CAS 1194-98-5

2,5-Dihydroxybenzaldehyde

Description:

2,5-Dihydroxybenzaldehyde, also known as 2,5-dihydroxy-1-benzaldehyde, is an organic compound characterized by the presence of two hydroxyl (-OH) groups and an aldehyde (-CHO) functional group attached to a benzene ring. Its molecular formula is C7H6O3, and it features a phenolic structure, which contributes to its reactivity and solubility in polar solvents. This compound typically appears as a white to light yellow crystalline solid and has a melting point that varies based on purity and environmental conditions. 2,5-Dihydroxybenzaldehyde is known for its applications in organic synthesis, particularly as an intermediate in the production of various pharmaceuticals and dyes. Additionally, it exhibits antioxidant properties, making it of interest in biochemical research. The compound's reactivity can be attributed to the electron-donating effects of the hydroxyl groups, which enhance its electrophilic character. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled.

Formula: C₇H₆O₃

InChI: InChI=1S/C7H6O3/c8-4-5-3-6(9)1-2-7(5)10/h1-4,9-10H

InChI key: InChIKey=CLFRCXCBWIQVRN-UHFFFAOYSA-N

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

Synonyms:

• Formylhydroquinone
• 2,5-Dihydroxybenzaldehyde
• Gentisaldehyde
• 5-Hydroxysalicylaldehyde
• Benzaldehyde, 2,5-dihydroxy-

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

Formula: C₇H₆O₃

Purity: >98.0%(GC)

Color and Shape: Light yellow to Amber to Dark green powder to crystal

Molecular weight: 138.12

Ref: 3B-D0565

2,5-Dihydroxybenzaldehyde, 98+%

CAS: 1194-98-5

It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The

Formula: C₇H₆O₃

Purity: 98+%

Color and Shape: Yellow to dark green to green to brown, Crystals or powder or crystalline powder

Molecular weight: 138.12

Ref: 02-A15565

2,5-Dihydroxybenzaldehyde, 10mM (in DMSO)

CAS: 1194-98-5

2,5-Dihydroxybenzaldehyde, 10mM (in DMSO)

Formula: C₇H₆O₃

Purity: ≥98%, 10 mM in DMSO

Molecular weight: 138.12

Ref: 54-BUP20005

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

2,5-Dihydroxybenzaldehyde

Formula: C₇H₆O₃

Purity: 98%

Color and Shape: Green Solid-Powder

Molecular weight: 138.12073

Ref: 54-OR1868

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

2,5-Dihydroxybenzaldehyde

Purity: ≥98%

Molecular weight: 138.12g/mol

Ref: 54-BUP18235

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

Formula: C₇H₆O₃

Molecular weight: 138.12

Ref: 7W-GK7304

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

Formula: C₇H₆O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 138.1207

Ref: IN-DA000IP8

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

Formula: C₇H₆O₃

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 138.122

Ref: BP-SBP01230

2,5-Dihydroxybenzaldehyde

Controlled Product

CAS: 1194-98-5

Applications 2,5-Dihydroxybenzaldehyde (cas# 1194-98-5) is a compound useful in organic synthesis.

Formula: C₇H₆O₃

Color and Shape: Neat

Molecular weight: 138.12

Ref: TR-D451005

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

2,5-Dihydroxybenzaldehyde (Gentisaldehyde) has antioxidant activity against Mycobacterium avium subsp.

Formula: C₇H₆O₃

Purity: 99.55% - 99.75%

Color and Shape: Solid

Molecular weight: 138.1207

Ref: TM-TN2730

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

2,5-Dihydroxybenzaldehyde is a compound that can be used as an antioxidant. It is also a precursor for the synthesis of benzalkonium chloride. 2,5-Dihydroxybenzaldehyde reacts with p-hydroxybenzoic acid to form 2,5-dihydroxyphenylacetic acid and benzoic acid. The reaction mechanism of 2,5-dihydroxybenzaldehyde has been studied in detail using hl-60 cells and has been shown to be significant cytotoxicity. The hydroxyl group in this molecule creates a hydrogen bond with the carbonyl group in p-hydroxybenzoic acid and the two react together to form products. This reaction is catalyzed by Michaelis–Menten kinetics and proceeds via an electrochemical detector. Nitrogen atoms are not present in this molecule but do exist in benzalkonium chloride, which is synthesized from 2

Formula: C₇H₆O₃

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 138.12 g/mol

Ref: 3D-FD22101

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

Formula: C₇H₆O₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 138.122

Ref: 10-F318713

2,5-Dihydroxybenzaldehyde

CAS: 1194-98-5

2,5-Dihydroxybenzaldehyde

Formula: C₇H₆O₃

Purity: 98%

Molecular weight: 138.12

Ref: IN-DG4701