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(4-carboxybutyl)trimethylammonium bromide, also known as CTAB, is a quaternary ammonium salt that is commonly used as a surfactant in various chemical and biological applications. It is derived from the quaternization of trimethylamine with 4-carboxybutyl bromide, resulting in a positively charged nitrogen atom with three methyl groups and a carboxybutyl group.

66258-96-6

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66258-96-6 Usage

Uses

Used in Molecular Biology and Biochemistry:
CTAB is used as a surfactant for solubilizing proteins and lipids, aiding in the study and manipulation of these biomolecules in research and laboratory settings.
Used in Nanoparticle Synthesis:
CTAB is used as a cationic stabilizer in the synthesis of nanoparticles, contributing to the formation and stabilization of these particles for various applications.
Used in Emulsion Polymerization:
CTAB is used as a cationic stabilizer in emulsion polymerization, helping to control the size and distribution of polymer particles during the process.
Used in Nucleic Acid Sample Preparation:
CTAB is used in the preparation of DNA, RNA, and other nucleic acid samples due to its ability to bind and release DNA from silica surfaces, facilitating the isolation and purification of these genetic materials.
Used in Pharmaceutical and Cosmetic Industries:
CTAB is used for its antimicrobial and preservative properties, helping to maintain the safety and shelf life of products in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 66258-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,5 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66258-96:
(7*6)+(6*6)+(5*2)+(4*5)+(3*8)+(2*9)+(1*6)=156
156 % 10 = 6
So 66258-96-6 is a valid CAS Registry Number.

66258-96-6Downstream Products

66258-96-6Relevant academic research and scientific papers

Comparison of the substrate selectivity and biochemical properties of human and bacterial γ-butyrobetaine hydroxylase

Rydzik, Anna M.,Leung, Ivanhoe K.H.,Kochan, Grazyna T.,Loik, Nikita D.,Henry, Luc,McDonough, Michael A.,Claridge, Timothy D.W.,Schofield, Christopher J.

supporting information, p. 6354 - 6358 (2014/08/18)

2-Oxoglutarate and iron dependent oxygenases have potential for the stereoselective hydroxylation of amino acids and related compounds. The biochemical and kinetic properties of recombinant γ-butyrobetaine hydroxylase from human and Pseudomonas sp. AK1 we

Targeting carnitine biosynthesis: Discovery of new inhibitors against γ-butyrobetaine hydroxylase

Tars, Kaspars,Leitans, Janis,Kazaks, Andris,Zelencova, Diana,Liepinsh, Edgars,Kuka, Janis,Makrecka, Marina,Lola, Daina,Andrianovs, Viktors,Gustina, Daina,Grinberga, Solveiga,Liepinsh, Edvards,Kalvinsh, Ivars,Dambrova, Maija,Loza, Einars,Pugovics, Osvalds

, p. 2213 - 2236 (2014/04/17)

γ-Butyrobetaine hydroxylase (BBOX) catalyzes the conversion of gamma butyrobetaine (GBB) to l-carnitine, which is involved in the generation of metabolic energy from long-chain fatty acids. BBOX inhibitor 3-(1,1,1-trimethylhydrazin-1-ium-2-yl)propanoate (

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