42823-72-3

Basic information

• Product Name: 4-AMIDINOBENZOIC ACID HCL
• Synonyms: 4-CARBOXYBENZAMIDINE HYDROCHLORIDE;4-CARBAMIMIDOYL-BENZOIC ACID HYDROCHLORIDE;4-AMIDINOBENZOIC ACID HCL;4-AMIDINOBENZOIC ACID HYDROCHLORIDE;4-Carboxybenzamidine HCl;Benzoic acid, 4-(aminoiminomethyl)-, hydrochloride (1:1)
• CAS NO: 42823-72-3
• Molecular Formula: C₈H₈N₂O₂*ClH
• Molecular Weight: 200.62
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;pharmacetical
• Mol File: 42823-72-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 366.5 °C at 760 mmHg
• Flash Point: 175.4 °C
• Appearance: /
• Vapor Pressure: 5.15E-06mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 4-AMIDINOBENZOIC ACID HCL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMIDINOBENZOIC ACID HCL(42823-72-3)
• EPA Substance Registry System: 4-AMIDINOBENZOIC ACID HCL(42823-72-3)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-36-22
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 42823-72-3(Hazardous Substances Data)

Usage

General Description

4-AMIDINOBENZOIC ACID HCL, also known as p-aminobenzoic acid hydrochloride, is a chemical compound with the molecular formula C7H7ClN2O2. It is a derivative of para-aminobenzoic acid and is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs. 4-AMIDINOBENZOIC ACID HCL is also used in the production of dyes, cosmetics, and as a UV absorber in sunscreen formulations. It is a white to off-white crystalline powder that is soluble in water and alcohol. 4-AMIDINOBENZOIC ACID HCL has antifungal and antibacterial properties, making it a valuable ingredient in topical medications. 4-AMIDINOBENZOIC ACID HCL should be handled and stored according to safe laboratory practices and guidelines due to its potential for skin and eye irritation.

InChI:InChI=1/C8H8N2O2.ClH/c9-7(10)5-1-3-6(4-2-5)8(11)12;/h1-4H,(H3,9,10)(H,11,12);1H

Upstream product

• 59855-11-7 4-carbamoylbenzamidine hydrochloride 
• 54050-86-1 4-Amidinobenzamide 
• 619-65-8 4-cyanobenzoic Acid 

Downstream Products

• 15535-95-2 4-(aminoiminomethyl)benzoic acid 

Relevant articles and documents

Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks

Hydrogen-bonded organic frameworks (HOFs) are a diverse and tunable class of materials, but their potential as free-standing two-dimensional nanomaterials has yet to be explored. Here we report the self-assembly of two layered hydrogen-bonded frameworks based on strong, charge-assisted hydrogen-bonding between carboxylate and amidinium groups. Ultrasound-assisted liquid exfoliation of both materials readily produces monolayer hydrogen-bonded organic nanosheets (HONs) with micron-sized lateral dimensions. The HONs show remarkable stability and maintain their extended crystallinity and monolayer structures even after being suspended in water at 80 °C for three days. These systems also exhibit efficient fluorescence quenching of an organic dye in organic solvents, superior to the quenching ability of the bulk frameworks. We anticipate that this approach will provide a route towards a diverse new family of molecular two-dimensional materials.

2,3-diaminopropionic acid derivative

The present invention relates to a 2,3-diaminopropionic acid derivative of the formula (1): STR1 or a pharmaceutically acceptable salt thereof. The compounds of the present invention are useful as a platelet aggregation inhibitor, a cancer metastasis inhibitor, a wound healing agent or a bone resorption inhibitor.