47168
3,5-Di-tert-butyl-4-hydroxytoluene
analytical standard
Synonym(s):
3,5-Di-tert-butyl-4-hydroxytoluene, E321
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About This Item
CAS Number:
UNSPSC Code:
12164500
PubChem Substance ID:
EC Number:
204-881-4
MDL number:
NACRES:
NA.24
grade
analytical standard
CofA
current certificate can be downloaded
packaging
pkg of 500 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
cleaning products
cosmetics
food and beverages
personal care
format
neat
storage temp.
room temp
SMILES string
Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C
InChI
1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3
InChI key
NLZUEZXRPGMBCV-UHFFFAOYSA-N
Gene Information
human ... CAPN1(823)
rat ... Capn1(29153), Nos1(24598)
General description
3,5-Di-tert-4-butylhydroxytoluene belongs to the class of phenolic antioxidants, added to food and other products such as oils, fats and butter oil to prevent rancidity caused by the oxidation of unsaturated fats.
Application
3,5-Di-tert-4-butylhydroxytoluene may be used as an analytical reference standard for the quantification of the analyte in Eucalyptus wood using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
signalword
Warning
hcodes
pcodes
Storage Class
11 - Combustible Solids
flash_point_f
260.6 °F - open cup
flash_point_c
127 °C - open cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Hazard Classifications
Aquatic Chronic 1
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Supercritical fluid extraction of phenolic compounds from Eucalyptus globulus Labill bark
Santos.O.AS, et al.
Journal of Supercritical Fluids, 71, 71-79 (2012)
Ultra-high performance liquid chromatography coupled to mass spectrometry applied to the identification of valuable phenolic compounds from Eucalyptus wood
Santos.O.AS, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 938, 65-74 (2013)
Santo Scalia et al.
Molecules (Basel, Switzerland), 18(1), 574-587 (2013-01-08)
The catechin (-)-epigallocatechin-3-gallate (EGCG) exhibits high antioxidant activity and it has been reported to provide protection of the skin against damage induced by solar UV radiation. However, EGCG is highly unstable under sunlight. The present study aimed to compare the