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Octyl gallate - ≥98.0%, high purity , CAS No.1034-01-1

2 Citations

≥98%

CAS#: 1034-01-1
Formula: C₁₅H₂₂O₅
Molecular Weight: 282.33
Beilstein Registry Number: 2132305
EC Number: 213-853-0
MDL number: MFCD00002197
PubChem CID: 61253
PubChem SID: 488183469

Item Number

O137952

Grouped product items
SKU	Size	Availability	Price
O137952-5g	5g	In stock	$9.90
O137952-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$35.90
O137952-100g	100g	In stock	$101.90
O137952-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$457.90

View related series

Carbonyl compound carboxylic acid

Basic Description

Synonyms	DTXCID2020713 \| octyl 3,4,5-trihydroxybenzoate;Octyl gallate \| 4-10-00-02005 (Beilstein Handbook Reference) \| Octyl gallate, European Pharmacopoeia (EP) Reference Standard \| Oktylester kyseliny gallove [Czech] \| n-Octylgallate \| OCTIL GALLATE [MART.] \| BE
Specifications & Purity	≥98%
Shipped In	Normal
Product Description	Octyl gallate was used in a study to investigate the self-assembly in two comb-shaped supramolecules systems consisting of octyl gallate, hydrogen bonded to the pyridine groups of polyisoprene-block-poly(vinylpyridine) diblock copolymers using synchrotron radiation.

Associated Targets(Human)

SQLE Tchem Squalene monooxygenase (0 Activities)

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ESR1 Tclin Estrogen receptor (0 Activities)

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NR3C1 Tclin Glucocorticoid receptor (0 Activities)

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UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (0 Activities)

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UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (0 Activities)

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UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (0 Activities)

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AKR1C4 Tchem Aldo-keto reductase family 1 member C4 (0 Activities)

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AKR1C2 Tchem Aldo-keto reductase family 1 member C2 (0 Activities)

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AKR1C3 Tchem Aldo-keto reductase family 1 member C3 (0 Activities)

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AKR1B10 Tchem Aldo-keto reductase family 1 member B10 (0 Activities)

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AKR1C1 Tchem Aldo-keto reductase family 1 member C1 (0 Activities)

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AR Tclin Androgen receptor (0 Activities)

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AKR1B1 Tclin Aldose reductase (0 Activities)

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AKR1A1 Tchem Alcohol dehydrogenase [NADP(+)] (0 Activities)

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UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (0 Activities)

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UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (0 Activities)

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UGT2A1 Tbio UDP-glucuronosyltransferase 2A1 (0 Activities)

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NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (0 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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AKR1B1 Tclin Aldose reductase (1404 Activities)

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AKR1A1 Tchem Aldehyde reductase (91 Activities)

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NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)

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CCRF-CEM (65223 Activities)

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MCF7 (126967 Activities)

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AKR1C3 Tchem Aldo-keto-reductase family 1 member C3 (1414 Activities)

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AKR1C4 Tchem Aldo-keto reductase family 1 member C4 (224 Activities)

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AKR1C2 Tchem Aldo-keto reductase family 1 member C2 (639 Activities)

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AKR1C1 Tchem Aldo-keto reductase family 1 member C1 (475 Activities)

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AKR1B10 Tchem Aldo-keto reductase family 1 member B10 (300 Activities)

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UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)

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UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)

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UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (106 Activities)

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UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)

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UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)

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UGT2A1 UDP-glucuronosyltransferase 2A1 (59 Activities)

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Associated Targets(non-human)

ERG1 Squalene monooxygenase (20 Activities)

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Nannizzia gypsea (2039 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Ralstonia solanacearum (520 Activities)

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Proteus vulgaris (5823 Activities)

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Micrococcus luteus (7463 Activities)

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Staphylococcus aureus (210822 Activities)

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Klebsiella aerogenes (4963 Activities)

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Escherichia coli (133304 Activities)

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Streptococcus mutans (2687 Activities)

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Aspergillus flavus (8875 Activities)

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Aspergillus niger (16508 Activities)

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Bacillus subtilis (32866 Activities)

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Saccharomyces cerevisiae (19171 Activities)

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Corynebacterium ammoniagenes (75 Activities)

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Cutibacterium acnes (887 Activities)

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Zygosaccharomyces bailii (36 Activities)

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Aspergillus fumigatus (16427 Activities)

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Cryptococcus neoformans (21258 Activities)

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Candida albicans (78123 Activities)

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Candida tropicalis (8381 Activities)

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Trichophyton rubrum (3646 Activities)

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Human respirovirus 3 (1674 Activities)

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Vaccinia virus (4609 Activities)

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Human immunodeficiency virus 1 (70413 Activities)

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Reovirus sp. (323 Activities)

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Sindbis virus (1599 Activities)

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Vesicular stomatitis virus (4460 Activities)

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Influenza A virus (11224 Activities)

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Punta Toro virus (1491 Activities)

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Human immunodeficiency virus 2 (5592 Activities)

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Coxsackievirus B4 (2249 Activities)

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Respiratory syncytial virus (3434 Activities)

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Salmonella enterica (1497 Activities)

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Epidermophyton floccosum (561 Activities)

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L1210 (27553 Activities)

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L929 (3802 Activities)

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B16-F10 (4610 Activities)

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Aspergillus parasiticus (296 Activities)

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Coptotermes formosanus (677 Activities)

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Felid alphaherpesvirus 1 (460 Activities)

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Feline coronavirus (624 Activities)

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Trichophyton mentagrophytes (4846 Activities)

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Influenza A virus H3N2 (588 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488183469
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488183469
IUPAC Name	octyl 3,4,5-trihydroxybenzoate
INCHI	InChI=1S/C15H22O5/c1-2-3-4-5-6-7-8-20-15(19)11-9-12(16)14(18)13(17)10-11/h9-10,16-18H,2-8H2,1H3
InChi Key	NRPKURNSADTHLJ-UHFFFAOYSA-N
Canonical SMILES	CCCCCCCCOC(=O)C1=CC(=C(C(=C1)O)O)O
Isomeric SMILES	CCCCCCCCOC(=O)C1=CC(=C(C(=C1)O)O)O
WGK Germany	1
RTECS	LW8225000
PubChem CID	61253
Molecular Weight	282.33
Beilstein	2132305

Certificates

Certificate of Analysis(COA)

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Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number	Certificate Type	Date	Item
L2405591	Certificate of Analysis	Apr 02, 2024	O137952
K2117081	Certificate of Analysis	Sep 14, 2023	O137952
K2117124	Certificate of Analysis	Sep 14, 2023	O137952
K2117126	Certificate of Analysis	Sep 14, 2023	O137952
K2117132	Certificate of Analysis	Sep 14, 2023	O137952
K2427193	Certificate of Analysis	Sep 14, 2023	O137952
L2410090	Certificate of Analysis	Sep 14, 2023	O137952
C2115118	Certificate of Analysis	Dec 15, 2022	O137952
C23241023	Certificate of Analysis	Sep 09, 2021	O137952
D2324190	Certificate of Analysis	Sep 09, 2021	O137952

Chemical and Physical Properties

Solubility	souble in Methanol
Melt Point(°C)	100 °C

Safety and Hazards(GHS)

Pictogram(s)	GHS07
Signal	Warning
Hazard Statements	H302:Harmful if swallowed H317:May cause an allergic skin reaction
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P272:Contaminated work clothing should not be allowed out of the workplace. P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention. P362+P364:Take off contaminated clothing and wash it before reuse. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help.
WGK Germany	1
RTECS	LW8225000

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yuling Li, Xiaotong Wu, Zixuan Wu, Mingmin Zhong, Xiaoping Su, Youai Ye, Yan Liu, Lei Tan, Yong Liang. (2022) Colorimetric sensor array based on CoOOH nanoflakes for rapid discrimination of antioxidants in food. Analytical Methods, 14 (28): (2754-2760). [PMID:35781305]
2. Man-Tong Zhao, Zhong-Yuan Liu, Guan-Hua Zhao, De-Yang Li, Guang-Hua Xia, Fa-Wen Yin, Da-Yong Zhou. (2022) Investigation of the antioxidation capacity of gallic acid and its alkyl esters with different chain lengths for dried oyster during ambient storage. INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY, 57 (4): (2435-2446). [PMID:]

References

1. Isao Kubo,Ken-Ichi Fujita,Ken-Ichi Nihei. (2002-10-31) Anti-Salmonella activity of alkyl gallates.. Journal of agricultural and food chemistry, 50 ((23)): (6692-6696). [PMID:12405763]
2. Matthew G Soars,Edward L Mattiuz,David A Jackson,Palaniappan Kulanthaivel,William J Ehlhardt,Steven A Wrighton. (2003-03-12) Biosynthesis of drug glucuronides for use as authentic standards.. Journal of pharmacological and toxicological methods, 47 ((3)): (161-168). [PMID:12628307]
3. Isao Kubo,Ken-ichi Fujita,Ken-ichi Nihei,Atsuko Nihei. (2004-03-05) Antibacterial activity of akyl gallates against Bacillus subtilis.. Journal of agricultural and food chemistry, 52 ((5)): (1072-1076). [PMID:14995100]
4. Gavin A E Wong,Neil H Shear. (2004-03-05) Melkersson-Rosenthal syndrome associated with allergic contact dermatitis from octyl and dodecyl gallates.. Contact dermatitis, 49 ((5)): (266-267). [PMID:14996058]
5. Paul D Stapleton,Saroj Shah,James C Anderson,Yukihiko Hara,Jeremy M T Hamilton-Miller,Peter W Taylor. (2004-05-04) Modulation of beta-lactam resistance in Staphylococcus aureus by catechins and gallates.. International journal of antimicrobial agents, 23 ((5)): (462-467). [PMID:15120724]
6. Liisa Törmäkangas,Pia Vuorela,Elise Saario,Maija Leinonen,Pekka Saikku,Heikki Vuorela. (2005-09-06) In vivo treatment of acute Chlamydia pneumoniae infection with the flavonoids quercetin and luteolin and an alkyl gallate, octyl gallate, in a mouse model.. Biochemical pharmacology, 70 ((8)): (1222-1230). [PMID:16139801]
7. K Kreander,P Vuorela,P Tammela. (2006-05-10) A rapid screening method for detecting active compounds against erythromycin-resistant bacterial strains of Finnish origin.. Folia microbiologica, 50 ((6)): (487-493). [PMID:16681145]
8. Misao Uozaki,Hisashi Yamasaki,Yukiko Katsuyama,Masanori Higuchi,Tomihiko Higuti,A Hajime Koyama. (2006-09-05) Antiviral effect of octyl gallate against DNA and RNA viruses.. Antiviral research, 73 ((2)): (85-91). [PMID:16950523]
9. Hisashi Yamasaki,Misao Uozaki,Yukiko Katsuyama,Hirotoshi Utsunomiya,Tsutomu Arakawa,Masanori Higuchi,Tomihiko Higuti,A Hajime Koyama. (2007-03-06) Antiviral effect of octyl gallate against influenza and other RNA viruses.. International journal of molecular medicine, 19 ((4)): (685-688). [PMID:17334645]
10. M L García-Melgares,J de la Cuadra,B Martín,C Laguna,L Martínez,V Alegre. (2007-11-24) [Sensitization to gallates: review of 46 cases].. Actas dermo-sifiliograficas, 98 ((10)): (688-693). [PMID:18035026]
11. E Sierra-Campos,M A Valdez-Solana,D Matuz-Mares,I Velázquez,J P Pardo. (2009-02-10) Induction of morphological changes in Ustilago maydis cells by octyl gallate.. Microbiology (Reading, England), 155 ((Pt 2)): (604-611). [PMID:19202109]
12. Javier Rúa,Laura Fernández-Álvarez,Cristina de Castro,Pilar Del Valle,Dolores de Arriaga,María Rosario García-Armesto. (2010-11-03) Antibacterial activity against foodborne Staphylococcus aureus and antioxidant capacity of various pure phenolic compounds.. Foodborne pathogens and disease, 8 ((1)): (149-157). [PMID:21034269]
13. Clarissa A S de Cordova,Claudriana Locatelli,Laura S Assunção,Bruno Mattei,Alessandra Mascarello,Evelyn Winter,Ricardo J Nunes,Rosendo A Yunes,Tânia B Creczynski-Pasa. (2011-08-23) Octyl and dodecyl gallates induce oxidative stress and apoptosis in a melanoma cell line.. Toxicology in vitro : an international journal published in association with BIBRA, 25 ((8)): (2025-2034). [PMID:21856409]
14. Jun Liang,Richard D Ludescher. (2011-11-09) Antioxidants modulate molecular mobility, oxygen permeability, and microstructure in zein films.. Journal of agricultural and food chemistry, 59 ((24)): (13173-13180). [PMID:22060618]
15. Nagao Totani,Sayuri Tateishi,Tatsuya Takimoto,Risa Shinohara,Hideaki Sasaki. (2012-06-13) Ferulic acid esters and weight-loss promoting effects in rats.. Journal of oleo science, 61 ((6)): (331-336). [PMID:22687778]
16. Gabrielle Jacklin Eler,Israel Souza Santos,Amarilis Giaretta de Moraes,Márcio Shigueaki Mito,Jurandir Fernando Comar,Rosane Marina Peralta,Adelar Bracht. (2013-09-10) Kinetics of the transformation of n-propyl gallate and structural analogs in the perfused rat liver.. Toxicology and applied pharmacology, 273 ((1)): (35-46). [PMID:24012771]
17. I Kubo,P Xiao,K Fujita. (2001-02-24) Antifungal activity of octyl gallate: structural criteria and mode of action.. Bioorganic & medicinal chemistry letters, 11 ((3)): (347-350). [PMID:11212107]
18. Nurit Bar Nun,Dina Plakhine,Daniel M Joel,Alfred M Mayer. (2003-08-30) Changes in the activity of the alternative oxidase in Orobanche seeds during conditioning and their possible physiological function.. Phytochemistry, 64 ((1)): (235-241). [PMID:12946422]
19. Eve-Marie Josse,Jean-Pierre Alcaraz,Anne-Marie Labouré,Marcel Kuntz. (2003-09-03) In vitro characterization of a plastid terminal oxidase (PTOX).. European journal of biochemistry, 270 ((18)): (3787-3794). [PMID:12950262]
20. Anna Radomska. (2003-10-15) Antioxidant properties of captopril in vitro.. Acta poloniae pharmaceutica, 60 ((3)): (191-195). [PMID:14556487]
21. Tae Joung Ha,Ken-ichi Nihei,Isao Kubo. (2004-05-13) Lipoxygenase inhibitory activity of octyl gallate.. Journal of agricultural and food chemistry, 52 ((10)): (3177-3181). [PMID:15137872]
22. Fu-Lan Hsu,Hui-Ting Chang,Shang-Tzen Chang. (2006-06-06) Evaluation of antifungal properties of octyl gallate and its synergy with cinnamaldehyde.. Bioresource technology, 98 ((4)): (734-738). [PMID:16750625]
23. Tsutomu Arakawa,Yoshiko Kita,A Hajime Koyama. (2008-02-05) Solubility enhancement of gluten and organic compounds by arginine.. International journal of pharmaceutics, 355 ((1-2)): (220-223). [PMID:18242019]
24. Hirofumi Shibata,Tatsuro Nakano,M Anowar Khasru Parvez,Yoshihiro Furukawa,Akio Tomoishi,Shingo Niimi,Naokatu Arakaki,Tomihiko Higuti. (2009-02-19) Triple combinations of lower and longer alkyl gallates and oxacillin improve antibiotic synergy against methicillin-resistant Staphylococcus aureus.. Antimicrobial agents and chemotherapy, 53 ((5)): (2218-2220). [PMID:19223633]
25. Jiangxin Wang,Milton Sommerfeld,Qiang Hu. (2009-05-02) Occurrence and environmental stress responses of two plastid terminal oxidases in Haematococcus pluvialis (Chlorophyceae).. Planta, 230 ((1)): (191-203). [PMID:19408010]
26. Xiaojun Li,Liang Shang,Yaohua Wu,Suzanne Abbas,Dong Li,Patrick Netter,Mohamed Ouzzine,Hui Wang,Jacques Magdalou. (2011-03-23) Identification of the human UDP-glucuronosyltransferase isoforms involved in the glucuronidation of the phytochemical ferulic acid.. Drug metabolism and pharmacokinetics, 26 ((4)): (341-350). [PMID:21422672]
27. Yuling Li, Xiaotong Wu, Zixuan Wu, Mingmin Zhong, Xiaoping Su, Youai Ye, Yan Liu, Lei Tan, Yong Liang. (2022) Colorimetric sensor array based on CoOOH nanoflakes for rapid discrimination of antioxidants in food. Analytical Methods, 14 (28): (2754-2760). [PMID:35781305]
28. Man-Tong Zhao, Zhong-Yuan Liu, Guan-Hua Zhao, De-Yang Li, Guang-Hua Xia, Fa-Wen Yin, Da-Yong Zhou. (2022) Investigation of the antioxidation capacity of gallic acid and its alkyl esters with different chain lengths for dried oyster during ambient storage. INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY, 57 (4): (2435-2446). [PMID:]

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Octyl gallate - ≥98.0%, high purity , CAS No.1034-01-1

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