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
Assay:
97%
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。
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。
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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)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 368946-1G | 04061826258088 |
| 368946-5G | 04061833313985 |
| 134341-5G | 04061838729996 |
| 134341-100G | 04061838729989 |