CAS 19806-17-8

1,3-Phenylenediacetic acid

Description:

1,3-Phenylenediacetic acid, with the CAS number 19806-17-8, is an organic compound characterized by its structure, which features two carboxylic acid groups (-COOH) attached to a phenylene ring. This compound is typically a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid functional groups. It exhibits properties typical of dicarboxylic acids, including the ability to form esters and amides through reactions with alcohols and amines, respectively. The compound is of interest in various fields, including organic synthesis and materials science, due to its potential applications in the development of polymers and pharmaceuticals. Additionally, its structural features may contribute to its reactivity and interactions in biological systems. Safety data indicates that, like many organic acids, it should be handled with care to avoid irritation to skin and eyes.

Formula: C₁₀H₁₀O₄

InChI: InChI=1/C10H10O4/c11-9(12)5-7-2-1-3-8(4-7)6-10(13)14/h1-4H,5-6H2,(H,11,12)(H,13,14)/p-2

InChI key: InChIKey=GDYYIJNDPMFMTB-UHFFFAOYSA-N

SMILES: C(C(O)=O)C1=CC(CC(O)=O)=CC=C1

Synonyms:

• (3-Carboxymethylphenyl)acetic acid
• 1,3-Benzenediacetic acid
• 1,3-Bis-(carboxymethyl)-benzene
• 2,2'-Benzene-1,2-Diyldiacetic Acid
• 2,2'-Benzene-1,3-Diyldiacetate
• 2,2'-Benzene-1,3-Diyldiacetic Acid
• 2,2′-(1,3-Phenylene)diacetic acid
• 2-[3-(Carboxymethyl)phenyl]acetic acid
• Benzene-1,3-diacetic acid
• NSC 75867
• m-Benzenediacetic acid
• m-Phenylendiacetic acid
• m-Phenylenediacetic acid
• 1,3-Phenylenediacetic acid
• RARECHEM AL BO 0129
• 2,2’-(m-phenylene)di-aceticaci
• 1,3-Phenylenebisacetic acid
• m-Phenylendiacetic acid, 97+%
• 2,2'-(m-phenylene)di-acetic acid
• 1,3-Benzenebis(acetic acid)

1,3-Phenylenediacetic Acid

CAS: 19806-17-8

Formula: C₁₀H₁₀O₄

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 194.19

Ref: 3B-P1064

1,3-Phenylenediacetic acid, 97%

CAS: 19806-17-8

In order to establish defined biomacromolecular systems for mineralised tissue applications, type I collagen was functionalised with 1,3-phenylenediacetic acid (Ph) and investigated at the molecular, macroscopic and functional levels. The solvothermal reactions of 1,2-bis(imidazol-1?-yl)ethane (bime

Formula: C₁₀H₁₀O₄

Purity: 97%

Color and Shape: Crystals and/or powder, White to cream

Molecular weight: 194.19

Ref: 02-A11429

1,3-Benzenediacetic acid

CAS: 19806-17-8

Formula: C₁₀H₁₀O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 194.1840

Ref: IN-DA002B9T

1,3-Phenylenediacetic acid

CAS: 19806-17-8

1,3-Phenylenediacetic acid

Purity: 95%

Molecular weight: 194.18g/mol

Ref: 54-OR350319

m-Phenylenediacetic acid

CAS: 19806-17-8

m-Phenylenediacetic acid is a bioactive chemical.

Formula: C₁₀H₁₀O₄

Purity: 98%

Color and Shape: White To Light Yellow Fine Crystalline Powder

Molecular weight: 194.19

Ref: TM-T21139

2,2′-(1,3-Phenylene)diacetic acid

CAS: 19806-17-8

Formula: C₁₀H₁₀O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 194.186

Ref: 10-F223907

1,3-Phenylenediacetic acid

CAS: 19806-17-8

1,3-Phenylenediacetic acid is a molecule that contains an aromatic ring and two carboxylate groups. It has been shown to react with collagen and water molecules by forming hydrogen bonds. 1,3-Phenylenediacetic acid also reacts with the hydroxyl group in the cell culture media to form a crosslink between two molecules. This reaction was found to be responsible for the observed increase in stiffness of collagen gels. The vibrational and macroscopic analysis of 1,3-phenylenediacetic acid has also revealed that it adopts a tetranuclear structure at room temperature.

Formula: C₁₀H₁₀O₄

Purity: Min. 95%

Molecular weight: 194.18 g/mol

Ref: 3D-FP67466