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形狀
crystalline
自燃溫度
959 °F
顏色
dark gray to brown
bp
240-243 °C (lit.)
mp
56-59 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
COc1ccc(N)cc1
InChI
1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
InChI 密鑰
BHAAPTBBJKJZER-UHFFFAOYSA-N
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产品编号
说明
价格
訊號詞
Danger
危險分類
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Carc. 1B - STOT RE 2
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
251.6 °F - closed cup
閃點（°C）
122 °C - closed cup
K Héberger et al.
Lipids, 34(1), 83-92 (1999-04-03)
Decomposition of hydroperoxides in sunflower oil under strictly oxygen-free conditions was followed by measuring peroxide values against time, absorbance values at 232 and 268 nm, para-anisidine values, and by quantitative analyses of volatile products using various additives. The results were
Francesco Caponio et al.
Journal of food science, 74(9), C701-C706 (2010-05-25)
An experimental investigation was carried out to evaluate the influence of processing and storage time on the lipidic fraction of taralli. The data obtained pointed out that the kneading phase caused a significant increase of the oxidized triacylglycerols and triacylglycerol
C Meier et al.
Carcinogenesis, 12(9), 1633-1640 (1991-09-01)
We report here on the conformational analysis of C8-arylamine nucleoside and nucleotide adducts of the borderline carcinogens 4-methylaniline and 4-methoxyaniline. The non-phosphorylated adducts show anti conformation of the glycosidic link, while the corresponding 5'-phosphorylated adducts have a syn conformation. All
James S Harvey et al.
Mutagenesis, 20(1), 51-56 (2005-01-27)
The pH 6.7 Syrian hamster embryo (SHE) cell morphological transformation assay is a short-term in vitro test that has been used to predict rodent carcinogenicity. Previous reports have indicated that the SHE assay has an overall concordance of approximately 80%
Yujiro Hayashi et al.
Nature protocols, 2(1), 113-118 (2007-04-03)
This protocol describes a procedure for the synthesis of syn-beta-amino alpha-substituted aldehydes, versatile intermediates in synthetic organic chemistry, via asymmetric, direct, one-pot, three-component, cross-Mannich reaction of two different aldehydes. The reaction consists of two steps; one is the formation of
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