1083-41-6 | Butyl gallate

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$14.00	$10.00
5g	95%	in stock	$28.00	$20.00
25g	95%	in stock	$97.00	$68.00
100g	95%	in stock	$330.00	$231.00

Description

• Catalog Number: AB71658
• Chemical Name: Butyl gallate
• CAS Number: 1083-41-6
• Molecular Formula: C11H14O5
• Molecular Weight: 226.2259
• MDL Number: MFCD00016432
• SMILES: CCCCOC(=O)c1cc(O)c(c(c1)O)O
• NSC Number: 33956

Computed Properties

• Complexity: 218
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 5
• XLogP3: 2.4

Upstream Synthesis Route

Butyl 3,4,5-trihydroxybenzoate, also known as butyl gallate, is a versatile compound widely utilized in chemical synthesis. Its primary application lies in its roles as an antioxidant and stabilizer in various chemical processes. Due to its chemical structure containing multiple hydroxyl groups, butyl gallate effectively scavenges free radicals and inhibits oxidation reactions, making it an ideal candidate for preserving the integrity of sensitive compounds.In chemical synthesis, butyl gallate is commonly employed in the formulation of pharmaceuticals, cosmetics, and food products. By preventing unwanted oxidation and degradation reactions, it helps maintain the quality and shelf life of the final products. Additionally, its antioxidant properties make it a valuable additive in polymers and plastics manufacturing, where it contributes to enhancing the materials' durability and longevity.Moreover, butyl gallate’s ability to chelate metal ions further expands its utility in chemical synthesis. This property allows it to act as a catalyst or inhibitor in various reactions, facilitating the formation of desired products and controlling undesirable byproducts.Overall, Butyl 3,4,5-trihydroxybenzoate plays a crucial role in chemical synthesis by serving as an antioxidant, stabilizer, and chelating agent, contributing to the efficient and controlled production of a wide range of chemical compounds and materials.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Relation between lipophilicity of alkyl gallates and antifungal activity against yeasts and filamentous fungi.

  Bioorganic & medicinal chemistry letters 20090315

• Anti-HSV-1 and anti-HIV-1 activity of gallic acid and pentyl gallate.

  Memorias do Instituto Oswaldo Cruz 20080801

• Identification of chemical compounds from the leaves of Leea indica.

  Acta pharmaceutica (Zagreb, Croatia) 20080601

• An ellagitannin, n-butyl gallate, two aryltetralin lignans, and an unprecedented diterpene ester from Pelargonium reniforme.

  Phytochemistry 20080201

• Comparative cytotoxicity of alkyl gallates on mouse tumor cell lines and isolated rat hepatocytes.

  Comparative biochemistry and physiology. Part A, Molecular & integrative physiology 20070401

• Inhibition of human immunodeficiency viral replication by tannins and related compounds.

  Antiviral research 19920501