推荐产品
蒸汽密度
3.8 (vs air)
品質等級
蒸汽壓力
1 mmHg ( 75 °C)
10 mmHg ( 118.3 °C)
產品線
BioReagent
化驗
≥99%
形狀
powder
技術
cell culture | plant: suitable
顏色
white to faint beige
bp
245 °C (lit.)
mp
100-103 °C (lit.)
溶解度
water: 50 mg/mL, clear, colorless to faintly yellow
儲存溫度
room temp
SMILES 字串
Oc1ccccc1O
InChI
1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H
InChI 密鑰
YCIMNLLNPGFGHC-UHFFFAOYSA-N
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注意
暴露于空气和光线中时可能变色。
訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Carc. 1B - Eye Dam. 1 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
閃點（°F）
260.6 °F - closed cup
閃點（°C）
127 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
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Proceedings of the National Academy of Sciences of the United States of America, 109(52), 21444-21449 (2012-12-14)
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New graphene-silk peptide (Gr-SP) nanosheets were prepared and successfully fabricated with tyrosinase (Tyr) as a novel biosensor for the determination of phenolic compounds. The Gr-SP nanosheets were fully characterized with transmission electron microscopy, x-ray diffraction, x-ray photoelectron spectroscopy, UV/Vis and
R D Irons
Journal of toxicology and environmental health, 16(5), 673-678 (1985-01-01)
Occupational exposure to benzene has long been associated with toxicity to the blood and bone marrow, including lymphocytopenia, pancytopenia, aplastic anemia, acute myelogenous leukemia, and possibly lymphoma. A variety of studies have established that benzene itself is not the toxic
Myung-Hyun Ryou et al.
Advanced materials (Deerfield Beach, Fla.), 25(11), 1571-1576 (2013-01-03)
Conjugation of mussel-inspired catechol groups to various polymer backbones results in materials suitable as silicon anode binders. The unique wetness-resistant adhesion provided by the catechol groups allows the silicon nanoparticle electrodes to maintain their structure throughout the repeated volume expansion
Jacques Poupaert et al.
Current medicinal chemistry, 12(7), 877-885 (2005-04-28)
The 2(3H)-benzoxazolone heterocycle and its bioisosteric surrogates (such as 2(3H)-benzothiazolinone, benzoxazinone, etc.) have received considerable attention from the medicinal chemists owing to their capacity to mimic a phenol or a catechol moiety in a metabolically stable template. These heterocycles and
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