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129658

Sigma-Aldrich

间茴香醛

97%

同義詞:

3-甲氧基苯甲醛

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About This Item

線性公式:
CH3OC6H4CHO
CAS號碼:
591-31-1
分子量：:
136.15
Beilstein:
606013
EC號碼:
209-712-8
MDL號碼:
MFCD00003361
分類程式碼代碼:
12352100
PubChem物質ID:
24847920
NACRES:
NA.22

品質等級

200

化驗

97%

形狀

liquid

折射率

n20/D 1.553 (lit.)

bp

143 °C/50 mmHg (lit.)

密度

1.117 g/mL at 20 °C (lit.)

官能基

aldehyde

SMILES 字串

[H]C(=O)c1cccc(OC)c1

InChI

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

InChI 密鑰

WMPDAIZRQDCGFH-UHFFFAOYSA-N

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相關類別

一般說明

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。

應用

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。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
WXBD6322V
WXBD3899V
WXBD1690V
WXBD1536V
WXBC5701V

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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
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
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
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. Inhibition of PO may provide a basis for novel environmentally friendly

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