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Safety Information

D131350

Sigma-Aldrich

1,4-Dimethoxybenzene

ReagentPlus®, 99%

Synonym(s):

p-Methoxyanisole, Dimethylhydroquinone, Hydroquinone dimethyl ether, NSC 7483

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About This Item

Linear Formula:
C6H4(OCH3)2
CAS Number:
150-78-7
Molecular Weight:
138.16
Beilstein:
774605
EC Number:
205-771-9
MDL number:
MFCD00008401
UNSPSC Code:
12352100
PubChem Substance ID:
24893410
NACRES:
NA.22

vapor density

4.8 (vs air)

Quality Level

100

vapor pressure

<1 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

99%

form

crystals

autoignition temp.

1463 °F

bp

213 °C (lit.)

mp

54-56 °C (lit.)

density

1.053 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(OC)cc1

InChI

1S/C8H10O2/c1-9-7-3-5-8(10-2)6-4-7/h3-6H,1-2H3

InChI key

OHBQPCCCRFSCAX-UHFFFAOYSA-N

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

257.0 °F - closed cup

Flash Point(C)

125 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

D131350-BULK:
D131350-10KG:
D131350-1KG:
D131350-VAR:
D131350-5G:
D131350-100G:
D131350-500G:

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2793
STBK7569
STBK8136
STBK0394
STBK0097

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H J Altmann et al.
Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement, 8, 114-116 (1985-01-01)
Butylated hydroxyanisole (BHA) is widely used as an antioxidant in foodstuffs, in materials which come into contact with food and also in cosmetic products. The safety of BHA was questioned, however, when it was reported that in a recent Japanese
Tiantian Li et al.
The journal of physical chemistry. A, 115(19), 4988-4994 (2011-04-27)
The effect of substituents on the oxidation potential for the one-electron reaction of 1,4-dimethoxybenzene was understood with a theoretical calculation based on density functional theory (DFT) at the level of B3LYP/6-311+G(d). It is found that the oxidation potential for the
D W Kim et al.
Organic letters, 3(3), 445-447 (2001-06-29)
[figure: see text] Fused 1,4-dimethoxybenzenes could be oxidized to benzoquinones by either direct oxidation or demethylation-oxidation. The oxidative demethylation of 5,8-dimethoxy-2-methylquinoline using 1.1 equiv of NBS in aqueous THF and a catalytic amount of H2SO4 at 20 degrees C for
M Masuda et al.
Bioscience, biotechnology, and biochemistry, 60(5), 806-810 (1996-05-01)
Bovine serum albumin (BSA) added to the reaction medium for the oxidative demethylation of 4-methoxyanisole and its "di-CD3" isotopomer ([d6]methoxyanisole), when catalyzed by liver microsomes from untreated rats, decreased the Km values and increased the V(max)/Km (= V/K) values. The
D K Joshi et al.
European journal of biochemistry, 237(1), 45-57 (1996-04-01)
The stabilities of the cation radicals of veratryl alcohol, 3,4-dimethoxytoluene and 1,4-dimethoxybenzene were compared by monitoring the formation of dimeric products during the oxidation of these substrates by lignin peroxidase (LiP). LiP oxidized veratryl alcohol to generate veratraldehyde as the
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