89-42-9 Usage
Structure
sulfonated derivative of 2-aminobenzoic acid
The compound is derived from 2-aminobenzoic acid by introducing a sulfonic acid group (-SO3H), which modifies its properties and applications.
Methylamino group
at the 2-position of the benzene ring
The compound contains a methylamino group (-NHCH3) attached to the 2nd carbon position on the benzene ring, which influences its reactivity and solubility.
Use as a fluorescent labeling reagent
in biochemistry and biotechnology applications
2-(methylamino)-5-sulphobenzoic acid is commonly used to label biomolecules, such as proteins, for detection and quantification purposes in various scientific studies.
Applications in medical imaging and drug delivery systems
potential uses
The compound has been researched for its possible applications in medical imaging techniques and as a component in drug delivery systems due to its unique properties.
Increased water solubility
due to sulphonation of the benzene ring
The presence of the sulfonic acid group (-SO3H) in the compound enhances its solubility in water, making it more suitable for use in aqueous solutions and biological assays.
Check Digit Verification of cas no
The CAS Registry Mumber 89-42-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89-42:
(4*8)+(3*9)+(2*4)+(1*2)=69
69 % 10 = 9
So 89-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO5S/c1-9-7-3-2-5(15(12,13)14)4-6(7)8(10)11/h2-4,9H,1H3,(H,10,11)(H,12,13,14)
