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CAS

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105995-43-5

3,5-BIS-AMINOMETHYL-BENZOIC ACID is a bifunctional chemical compound that belongs to the family of aminomethyl benzoic acids. It features a benzene ring with two amino groups attached, which endows it with unique chemical properties and a broad spectrum of applications in various industries.

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  • 105995-43-5 Structure

  • Basic information

    1. Product Name: 3,5-BIS-AMINOMETHYL-BENZOIC ACID
    2. Synonyms: 3,5-BIS-AMINOMETHYL-BENZOIC ACID
    3. CAS NO:105995-43-5
    4. Molecular Formula: C9H12N2O2
    5. Molecular Weight: 180.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105995-43-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 401.9°Cat760mmHg
    3. Flash Point: 196.9°C
    4. Appearance: /
    5. Density: 1.269g/cm3
    6. Vapor Pressure: 3.5E-07mmHg at 25°C
    7. Refractive Index: 1.623
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 3.20±0.10(Predicted)
    11. CAS DataBase Reference: 3,5-BIS-AMINOMETHYL-BENZOIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3,5-BIS-AMINOMETHYL-BENZOIC ACID(105995-43-5)
    13. EPA Substance Registry System: 3,5-BIS-AMINOMETHYL-BENZOIC ACID(105995-43-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 105995-43-5(Hazardous Substances Data)

105995-43-5 Usage

Uses

Used in Pharmaceutical Industry:
3,5-BIS-AMINOMETHYL-BENZOIC ACID is used as an active pharmaceutical ingredient for its potential therapeutic applications, particularly as an antifungal and anti-inflammatory agent. Its unique chemical structure allows it to target specific biological pathways, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Dye Industry:
3,5-BIS-AMINOMETHYL-BENZOIC ACID is used as a key intermediate in the synthesis of various dyes. Its chemical properties enable the creation of dyes with specific color characteristics and stability, making it valuable in the production of textiles, paints, and other colorant applications.
Used in Material Science:
3,5-BIS-AMINOMETHYL-BENZOIC ACID is employed in the development of new materials and polymers due to its unique chemical structure and properties. Its ability to form covalent bonds with other molecules allows for the creation of advanced materials with tailored properties, such as improved mechanical strength, thermal stability, or specific chemical reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 105995-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,9 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105995-43:
(8*1)+(7*0)+(6*5)+(5*9)+(4*9)+(3*5)+(2*4)+(1*3)=145
145 % 10 = 5
So 105995-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H12N2O2/c10-4-6-1-7(5-11)3-8(2-6)9(12)13/h1-3H,4-5,10-11H2,(H,12,13)

105995-43-5SDS

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 3,5-bis(aminomethyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 3,5-Bis-aminomethylbenzoic acid

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:105995-43-5 SDS

105995-43-5Downstream Products

105995-43-5Relevant articles and documents

Bivalent inhibitors of glutathione S-transferase: The effect of spacer length on isozyme selectivity

Maeda, Dean Y.,Mahajan, Sumit S.,Atkins, William M.,Zebala, John A.

, p. 3780 - 3783 (2006)

Glutathione S-transferases (GSTs) are cytosolic enzymes that catalyze the conjugation of glutathione with a variety of exogenous and endogenous electrophiles. High affinity, isozyme-specific inhibitors of GST are required for use as pharmacological tools

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