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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编号:
2670
Beilstein:
471382
EC 号:
204-602-6
欧洲委员会编号:
103
MDL编号:
MFCD00003385
UNSPSC代码:
12164502
PubChem化学物质编号:
24901235
Flavis编号:
5.015
NACRES:
NA.21
性状检查:
anise; cherry; creamy; floral; balsamic; sweet; vanilla
等级:
FG
Fragrance grade
Halal
Kosher
生物来源:
synthetic
Agency:
follows IFRA guidelines
meets purity specifications of JECFA
食品过敏原:
no known allergens

生物来源

synthetic

质量水平

400

等级

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

管理合规性

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

蒸汽密度

4.7 (vs air)

方案

≥97.5%

表单

liquid

组成

contains IFRA restricted p-Anisaldehyde

折射率

n20/D 1.573 (lit.)

沸点

248 °C (lit.)

mp

−1 °C (lit.)

密度

1.119 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

致敏芳香化合物

no known allergens

性状检查

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

SMILES字符串

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

InChI

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

InChI key

ZRSNZINYAWTAHE-UHFFFAOYSA-N

基因信息

human ... CYP1A2(1544)

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相关类别

应用


  • 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

其他说明

天然存在：香草、茴香、八角茴香、曼越橘、黑加仑、肉桂、罗勒。

象形图

Health hazard
GHS08

警示用语：

Warning

危险声明

H361fd,H412

危险分类

Aquatic Chronic 3 - Repr. 2

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

240.8 °F - closed cup

闪点(°C)

116 °C - closed cup

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBS4355
SHBR7548
SHBQ5286
SHBP7673
SHBP7671

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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
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
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
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
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