I19209
间苯二甲酸
99%
别名:
1,3-苯二甲酸
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关于此项目
线性分子式:
C6H4-1,3-(CO2H)2
化学文摘社编号:
分子量:
166.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-506-4
Beilstein/REAXYS Number:
1909332
MDL number:
Assay:
99%
InChI key
QQVIHTHCMHWDBS-UHFFFAOYSA-N
InChI
1S/C8H6O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H,(H,9,10)(H,11,12)
SMILES string
OC(=O)c1cccc(c1)C(O)=O
assay
99%
autoignition temp.
1198 °F
mp
341-343 °C (lit.)
Quality Level
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Application
间苯二甲酸可作为制备以下物质的反应物：
它也可用作合成以下物质的配体：
- 通过与间苯二胺的热固相聚合反应制备的聚(间苯二甲酰间苯二胺）。
它也可用作合成以下物质的配体：
- 通过水热和声化学工艺制备的金属配位聚合物。
- 间苯二甲酸-锆(IV)纳米复合材料,其可用作热分解法制备结晶四方ZrO2 的前体。
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Sonochemical synthesis of two nano-sized nickel (II) coordination polymers derived from flexible bis (benzimidazole) and isophthalic acid ligands
Li Jun-Xuan, et al.
Polyhedron, 160, 92-100 (2019)
Jörg Lincke et al.
Inorganic chemistry, 51(14), 7579-7586 (2012-07-04)
An isomorphous series of 10 microporous copper-based metal-organic frameworks (MOFs) with the general formulas (∞)(3)[{Cu(3)(μ(3)-OH)(X)}(4){Cu(2)(H(2)O)(2)}(3)(H-R-trz-ia)(12)] (R = H, CH(3), Ph; X(2-) = SO(4)(2-), SeO(4)(2-), 2 NO(3)(2-) (1-8)) and (∞)(3)[{Cu(3)(μ(3)-OH)(X)}(8){Cu(2)(H(2)O)(2)}(6)(H-3py-trz-ia)(24)Cu(6)]X(3) (R = 3py; X(2-) = SO(4)(2-), SeO(4)(2-) (9, 10)) is presented
Bo Xiao et al.
Nature chemistry, 1(4), 289-294 (2009-07-01)
Metal organic frameworks (MOFs) are among the most exciting materials discovered recently, attracting particular attention for their gas-adsorption and -storage properties. Certain MOFs show considerable structural flexibility in response to various stimuli. Although there are several examples of 'breathing' MOFs
Preparation and characterization of tetragonal zirconium oxide nanocrystals from isophthalic acid-zirconium (IV) nanocomposite as a new precursor
Ranjbar M, et al.
International Journal of Nanoscience, 8(4), 191-196 (2012)
Yue-Xiu Si et al.
International journal of biological macromolecules, 48(4), 700-704 (2011-03-05)
Using inhibition kinetics and computational simulation, we studied the reversible inhibition of tyrosinase by isophthalic acid (IPA). IPA inhibited tyrosinase in a complex manner with K(i)=17.8 ± 1.8mM. Measurements of intrinsic and ANS-binding fluorescence showed that IPA induced no changes
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