134341
对羟基联苯
97%
别名:
4-羟基联苯
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关于此项目
线性分子式:
C6H5C6H4OH
化学文摘社编号:
分子量:
170.21
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39023323
UNSPSC Code:
12352100
EC Number:
202-179-2
MDL number:
Beilstein/REAXYS Number:
1907452
产品名称
对羟基联苯, 97%
InChI key
YXVFYQXJAXKLAK-UHFFFAOYSA-N
InChI
1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H
SMILES string
Oc1ccc(cc1)-c2ccccc2
assay
97%
bp
321 °C (lit.)
mp
164-166 °C (lit.)
solubility
methanol: soluble 50 mg/mL, clear, colorless
functional group
phenyl
Quality Level
Gene Information
rat ... Ar(24208)
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Application
4-苯基苯酚可用于合成新型聚磷腈聚电解质，作为单壁碳纳米管在水中的分散剂。
General description
4-苯基苯酚经酶促聚合，聚合物发展的特点是基质辅助激光解吸电离飞行时间质谱。它是制备 4-烷基取代的酚醛树脂的中间体。
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1B
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
320.0 °F - closed cup
flash_point_c
160 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
MALDI-TOF mass spectrometry characterization of 4-alkyl substituted phenol-formaldehyde novalac type resins.
Mandal H and Hay AS.
Polymer, 38(26), 6267-6271 (1997)
Dispersion of single-walled carbon nanotubes in water with polyphosphazene polyelectrolyte.
Park HJ, et al.
Journal of Inorganic and Organometallic Polymers and Materials, 16(4), 359-364 (2006)
Peng Xu et al.
Biomacromolecules, 3(5), 889-893 (2002-09-10)
Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry is a powerful tool for polymer characterization. It has been used to understand the enzymatic polymerization of 4-phenylphenol and to monitor number average molecular weight and weight average molecular weight of the
Minoru Yamaji
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(6), 711-717 (2008-06-06)
The photochemical properties of alpha-cleavage of C-O bond in highly excited triplet states (T(n) with n>2) of p-biphenyl acetate and p-biphenyl benzoate (Me-OBP and Ph-OBP) in solution were investigated in comparison with those in the lowest excited singlet and triplet
C K Kuo et al.
Journal of pharmacobio-dynamics, 14(4), 187-193 (1991-04-01)
Species difference in glucuronidation of morphine was studied using mice, rats, guinea pigs and rabbits in vivo and in vitro. Morphine-3-glucuronide (M-3-G) and morphine-6-glucuronide (M-6-G) were determined by high-performance liquid chromatography. M-3-G was the major urinary metabolite of morphine in
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