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Merck
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Documentos

176893

Sigma-Aldrich

2-Methoxyhydroquinone

98%

Sinónimos:

2,5-Dihydroxyanisol

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About This Item

Fórmula lineal:
(CH3O)C6H3(OH)2
Número de CAS:
824-46-4
Peso molecular:
140.14
Beilstein/REAXYS Number:
2045285
EC Number:
212-530-1
MDL number:
MFCD00013971
UNSPSC Code:
12162002
PubChem Substance ID:
24850606
NACRES:
NA.23

Quality Level

100

assay

98%

form

solid

mp

88-91 °C (lit.)

SMILES string

COc1cc(O)ccc1O

InChI

1S/C7H8O3/c1-10-7-4-5(8)2-3-6(7)9/h2-4,8-9H,1H3

InChI key

LAQYHRQFABOIFD-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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David Sillam-Dussès et al.
PloS one, 7(10), e46431-e46431 (2012-10-17)
Labial glands are present in all castes and developmental stages of all termite species. In workers, their secretion contains a food-marking pheromone and digestive enzymes, while soldier secretion plays a defensive role. However, these functions were studied only in a
Shou Ito et al.
Biotechnology for biofuels, 13, 18-18 (2020-02-06)
Vanillin is the main byproduct of alkaline-pretreated lignocellulosic biomass during the process of fermentable-sugar production and a potent inhibitor of ethanol production by yeast. Yeast cells are usually exposed to vanillin during the industrial production of bioethanol from lignocellulosic biomass.
Koorosh Ashrafi et al.
International journal of pharmaceutics, 524(1-2), 226-237 (2017-04-05)
Drug release from chemoembolization microspheres stimulated by the presence of a chemically reducing environment may provide benefits for targeting drug resistant and metastatic hypoxic tumours. A water-soluble disulfide-based bifunctional cross-linker bis(acryloyl)-(l)-cystine (BALC) was synthesised, characterised and incorporated into a modified
Maher A Qaddoura et al.
International journal of molecular sciences, 10(11), 4772-4788 (2010-01-21)
Several divinylic mesogenic monomers were synthesized based on coupling the monomer 4-(4-pentenyloxy)benzoic acid with chlorohydroquinone, 2,5-dihydroxy- acetophenone, methylhydroquinone or 2-methoxyhydroquinone. This resulted in novel mesogens of phenylene esters with different lateral substituent groups. The effect of the lateral substituent group
Denilson F Oliveira et al.
Experimental parasitology, 199, 17-23 (2019-02-23)
Exposing second-stage juveniles (J2) of Meloidogyne incognita in vitro to a phenolic compound sometimes fails to cause J2 mortality, but in tests in vivo the same compound may reduce the infectivity and population of the nematode. This work aimed to

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