2,6-Dihydroxybenzoic acid
[CAS# 303-07-1]

Identification

• Classification: Chemical reagent >> Organic reagent >> Aromatic acid
• Name: 2,6-Dihydroxybenzoic acid
• Synonyms: 2,6-Resorcylic acid; gamma-Resorcylic acid
• Molecular Formula: C₇H₆O₄
• Molecular Weight: 154.12
• CAS Registry Number: 303-07-1
• EC Number: 206-134-8
• SMILES: C1=CC(=C(C(=C1)O)C(=O)O)O

Properties

• Density: 1.6±0.1 g/cm³, Calc.^*
• Melting point: 165 ºC (decomp.)
• Index of Refraction: 1.671, Calc.^*
• Boiling Point: 343.7±32.0 ºC (760 mmHg), Calc.^*
• Flash Point: 175.8±21.6 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H315-H319-H335
• Precautionary Statements: P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Eye irritation	Eye Irrit.	2	H319
Skin irritation	Skin Irrit.	2	H315
Specific target organ toxicity - single exposure	STOT SE	3	H335

Discovory and Applicatios

2,6-Dihydroxybenzoic acid, also known as salicylic acid or 2,6-dihydroxybenzenecarboxylic acid, is an organic compound with the molecular formula C7H6O4. This compound is a derivative of benzoic acid, characterized by the presence of two hydroxyl groups located at the 2 and 6 positions of the aromatic ring. The discovery of 2,6-dihydroxybenzoic acid dates back to the late 19th century when it was first isolated from the bark of willow trees (Salix species). Its historical significance is attributed to its association with the analgesic and anti-inflammatory properties of salicylates, which led to the development of aspirin (acetylsalicylic acid).

The applications of 2,6-dihydroxybenzoic acid are extensive, particularly in the fields of medicine, agriculture, and analytical chemistry. One of its most notable uses is in the pharmaceutical industry, where it serves as a precursor for the synthesis of various salicylate derivatives. These compounds are well-known for their anti-inflammatory, analgesic, and antipyretic properties. Salicylic acid itself is commonly used in the formulation of topical treatments for acne and psoriasis, as it helps to exfoliate the skin and reduce inflammation.

In agriculture, 2,6-dihydroxybenzoic acid has been identified as a plant growth regulator. It plays a role in enhancing plant resistance to environmental stress, such as drought and disease. Its application as a biostimulant promotes root development and overall plant vigor, making it valuable in sustainable agriculture practices. Researchers have explored its potential in improving crop yields and enhancing the nutritional quality of various food crops.

Moreover, 2,6-dihydroxybenzoic acid is utilized in analytical chemistry, particularly in the development of various analytical methods for detecting metal ions. It can form stable complexes with certain metal ions, facilitating their determination in environmental samples. The compound has been employed in spectrophotometric methods for the analysis of heavy metals, contributing to environmental monitoring efforts.

The synthesis of 2,6-dihydroxybenzoic acid typically involves the hydroxylation of benzoic acid or the oxidation of 2,6-dihydroxybenzaldehyde. These synthetic routes are straightforward and allow for the efficient production of the compound for research and industrial applications.

In summary, 2,6-dihydroxybenzoic acid is a compound of significant interest due to its diverse applications in medicine, agriculture, and analytical chemistry. Its historical importance, stemming from its association with salicylates and their therapeutic effects, continues to be relevant today. Ongoing research into its properties and potential uses may lead to further advancements in various fields, particularly in the development of sustainable agricultural practices and novel therapeutic agents.