carbon atoms, n¹ and n² represent an integer from 2 to 3, and n¹ and n² can be identical or different, and a, b, c and d, which are identical or different, each is a number from 1 to 5, with the proviso that the sum (a+b+c+d) should be at most 10. The compounds are prepared from primary amines of the formula RNH₂ by dicyanoalkylation, hydrogenation, ethoxylation and oxidation with hydrogen peroxide. They are suitable for formulating industrial and also cosmetic cleaning agents.

Bis-betaine-amine oxides, process for their preparation, and cleaning agents containing them

-

, (2008/06/13)

Bis-betaine-amine oxides of the formula STR1 in which R is a saturated or an olefinically unsaturated hydrocarbon radical having 1 to 3 double bonds and 8 to 22 carbon atoms, n¹ and n² each is an integer of from 2 to 3, n¹ and n² optionally being identical or different, m¹ and m² each is an integer of from 1 to 4, m¹ and m² optionally being identical or different, and a, b, c and d, being identical or different, each is a number of from 1 to 5, with the proviso that the sum (a+b+c+d) is at most 10. The compounds are prepared from primary amines of the formula RNH₂, by dicyanoalkylation, hydrogenation, ethoxylation, reaction with alkali metal salts of ω-halocarboxylic acids, and subsequent oxidation with hydrogen peroxide. They are surfactants of mild action and suitable for formulating cosmetic and industrial cleaning agents.

N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine Upstream and downstream

2372-82-9 Upstream product

• 1555-62-0

  N-dodecyl-2,2'-iminodipropionitrile 

• 124-22-1

  n-Dodecylamine 

• 107-13-1

  acrylonitrile 

• 123-91-1

  1,4-dioxane 

2372-82-9 Downstream Products

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