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1,3,5-Benzenetriamine, 2,4,6-trimethyl-, trihydrochloride is a chemical compound characterized by a benzene ring with three methylated amine groups and three chloride ions. This trihydrochloride salt form enhances its solubility in water, making it easier to handle in various applications.

100306-38-5

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100306-38-5 Usage

Uses

Used in Organic Synthesis:
1,3,5-Benzenetriamine, 2,4,6-trimethyl-, trihydrochloride is used as a reagent in the production of pharmaceuticals, dyes, and polymers due to its versatile chemical structure and reactivity.
Used in Corrosion Inhibition:
1,3,5-Benzenetriamine, 2,4,6-trimethyl-, trihydrochloride is used as a corrosion inhibitor to protect metal surfaces from degradation, offering a practical solution in various industries where metal corrosion is a concern.
Used in Metal Ion Extraction:
1,3,5-Benzenetriamine, 2,4,6-trimethyl-, trihydrochloride is used as a chelating agent in metal ion extraction processes, facilitating the separation and recovery of metal ions from various sources.
It is important to handle 1,3,5-Benzenetriamine, 2,4,6-trimethyl-, trihydrochloride with care due to its potential health hazards and environmental impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 100306-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,0 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100306-38:
(8*1)+(7*0)+(6*0)+(5*3)+(4*0)+(3*6)+(2*3)+(1*8)=55
55 % 10 = 5
So 100306-38-5 is a valid CAS Registry Number.

100306-38-5Upstream product

100306-38-5Downstream Products

100306-38-5Relevant academic research and scientific papers

1-Azaadamantanes from Substituted Phloroglucinols

Risch, Nikolaus

, p. 4849 - 4856 (2007/10/02)

The heterocycles 3 are synthesised from substituted phloroglucinols 2 and hexamethylenetetramine in one step.Special chemical properties of these 1-azaadamantanes are, for example, the formation of a BH3-complex 4 and the stereoselective reduction to the trialcohol 6.The reaction of 6 with trimethoxymethane yields the heterodiamantane.

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