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Tris-(2-carbamimidoylmercapto-ethyl)-amine; tetrahydrochloride is a complex organic compound with the chemical formula C9H24Cl4N6S3. It is a derivative of tris(2-carboxyethyl)phosphine (TCEP), where the phosphorus atom is replaced by a nitrogen atom and the carboxylic acid groups are replaced by carbamimidoylmercapto groups. tris-(2-carbamimidoylmercapto-ethyl)-amine; tetrahydrochloride is known for its ability to act as a reducing agent, similar to TCEP, but with a different mechanism due to the presence of the nitrogen and sulfur atoms. It is often used in biochemical research and applications where selective reduction of disulfide bonds is required, such as in the study of proteins and their folding. The tetrahydrochloride salt form of the compound enhances its solubility in aqueous solutions, which is beneficial for its use in various biological assays and reactions.

95458-66-5

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95458-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95458-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,4,5 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95458-66:
(7*9)+(6*5)+(5*4)+(4*5)+(3*8)+(2*6)+(1*6)=175
175 % 10 = 5
So 95458-66-5 is a valid CAS Registry Number.

95458-66-5Downstream Products

95458-66-5Relevant academic research and scientific papers

A unique aliphatic tertiary amine chromophore: Fluorescence, polymer structure, and application in cell imaging

Sun, Miao,Hong, Chun-Yan,Pan, Cai-Yuan

, p. 20581 - 20584 (2012)

Although photoluminescence of tertiary aliphatic amines has been extensively studied, the usage of this fundamental chromophore as a fluorescent probe for various applications has unfortunately not been realized because their uncommon fluorescence is easily quenched, and strong fluorescence has been observed only in vapor phase. The objective of this study is how to retain the strong fluorescence of tertiary amines in polymers. Tertiary amines as branching units of the hyperbranched poly(amine-ester) (HypET) display relatively strong fluorescence (Φ = 0.11-0.43). The linear polymers with tertiary amines in the backbone or as the side group are only very weakly fluorescent. The tertiary amine of HypET is easily oxidized under ambient conditions, and red-shifting of fluorescence for the oxidized products has been observed. The galactopyranose-modified HypET exhibits low cytotoxicity and bright cell imaging. Thus, this study opens a new route of synthesizing fluorescent materials for cell imaging, biosensing, and drug delivery.

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