B3000
1,4-苯二甲醇
99%
别名:
p-Phenylene dicarbinol, 对苯二甲醇, NSC 5097, 对二甲苯-α,α′-二醇, 对苯二甲醇
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关于此项目
线性分子式:
C6H4(CH2OH)2
化学文摘社编号:
分子量:
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-641-2
Beilstein/REAXYS Number:
2042077
MDL number:
产品名称
1,4-苯二甲醇, 99%
SMILES string
OCc1ccc(CO)cc1
InChI key
BWVAOONFBYYRHY-UHFFFAOYSA-N
InChI
1S/C8H10O2/c9-5-7-1-2-8(6-10)4-3-7/h1-4,9-10H,5-6H2
assay
99%
form
powder
bp
138-143 °C/1 mmHg (lit.)
mp
114-118 °C (lit.)
Quality Level
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Application
1,4-对苯二甲醇可用于制备：
- 聚（6-甲基-ε-己内酯）——聚乳酸基热塑性弹性体合成的关键中间体。
- 名为HCP−BDM（超高交联聚合物-1,4-对苯二甲醇）的高度交联聚合体，在路易斯酸存在的情况下通过Friedel−Crafts烷基化获得。
- 磺化多核芳烃树脂。
General description
1,4-苯二甲醇可用作链增长剂，用于制备二甲基硅氧烷-脲-尿烷共聚物。
wgk
WGK 3
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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A functional polyurethane based on the heterocyclic group was synthesized and its self-healing and mechanical properties were examined. To synthesize a heterocyclic polyurethane, a polyol and a heterocyclic compound with di-hydroxyl groups at both ends were blended and the blended
Polydimethylsiloxane-urea-urethane copolymers with 1, 4-benzenedimethanol as chain extender
Ho T, et al.
Macromolecules, 26, 7029-7036 (1993)
Synthesis of the sulfonated condensed polynuclear aromatic (S-COPNA) resins as strong protonic acids
Tanemura K, et al.
Tetrahedron, 67(6), 1314-1319 (2011)
Polylactide-poly (6-methyl-ε-caprolactone)-polylactide thermoplastic elastomers
Martello MT and Hillmyer M A
Macromolecules, 44(21), 8537-8545 (2011)
Tiejun Ge et al.
Polymers, 11(8) (2019-08-03)
In this experiment, terephthalyl alcohol was used as a modifier to modify phenol under both acidic and alkaline conditions to obtain modified phenols with different molecular structures. Subsequently, the modified phenols reacted with paraformaldehyde in an alkaline environment. After foaming
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