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关于此项目
线性分子式:
CH3OC6H4CHO
化学文摘社编号:
分子量:
136.15
FEMA Number:
2670
Council of Europe no.:
103
UNSPSC Code:
12164502
PubChem Substance ID:
NACRES:
NA.21
EC Number:
204-602-6
Flavis number:
5.015
MDL number:
Beilstein/REAXYS Number:
471382
Organoleptic:
anise; cherry; creamy; floral; balsamic; sweet; vanilla
Grade:
FG, Fragrance grade, Halal, Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines, meets purity specifications of JECFA
Food allergen:
no known allergens
biological source
synthetic
grade
FG, Fragrance grade, Halal, Kosher
agency
follows IFRA guidelines, meets purity specifications of JECFA
reg. compliance
EU Regulation 1223/2009, EU Regulation 1334/2008 & 872/2012, FCC, FDA 21 CFR 172.515
vapor density
4.7 (vs air)
assay
≥97.5%
form
liquid
composition
contains IFRA restricted p-Anisaldehyde
refractive index
n20/D 1.573 (lit.)
bp
248 °C (lit.)
mp
−1 °C (lit.)
density
1.119 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; cherry; creamy; floral; balsamic; sweet; vanilla
SMILES string
[H]C(=O)c1ccc(OC)cc1
InChI
1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3
InChI key
ZRSNZINYAWTAHE-UHFFFAOYSA-N
Gene Information
human ... CYP1A2(1544)
Application
- Aryl-alcohol oxidase involved in lignin degradation: a mechanistic study based on steady and pre-steady state kinetics and primary and solvent isotope effects with two alcohol substrates.: The study focuses on the mechanistic understanding of aryl-alcohol oxidase in lignin degradation, utilizing p-Anisaldehyde as a model substrate to investigate enzyme kinetics and isotope effects. (Ferreira et al., 2009).
Biochem/physiol Actions
1.0% 时的气味
5-10ppm 时的味道
Other Notes
天然存在:香草、茴香、八角茴香、曼越橘、黑加仑、肉桂、罗勒。
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 3 - Repr. 2
存储类别
10 - Combustible liquids
flash_point_f
240.8 °F - closed cup
flash_point_c
116 °C - closed cup
Tae Joung Ha et al.
Journal of agricultural and food chemistry, 53(18), 7024-7028 (2005-09-01)
Anisaldehyde (p-methoxybenzaldehyde) was previously reported to inhibit the tyrosinase-catalyzed oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) noncompetitively as long as the enzyme activity was monitored by measuring dopachrome formation. However, anisaldehyde did not inhibit this oxidation if a longer reaction time was observed
Haruki Mizoguchi et al.
Organic & biomolecular chemistry, 13(21), 5955-5963 (2015-05-01)
Copper-catalyzed 6-endo cyclization of N-propargylic β-enaminocarbonyls was developed for the synthesis of oxidation-labile 1,6-dihydropyridines. This synthetic method allows flexible and regio-defined assembly of various substituents at the N1, C2, C3, C4, and C6 positions of 1,6-dihydropyridines under mild conditions.
Víctor Gómez-Toribio et al.
Applied and environmental microbiology, 75(12), 3954-3962 (2009-04-21)
The induction of hydroxyl radical (OH) production via quinone redox cycling in white-rot fungi was investigated to improve pollutant degradation. In particular, we examined the influence of 4-methoxybenzaldehyde (anisaldehyde), Mn(2+), and oxalate on Pleurotus eryngii OH generation. Our standard quinone
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| W267007-5KG-K | 04061837835056 |
| W267007-SAMPLE-K | 04061837835063 |
| W267007-1KG-K | 04061837835032 |
| W267007-25KG-K | 04061837835049 |
