Ethyl Gallate

• CAS: 831-61-8
• Catalog Number: ACM831618
• Category: Inhibitors
• Molecular Weight: 198.2
• Molecular Formula: C9H10O5
• Description: Ethyl gallate is a nonflavonoid phenolic compound and also a scavenger of hydrogen peroxide.
• Synonyms: Benzoic acid, 3,4,5-trihydroxy-, ethyl ester;Ethyl 3,4,5-trihydroxybenzoate;Gallic acid, ethyl ester
• IUPAC Name: ethyl 3,4,5-trihydroxybenzoate
• Canonical SMILES: CCOC(=O)C1=CC(=C(C(=C1)O)O)O
• InChI: InChI=1S/C9H10O5/c1-2-14-9(13)5-3-6(10)8(12)7(11)4-5/h3-4,10-12H,2H2,1H3
• InChI Key: VFPFQHQNJCMNBZ-UHFFFAOYSA-N
• Appearance: White powder
• Storage: Powder-20°C, 3 years; 4°C, 2 years; In solvent-80°C, 6 months; -20°C, 1 month.
• Active Content: 95%
• Physical State: Solid
• Shipping: Can be shipped at room temperature, where not in use may vary.
• Source: PlantsPaeoniaceaePaeonia lactiflora Pall.

Custom Q&A

What is the IUPAC name of the compound with CAS number 831-61-8?

The IUPAC name of the compound with CAS number 831-61-8 is ethyl 3,4,5-trihydroxybenzoate.

What is the molecular weight of Ethyl Gallate?

The molecular weight of Ethyl Gallate is 198.2.

What is the molecular formula of Ethyl Gallate?

The molecular formula of Ethyl Gallate is C9H10O5.

What is the SMILES notation for Ethyl Gallate?

The SMILES notation for Ethyl Gallate is CCOC(=O)C1=CC(=C(C(=C1)O)O)O.

What is the InChI Key for Ethyl Gallate?

The InChI Key for Ethyl Gallate is VFPFQHQNJCMNBZ-UHFFFAOYSA-N.

What is the purity of Ethyl Gallate?

The purity of Ethyl Gallate is 98%.

What is the appearance of Ethyl Gallate?

The appearance of Ethyl Gallate is a white powder.

What is the percentage of actives in Ethyl Gallate?

The percentage of actives in Ethyl Gallate is 95%.

What is the physical state of Ethyl Gallate?

The physical state of Ethyl Gallate is a solid.

What is a typical application of Ethyl Gallate?

A typical application of Ethyl Gallate is as an antioxidant.

Synthetic Use

Upstream Synthesis Route 1

• 64-17-5
• 149-91-7

• 831-61-8

Reference: [1] Patent: CN105294433, 2016, A, . Location in patent: Paragraph 0026

Upstream Synthesis Route 2

• 100079-21-8

• 831-61-8

Reference: [1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 17, p. 7975 - 7982

Upstream Synthesis Route 3

• 73607-60-0

• 831-61-8

Reference: [1] Tetrahedron, 1997, vol. 53, # 6, p. 2163 - 2176

Upstream Synthesis Route 4

• 64-17-5
• 149-91-7

• 831-61-8

Reference: [1]Current Patent Assignee: HUNAN NORMAL UNIVERSITY - CN105294433, 2016, A
Location in patent: Paragraph 0026

Downstream Synthesis Route 1

• 831-61-8

• 5782-85-4

Reference: [1]Wang, Liang; Guo, Da-Gang; Wang, Yan-Yan; Zheng, Chang-Zheng
[RSC Advances, 2014, vol. 4, # 102, p. 58895 - 58901]

Downstream Synthesis Route 2

• 831-61-8

• 476-66-4

Reference: [1]Current Patent Assignee: GUIYANG BEILONG BIOTECHNOLOGY - CN110066284, 2019, A
Location in patent: Paragraph 0053-0054
[2]Ernst; Zwenger
[Justus Liebigs Annalen der Chemie, 1871, vol. 159, p. 33]
Schiff
[Justus Liebigs Annalen der Chemie, 1872, vol. 163, p. 218][Chemische Berichte, 1879, vol. 12, p. 1533]
[3]Herzig; Pollak; v. Bronneck
[Monatshefte fur Chemie, 1908, vol. 29, p. 278]
[4]Trivedi, K. K.; Kochak, Geeta; Misra, K.
[Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1983, vol. 22, # 9, p. 925 - 926]
[5]Current Patent Assignee: GUIYANG BEILONG BIOTECHNOLOGY - CN108395440, 2018, A

* For details of the synthesis route, please refer to the original source to ensure accuracy.