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Benzenemethanaminium, N-[2-(dodecyloxy)-2-oxoethyl]-N,N-dimethyl-, chloride is a complex organic compound with the chemical formula C21H38ClNO3. It is a derivative of benzenemethanaminium, featuring a dodecyloxy group attached to the ethyl chain, which is connected to the nitrogen atom. Benzenemethanaminium, N-[2-(dodecyloxy)-2-oxoethyl]-N,N-dimethyl-, chloride is characterized by its cationic nature, making it a potential surfactant or a component in various chemical formulations. Its structure includes a benzene ring, an amino group, and a quaternary ammonium center, which contributes to its reactivity and solubility properties. The chloride ion associated with it suggests that it may be used in reactions where a counterion is necessary to balance the charge. Benzenemethanaminium, N-[2-(dodecyloxy)-2-oxoethyl]-N,N-dimethyl-, chloride has applications in the fields of chemistry and material science, particularly in the synthesis of surfactants, detergents, and other specialty chemicals.

87297-97-0

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87297-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87297-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,9 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87297-97:
(7*8)+(6*7)+(5*2)+(4*9)+(3*7)+(2*9)+(1*7)=190
190 % 10 = 0
So 87297-97-0 is a valid CAS Registry Number.

87297-97-0Downstream Products

87297-97-0Relevant academic research and scientific papers

Synthesis of some acyclic quaternary ammonium compounds. Alkylation of secondary and tertiary amines in a two-phase system

Kharlamov,Artyushin,Bondarenko

, p. 2445 - 2454 (2015/08/03)

A series of acyclic symmetrical and asymmetrical quaternary ammonium chlorides of the general formula R1R2R3N+AR4Cl- (R1 = Me, Bu; R2 = n-C12H25, PhCH2, C n H2n+1(OCH2CH2) m, n = 9 and 12, m = 1 and 2; R3 = n-C12H25, PhCH2, HOCH2CH2,-OOCCH2; R4 = n-C12H25, PhCH2; A = (CH2CH2O)1,2, CH2C(O)O) was synthesized by the alkylation of tertiary amines in a two-phase system containing water. A convenient method for the synthesis of the initial symmetrical and asymmetrical tertiary amines of the general formula MeNR1R2 (R1 = Me, Bu; R2 = n-C12H25, PhCH2, CnH2n+1(OCH2CH2) m, n = 9 and 12, m = 1 and 2) in an organic phase-aqueous phase heterogeneous system, which allows the use of aqueous solutions of alkali and amines, was developed. The improved method for the preparation of intermediate ethylene glycol and diethylene glycol monoethers is monoalkylation of glycols in dioxane using solid KOH in a two-phase system.

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