619-05-6 | 3,4-Diaminobenzoic acid

Packsize	Purity	Availability	Price	Discounted Price
10g	90%	in stock	$7.00	$5.00
25g	90%	in stock	$9.00	$7.00
100g	90%	in stock	$31.00	$22.00
500g	90%	in stock	$93.00	$65.00

Description

• Catalog Number: AB63652
• Chemical Name: 3,4-Diaminobenzoic acid
• CAS Number: 619-05-6
• Molecular Formula: C7H8N2O2
• Molecular Weight: 152.15062
• MDL Number: MFCD00007726
• SMILES: OC(=O)c1ccc(c(c1)N)N

Computed Properties

• Complexity: 161
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 0.2

Upstream Synthesis Route

3,4-Diaminobenzoic Acid, also known as DABA, is a versatile organic compound that finds significant application in chemical synthesis. In the realm of organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, dyes, and polymers. One of the primary uses of 3,4-Diaminobenzoic Acid is in the production of dyes and pigments. Its chemical structure allows it to participate in multiple reactions, leading to the formation of vibrant and stable colored compounds. Additionally, DABA is employed in the synthesis of pharmaceuticals, particularly as a precursor in creating certain antibiotics and antifungal agents. Furthermore, 3,4-Diaminobenzoic Acid plays a crucial role in the development of polymeric materials. Through its reactivity with other compounds, it can be incorporated into polymer chains to impart specific properties such as enhanced strength, flexibility, or thermal stability. Overall, the versatility of this compound in chemical synthesis makes it a valuable tool for researchers and manufacturers across various industries.

Literature

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  Chembiochem : a European journal of chemical biology 20111104

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  Dalton transactions (Cambridge, England : 2003) 20100507

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• Vibrational spectra and quantum chemical calculations of 3,4-diaminobenzoic acid.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080701

• (99m)Tc complexes with activated ester functions; ligands comprising a 3,4-diamino-benzoate backbone.

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• On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines.

  Organic & biomolecular chemistry 20031207

• Reducing the alkali cation adductions of oligonucleotides using sol-gel-assisted laser desorption/ionization mass spectrometry.

  Analytical chemistry 20030815