129658
间茴香醛
97%
别名:
3-甲氧基苯甲醛
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线性分子式:
CH3OC6H4CHO
化学文摘社编号:
分子量:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-712-8
Beilstein/REAXYS Number:
606013
MDL number:
产品名称
间茴香醛, 97%
InChI key
WMPDAIZRQDCGFH-UHFFFAOYSA-N
InChI
1S/C8H8O2/c1-10-8-4-2-3-7(5-8)6-9/h2-6H,1H3
SMILES string
[H]C(=O)c1cccc(OC)c1
assay
97%
form
liquid
refractive index
n20/D 1.553 (lit.)
bp
143 °C/50 mmHg (lit.)
density
1.117 g/mL at 20 °C (lit.)
functional group
aldehyde
Quality Level
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Application
在正相硅胶色谱中，m-茴香醛可用作香兰素单-13C同位素的洗脱液。它还被用作4-（甲基亚硝基氨基）-1-（3-吡啶基）-1-丁酮（NNK）代谢的抑制剂。
General description
间茴香醛对假丝酵母菌（包耐吡咯菌株）有良好的抗真菌活性。.
间茴香醛属于苯甲醛类，可用作强效抗真菌剂和复杂芳香化合物的起始原料。
间茴香醛属于苯甲醛类，可用作强效抗真菌剂和复杂芳香化合物的起始原料。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Inhibition of metabolism of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone by dietary benzaldehydes.
M A Morse et al.
Cancer letters, 97(2), 255-261 (1995-11-06)
As part of a routine screening assay, benzaldehyde was found to inhibit 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) metabolism. Consequently, the effects of benzaldehyde and several structurally related compounds on NNK metabolism were examined in murine hepatic and pulmonary microsomes. All test compounds inhibited
Structural and spectroscopic (UV--Vis, IR, Raman, and NMR) characteristics of anisaldehydes that are flavoring food additives: A density functional study in comparison with experiments
Altun, et al.
Journal of Molecular Structure, 1128, 590-605 (2017)
Retention of sparingly soluble volatile compounds during the freeze drying of model solutions
Smyrl,et al.
Journal of Food Process Engineering, 2, 151-170 (1978)
Eliot P Botosoa et al.
Journal of chromatography. A, 1216(42), 7043-7048 (2009-09-15)
Quantitative isotopic (13)C NMR at natural abundance has been used to determine the site-by-site (13)C/(12)C ratios in vanillin and a number of related compounds eluted from silica gel chromatography columns under similar conditions. Head-to-tail isotope fractionation is observed in all
Sheikh Shreaz et al.
Microbial pathogenesis, 51(4), 277-284 (2011-06-15)
Attention has been drawn to evaluate the antifungal activity of p-anisaldehyde (1), o-anisaldehyde (2) and m-anisaldehyde (3). To put forward this approach, antifungal activity has been assessed in thirty six fluconazole-sensitive and eleven fluconazole-resistant Candida isolates. Growth and sensitivity of
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