Skip to Content
Merck
CN

T76503

Trimethylhydroquinone

97%

Synonym(s):

1,4-Dihydroxy-2,3,5-trimethylbenzene, 3,6-Dihydroxypseudocumene

Sign In to View Organizational & Contract Pricing

Select a Size

About This Item

Linear Formula:
(CH3)3C6H-1,4-(OH)2
CAS Number:
700-13-0
Molecular Weight:
152.19
Beilstein:
1909183
EC Number:
211-838-3
MDL number:
MFCD00002346
UNSPSC Code:
12352100
PubChem Substance ID:
24900467
NACRES:
NA.22

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Assay

97%

mp

169-172 °C (lit.)

SMILES string

Cc1cc(O)c(C)c(C)c1O

InChI

1S/C9H12O2/c1-5-4-8(10)6(2)7(3)9(5)11/h4,10-11H,1-3H3

InChI key

AUFZRCJENRSRLY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Trimethylhydroquinone is a key precursor for the synthesis of tocopherols (vitamin E) and (±)-madindolines.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

375.8 °F - closed cup

Flash Point(C)

191 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF5622V
WXBF3757V
WXBF3576V
WXBD6991V
WXBD6611V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

P R Rich
Biochimica et biophysica acta, 722(2), 271-280 (1983-02-17)
(1) A kinetic analysis of electron donation into and through the cytochrome b-c1 complex isolated from bovine heart mitochondria has been undertaken, using trimethoquinol as the donor. (2) Rate constants of two routes of redox equilibration with quinols have been
Enantioselective Palladium-Catalyzed Total Synthesis of Vitamin E by Employing a Domino Wacker-Heck Reaction.
Tietze, Lutz F et al.
Chemistry?A European Journal , 12(34), 8770-8776 (2006)
Vitaly A Roginsky et al.
Aging, 1(5), 481-489 (2010-03-03)
The chain-breaking antioxidant activities of reduced form of novel type of geroprotectors, mitochondria-targeted quinones (QH(2)) have quantitatively been measured for the first time. To this end, the chain peroxidation of methyl linoleate (ML) in Triton micelles was used as a
Synthesis of (?)-madindolines and chemical models. Studies of chemical reactivity.
McComas, Casey C et al.
Organic Letters, 4(14), 2337-2340 (2002)
U Burner et al.
Redox report : communications in free radical research, 5(4), 185-190 (2000-09-20)
Myeloperoxidase is very susceptible to reducing radicals because the reduction potential of the ferric/ferrous redox couple is much higher compared with other peroxidases. Semiquinone radicals are known to reduce heme proteins. Therefore, the kinetics and spectra of the reactions of
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service