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1-Hydroxybenzene-2,4,6-tricarboxylic acid, also known as gallic acid, is a naturally occurring organic compound with the chemical formula C7H6O5. It is a polyhydroxybenzoic acid, characterized by its hydroxyl groups at the 1st position and three carboxylic acid groups at the 2nd, 4th, and 6th positions on the benzene ring. Gallic acid is widely found in plants, particularly in gallnuts, sumac, witch hazel, and tea leaves. It is known for its antioxidant, anti-inflammatory, and antimicrobial properties, and is used in various applications, including food preservation, pharmaceuticals, and cosmetics. Additionally, gallic acid serves as a precursor in the synthesis of other compounds, such as gallates, which are used as antioxidants in industrial applications.

609-98-3

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609-98-3 Usage

Derivative of hydroxybenzoic acid

Yes, it is a derivative of the phenolic compound hydroxybenzoic acid.

Number of carboxylic acid functional groups

Three, it is characterized by its three carboxylic acid functional groups.

Common uses

Production of pharmaceuticals, agrochemicals, and as a chelating agent in metal ion removal processes.

Potential properties

Antioxidant and anti-inflammatory properties.

Potential treatment for diseases

Metabolic disorders and oxidative stress-related illnesses.

Check Digit Verification of cas no

The CAS Registry Mumber 609-98-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 609-98:
(5*6)+(4*0)+(3*9)+(2*9)+(1*8)=83
83 % 10 = 3
So 609-98-3 is a valid CAS Registry Number.

609-98-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxybenzene-1,3,5-tricarboxylic acid

1.2 Other means of identification

Product number -
Other names 1,3,5-Benzenetricarboxylic acid, 2-hydroxy-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:609-98-3 SDS

609-98-3Relevant academic research and scientific papers

A transmitting near-infrared fluorescent organically accepts line and its preparation method

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Paragraph 0026-0028, (2017/08/25)

The invention relates to a near infrared fluorescence-emission organic nano-wire and a preparation method thereof. The organic nano-wire comprises 2, 4, 6-TBTP. The preparation method comprises that p-hydroxybenzoic acid and urotropine undergo a backflow reaction in trifluoroacetic acid at a temperature of 105-115 DEG C, the reaction product is cooled to a room temperature, the cooled reaction product is poured into water, the solution is filtered, the filtered product and 2-aminothiophenol undergo a backflow reaction in dimethylsulfoxide at a temperature of 175-185 DEG C, the reaction product is cooled to a room temperature, the cooled reaction product is poured into water, the solution is filtered and purified to form 2, 4, 6-TBTP, the 2, 4, 6-TBTP is dissolved in chloroform, and the solution is natural and completely volatilized in a fuming cupboard at a room temperature. The preparation method has simple processes. The near infrared fluorescence-emission organic nano-wire has solid fluorescence emission wavelength of 500-750nm in a near infrared zone, a Stokes shift of 200nm or more, a high fluorescence emission quantum yield and an important application prospect in development of an organic near infrared luminescent material.

AROMATIC TRIAMIDE-LANTHANIDE COMPLEXES

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Page/Page column 84-85, (2008/06/13)

The present invention provides luminescent lanthanide metal chelates comprising a metal ion of the lanthanide series and a complexing agent comprising at least one phthalamidyl moiety. Also provided are probes incorporating the phthalamidyl ligands of the invention and methods utilizing the ligands of the invention and probes comprising the ligands of the invention.

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