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367079

Sigma-Aldrich

Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate

99%

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About This Item

Linear Formula:
[(CH3)3C]2C6H2(OH)CH2CH2CO2(CH2)17CH3
CAS Number:
2082-79-3
Molecular Weight:
530.86
EC Number:
218-216-0
MDL number:
MFCD00017498
UNSPSC Code:
12162002
PubChem Substance ID:
24862391
NACRES:
NA.23

Assay

99%

form

powder

mp

50-52 °C (lit.)

SMILES string

CCCCCCCCCCCCCCCCCCOC(=O)CCc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C

InChI

1S/C35H62O3/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-26-38-32(36)25-24-29-27-30(34(2,3)4)33(37)31(28-29)35(5,6)7/h27-28,37H,8-26H2,1-7H3

InChI key

SSDSCDGVMJFTEQ-UHFFFAOYSA-N

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General description

Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate is a propionate based phenolic antioxidant that can be used as a polymeric stabilizer by butylphenol functionalities.

Storage Class Code

11 - Combustible Solids

WGK

nwg

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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E Niki et al.
The Journal of biological chemistry, 260(4), 2191-2196 (1985-02-25)
Inhibition of the oxidation of methyl linoleate and soybean phosphatidylcholine in homogeneous solution and in aqueous dispersion by four chain-breaking antioxidants, vitamin E (alpha-tocopherol), 2,2,5,7,8-pentamethyl-6-chromanol, 2,6-di-tert-butyl-4-methylphenol, and stearyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, was studied to examine the effect of the phytyl side chain
Johanna Saunier et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 75(3), 443-450 (2010-05-04)
Irganox 1076(R) (octadecyl-3,5-di-tert-butyl-4-hydroxyhydrocinnamate) is a common phenolic antioxidant used in many polymer-based medical devices. As with many organic compounds, several polymorphs exist. However, in literature, only two forms of Irganox 1076(R) have been mentioned. In this study, we were able
P Molander et al.
Journal of chromatography. A, 864(1), 103-109 (2000-01-12)
Sub-ambient column temperatures, promoting strong interactions between the analyte and the stationary phase material, were utilized to focus large volumes of the polyolefin antioxidant Irganox 1076 [benzenepropanoic acid, 3.5-bis(1,1-dimethylethyl)-4-hydroxy-, octadecyl ester] on the column inlet, using pure acetonitrile as sample
The induction of rat hepatic microsomal xenobiotic metabolism by n-octadecyl beta-(3',5'-di-tert-butyl-4'-hydroxyphenyl)-propionate.
B G Lake et al.
Food and cosmetics toxicology, 18(1), 47-54 (1980-02-01)
I E Helmroth et al.
Food additives and contaminants, 19(2), 176-183 (2002-02-01)
The effect of solvent absorption on additive migration was studied by relating the diffusion coefficient (D) of Irganox 1076 to the maximum solvent absorption of different solvents in low-density polyethylene (LDPE) film. Solvents tested were ethanol, isopropanol, isooctane, ethylacetate, cyclohexane
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