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Merck
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文件

W267007

Sigma-Aldrich

对茴香醛

≥97.5%, FCC, FG

别名:

对甲氧基苯甲醛, 茴香醛

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About This Item

线性分子式:
CH3OC6H4CHO
CAS号:
123-11-5
分子量:
136.15
FEMA號碼:
2670
Beilstein:
471382
EC號碼:
204-602-6
歐洲委員會號碼:
103
MDL號碼:
MFCD00003385
分類程式碼代碼:
12164502
PubChem物質ID:
24901235
Flavis號碼:
5.015
NACRES:
NA.21

生物源

synthetic

等級

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FCC
FDA 21 CFR 172.515

蒸汽密度

4.7 (vs air)

化驗

≥97.5%

形狀

liquid

成份

contains IFRA restricted p-Anisaldehyde

折射率

n20/D 1.573 (lit.)

bp

248 °C (lit.)

mp

−1 °C (lit.)

密度

1.119 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

no known allergens

感官的

anise; cherry; creamy; floral; balsamic; sweet; vanilla

SMILES 字串

[H]C(=O)c1ccc(OC)cc1

InChI

1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

InChI 密鑰

ZRSNZINYAWTAHE-UHFFFAOYSA-N

基因資訊

human ... CYP1A2(1544)

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相关类别

應用


  • 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).

生化／生理作用

1.0% 时的气味
5-10ppm 时的味道

其他說明

天然存在：香草、茴香、八角茴香、曼越橘、黑加仑、肉桂、罗勒。

象形圖

Health hazard
GHS08

訊號詞

Warning

危險聲明

H361fd,H412

危險分類

Aquatic Chronic 3 - Repr. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 1

閃點（°F）

240.8 °F - closed cup

閃點（°C）

116 °C - closed cup

分析证书(COA)

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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
Guozhu Zhang et al.
Journal of the American Chemical Society, 130(38), 12598-12599 (2008-08-30)
A novel approach to generate Au-containing all-carbon 1,3-dipoles is developed via an unprecedented migration-fragmentation of ketals/acetals. These in situ generated dipoles undergo rapid [3+2] cycloaddition under mild conditions with various enones/enals, electron-rich aromatic aldehydes, and N-benzylindole, leading to flexible formation
N Juillet et al.
Plant biology (Stuttgart, Germany), 13(4), 570-575 (2011-06-15)
It has often been proposed that nectarless deceptive orchid species exploit naïve pollinators in search of food before they learn to avoid their flowers, and that intraspecific floral trait polymorphism, often noted in this plant group, could prolong the time
Israt Jahan et al.
Acta pharmaceutica (Zagreb, Croatia), 60(2), 207-215 (2010-12-08)
In this study, five compounds, lupeol (1), epilupeol (2), β-sitosterol (3), stigmasterol (4) and p-methoxybenzaldehyde (5) were isolated from the petroleum ether and dichloromethane fractions of a methanolic extract of the stem bark of Delonix regia. Antimicrobial screening of the
Wenxin Gu et al.
Organic letters, 5(4), 415-418 (2003-02-14)
[reaction: see text] Two new 4-methoxybenzaldehyde backbone linker resins were developed for the solid-phase synthesis of peptides. The linkers are very stable during the cleavage of common protecting groups for amines (Fmoc, Boc) and carboxylic acids (Me, All, tBu) in
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