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Merck

117552

Sigma-Aldrich

邻甲基苯甲醛

97%

别名:

2-甲基苯甲醛

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About This Item

线性分子式:
CH3C6H4CHO
CAS号:
分子量:
120.15
Beilstein:
605841
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

包含

0.1% Hydroquinone as stabilizer

折射率

n20/D 1.546 (lit.)

bp

199-200 °C (lit.)

密度

1.039 g/mL at 20 °C
1.039 g/mL at 25 °C (lit.)

SMILES 字串

[H]C(=O)c1ccccc1C

InChI

1S/C8H8O/c1-7-4-2-3-5-8(7)6-9/h2-6H,1H3

InChI 密鑰

BTFQKIATRPGRBS-UHFFFAOYSA-N

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相关类别

一般說明

甲苯甲醛通过阳光直接光解,在大气中降解

應用

通过加入磷酸,通过 HPLC 测定邻甲苯甲醛的烯基-2,4-二硝基苯腙

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - 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)

170.6 °F

閃點(°C)

77 °C

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Measurement of acid-catalyzed isomerization of unsaturated aldehyde-2, 4-dinitrophenylhydrazone derivatives by high-performance liquid chromatography analysis.
Uchiyama S, et al.
Analytica Chimica Acta, 523(2), 157-163 (2004)
C J Cros et al.
Indoor air, 22(1), 43-53 (2011-07-23)
The health effects associated with exposure to ozone range from respiratory irritation to increased mortality. In this paper, we explore the use of three green building materials and an activated carbon (AC) mat that remove ozone from indoor air. We
Grainne M Clifford et al.
Environmental science & technology, 45(22), 9649-9657 (2011-10-20)
The photolysis of o-tolualdehyde by natural sunlight has been investigated at the large outdoor European Photoreactor (EUPHORE) in Valencia, Spain. The photolysis rate coefficient was measured directly under different solar flux levels, with values in the range j(o-tolualdehyde) = (1.62-2.15)
Qing-Xi Chen et al.
Journal of enzyme inhibition and medicinal chemistry, 18(6), 491-496 (2004-03-11)
The inhibition kinetics on the diphenolase activity of mushroom tyrosinase by some alkylbenzaldehydes has been investigated. The results show that the alkylbenzaldehydes assayed can lead to reversible inhibition to the enzyme; o-tolualdehyde and m-tolualdehyde are mixed-type inhibitors and p-alkylbenzaldehydes are
K Watanabe et al.
Drug metabolism and disposition: the biological fate of chemicals, 23(2), 261-265 (1995-02-01)
Mouse hepatic microsomal enzymes catalyzed the oxidation of o-, m-, and p-tolualdehydes, intermediate metabolites of xylene, to the corresponding toluic acids. Cofactor requirement for the catalytic activity indicates that the microsomes contain NAD- and NADPH-dependent enzymes for this reaction. GC/MS

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