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

  • ≥98%
Item Number
O137952
Grouped product items
SKUSizeAvailabilityPrice Qty
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

SynonymsOctyl gallate|1034-01-1|Octyl 3,4,5-trihydroxybenzoate|n-Octyl gallate|Progallin O|Stabilizer GA 8|n-Octylgallate|Gallic acid, octyl ester|BENZOIC ACID, 3,4,5-TRIHYDROXY-, OCTYL ESTER|Gallic acid octyl ester|Gallic acid n-octyl ester|Oktylester kyseliny g
Specifications & Purity≥98%
Shipped InNormal
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

SQLE Tchem Squalene monooxygenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ESR1 Tclin Estrogen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR3C1 Tclin Glucocorticoid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AR Tclin Androgen receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AKR1B1 Tclin Aldose reductase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT2A1 Tbio UDP-glucuronosyltransferase 2A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

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

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488183469
Pubchem Sid Urlhttps://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)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

7 results found

Lot NumberCertificate TypeDateItem
K2117081Certificate of AnalysisSep 14, 2023 O137952
K2117124Certificate of AnalysisSep 14, 2023 O137952
K2117126Certificate of AnalysisSep 14, 2023 O137952
K2117132Certificate of AnalysisSep 14, 2023 O137952
C2115118Certificate of AnalysisDec 15, 2022 O137952
C23241023Certificate of AnalysisSep 09, 2021 O137952
D2324190Certificate of AnalysisSep 09, 2021 O137952

Chemical and Physical Properties

Solubilitysouble 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

Related Documents

References

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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]
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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]
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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]
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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]
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