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42823-72-3

4-AMIDINOBENZOIC ACID HCL, also known as p-aminobenzoic acid hydrochloride, is a chemical compound with the molecular formula C7H7ClN2O2. It is a white to off-white crystalline powder that is soluble in water and alcohol. This derivative of para-aminobenzoic acid is widely recognized for its applications in the pharmaceutical industry, as well as for its antifungal and antibacterial properties, making it a valuable ingredient in various products.

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  • 42823-72-3 Structure

  • Basic information

    1. Product Name: 4-AMIDINOBENZOIC ACID HCL
    2. 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)
    3. CAS NO:42823-72-3
    4. Molecular Formula: C8H8N2O2*ClH
    5. Molecular Weight: 200.62
    6. EINECS: N/A
    7. Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;pharmacetical
    8. Mol File: 42823-72-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 366.5 °C at 760 mmHg
    3. Flash Point: 175.4 °C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 5.15E-06mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-AMIDINOBENZOIC ACID HCL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-AMIDINOBENZOIC ACID HCL(42823-72-3)
    12. EPA Substance Registry System: 4-AMIDINOBENZOIC ACID HCL(42823-72-3)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 36/37/38-36-22
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 42823-72-3(Hazardous Substances Data)

42823-72-3 Usage

Uses

Used in Pharmaceutical Industry:
4-AMIDINOBENZOIC ACID HCL is used as an intermediate in the synthesis of various drugs, contributing to the development of new medications that can address a range of health concerns.
Used in Dye Production:
In the dye industry, 4-AMIDINOBENZOIC ACID HCL is utilized for its color-producing properties, playing a role in the creation of a variety of dyes.
Used in Cosmetics:
4-AMIDINOBENZOIC ACID HCL is used as a component in cosmetics due to its ability to enhance the formulation's properties, such as stability and effectiveness.
Used in Sunscreen Formulations:
4-AMIDINOBENZOIC ACID HCL is used as a UV absorber in sunscreens, providing protection against harmful ultraviolet radiation, which is essential for skin health.
Used in Topical Medications:
Leveraging its antifungal and antibacterial properties, 4-AMIDINOBENZOIC ACID HCL is used in topical medications to treat various skin conditions and infections.
It is important to handle and store 4-AMIDINOBENZOIC ACID HCL according to safe laboratory practices and guidelines to minimize the risk of skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 42823-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,2 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42823-72:
(7*4)+(6*2)+(5*8)+(4*2)+(3*3)+(2*7)+(1*2)=113
113 % 10 = 3
So 42823-72-3 is a valid CAS Registry Number.
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

42823-72-3SDS

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 4-AMIDINOBENZOIC ACID HCL

1.2 Other means of identification

Product number -
Other names 4-Carboxybenzamidine HCl

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:42823-72-3 SDS

42823-72-3Relevant articles and documents

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

Nicks, Joshua,Boer, Stephanie A.,White, Nicholas G.,Foster, Jonathan A.

, p. 3322 - 3327 (2021/03/17)

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.

Fibrinogen receptor antagonist and pharmaceutical compositions comprising the same

-

, (2008/06/13)

Compounds of the following general formula (I) and pharmaceutically acceptable salts thereof.

2,3-diaminopropionic acid derivative

-

, (2008/06/13)

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.

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