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86423-37-2

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86423-37-2 Usage

Family

Alkylamines

Specific Type

Octylamine with a 3-aminopropyl substituent

Common Uses

Manufacturing of adhesives, sealants, and coatings
Acting as a surfactant in applications requiring foaming properties
Corrosion inhibition
Intermediate in the production of pharmaceuticals and other organic compounds

Physical Properties

Acts as a surfactant
Foaming properties

Safety Precautions

Potential for skin and eye irritation
Use in a well-ventilated area

Handling

Handle with caution due to potential health risks

Check Digit Verification of cas no

The CAS Registry Mumber 86423-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,2 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86423-37:
(7*8)+(6*6)+(5*4)+(4*2)+(3*3)+(2*3)+(1*7)=142
142 % 10 = 2
So 86423-37-2 is a valid CAS Registry Number.

86423-37-2Upstream product

86423-37-2Downstream Products

86423-37-2Relevant articles and documents

Lipophilic vancomycin aglycon dimer with high activity against vancomycin-resistant bacteria

Yarlagadda, Venkateswarlu,Sarkar, Paramita,Manjunath, Goutham B.,Haldar, Jayanta

supporting information, p. 5477 - 5480 (2015/11/18)

Antibiotic-resistant superbugs such as vancomycin-resistant Enterococci (VRE) and Staphylococci have become a major global health hazard. To address this issue, we synthesized vancomycin aglycon dimers to systematically probe the impact of a linker on biological activity. A dimer having a pendant lipophilic moiety in the linker showed ~300-fold more activity than vancomycin against VRE. The high activity of the compound is attributed to its enhanced binding affinity to target peptides which resulted in improved peptidoglycan (cell wall) biosynthesis inhibition. Therefore, our studies suggest that these compounds, prepared by using facile synthetic methodology, can be used to combat vancomycin-resistant bacterial infections.

Bis-betaines, a process for their preparation, and cleaning agents containing these compounds

-

, (2008/06/13)

Bis-betaines 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, m1 and m2 represent an integer from 1 to 4, and m1 and m2 can be identical or different, and a, b, c and d, which are identical or different, each is a number from 1 to 5, but 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 reaction with alkali metal salts of ω-halogenocarboxylic acids. They are suitable for formluating cosmetic and industrial 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.

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