W379905
1,2-ジメトキシベンゼン
≥99%, FG
別名:
ピロカテコールジメチルエーテル, ベラトロール
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この商品について
化学式:
C6H4(OCH3)2
CAS番号:
分子量:
138.16
FEMA Number:
3799
Council of Europe no.:
10320
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
4.062
EC Number:
202-045-3
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
1364621
Organoleptic:
anise; clove; spicy; vanilla
Grade:
FG
Fragrance grade
Halal
Fragrance grade
Halal
Biological source:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
meets purity specifications of JECFA
Food allergen:
no known allergens
製品名
1,2-ジメトキシベンゼン, ≥99%, FG
SMILES string
COc1ccccc1OC
InChI
1S/C8H10O2/c1-9-7-5-3-4-6-8(7)10-2/h3-6H,1-2H3
InChI key
ABDKAPXRBAPSQN-UHFFFAOYSA-N
biological source
synthetic
grade
FG
Fragrance grade
Halal
agency
follows IFRA guidelines
meets purity specifications of JECFA
reg. compliance
EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
assay
≥99%
refractive index
n20/D 1.533 (lit.)
bp
206-207 °C (lit.)
mp
15 °C (lit.)
density
1.084 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
fragrance allergen
no known allergens
organoleptic
anise; clove; spicy; vanilla
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Journal of insect physiology, 49(12), 1125-1133 (2003-11-20)
Mature gregarious male desert locusts, Schistocerca gregaria, emit the courtship inhibition pheromone phenylacetonitrile. Wings and legs, in particular the fore wings, have been identified as the main releasing sites. Abdomen and head emit only trace amounts of this pheromone. In
Anke Siebert et al.
Archives of microbiology, 183(6), 378-384 (2005-06-22)
The anaerobic veratrol O-demethylase mediates the transfer of the methyl group of the phenyl methyl ether veratrol to tetrahydrofolate. The primary methyl group acceptor is the cobalt of a corrinoid protein, which has to be in the +1 oxidation state
Vincent J Chebny et al.
Organic letters, 11(11), 2253-2256 (2009-05-29)
Definitive X-ray crystallographic evidence is obtained for a single hole (or a polaron) to be uniformly distributed on the three equivalent 1,2-dimethoxybenzenoid (or veratrole) rings in the hexamethoxytriptycene cation radical. This conclusion is further supported by electrochemical analysis and by
M K Tse et al.
Organic letters, 3(18), 2831-2833 (2001-09-01)
[reaction: see text]. A protocol for performing Rh catalyzed aromatic borylations in cyclohexane has been devised. Borylation at the 5-position of several 1,3-substituted aromatic species ranging from electron-rich (1,3-(NMe(2))(2)C(6)H(4)) to electron-deficient (1,3-(CF(3))(2)C(6)H(4)) yields the corresponding aryl boronate esters. Veratrole was
The absorption of hydrophobic chemicals across perfused rainbow trout gills: methodological aspects.
P Pärt et al.
Ecotoxicology and environmental safety, 24(3), 275-286 (1992-12-01)
The absorption rates of 4-bromophenol, 2,4-dibromophenol, 3,4,5-trichloroguaiacol, and tetrachloroveratrol across fish gill epithelium have been measured in a perfused gill preparation from rainbow trout (Oncorhynchus mykiss). In additional experiments the absorption rate of tetrachloroveratrol was measured in free swimming fish.
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