26099-09-2

  • Product Name:Polymaleic acid
  • Molecular Formula:(C4H4O4)n
  • Purity:99%
  • Molecular Weight:116.073
Inquiry

Product Details

Appearance:orange transparent liquid

Purity:99%

Offer Chemical Raw Material Polymaleic acid 26099-09-2 In Stock

  • Molecular Formula:C4H4O4
  • Molecular Weight:116.073
  • Appearance/Colour:orange transparent liquid 
  • Flash Point:95 °C 
  • PSA:74.60000 
  • Density:1.18 (48% aq.) 
  • LogP:-0.28820 

26099-09-2 Relevant articles

Liquid hydrogenation of maleic anhydride with Pd/C catalyst at low pressure and temperature in batch reactor

Kim, Ji Sun,Baek, Jae Ho,Ryu, Young Bok,Hong, Seong-Soo,Lee, Man Sig

, p. 290 - 294 (2015)

Succinic acid (SA) produced from hydroge...

Catalyst for catalytic oxidation of furfural to prepare maleic acid and application thereof

-

Page/Page column 10-12, (2022/02/10)

A catalyst for catalytic oxidation of fu...

Ordered mesoporous carbon as an efficient heterogeneous catalyst to activate peroxydisulfate for degradation of sulfadiazine

Cao, Di,Chen, Fan,Cheng, Hao,Huang, Cong,Li, Zhi-Ling,Liang, Bin,Nan, Jun,Sun, Kai,Wang, Ai-Jie

supporting information, (2022/01/26)

Catalytic potential of carbon nanomateri...

Electrochemical Strategy for the Simultaneous Production of Cyclohexanone and Benzoquinone by the Reaction of Phenol and Water

Wu, Ruizhi,Meng, Qinglei,Yan, Jiang,Liu, Huizhen,Zhu, Qinggong,Zheng, Lirong,Zhang, Jing,Han, Buxing

, p. 1556 - 1571 (2022/02/01)

Cyclohexanone and benzoquinone are impor...

Direct catalytic benzene hydroxylation under mild reaction conditions by using a monocationic μ-nitrido-bridged iron phthalocyanine dimer with 16 peripheral methyl groups

Tanaka, Kentaro,Teoh, Chee-Ming,Toyoda, Yuka,Yamada, Yasuyuki

supporting information, p. 955 - 958 (2022/02/07)

Direct catalytic hydroxylation of benzen...

26099-09-2 Process route

sulfuric acid
7664-93-9

sulfuric acid

p-benzoquinone
106-51-4

p-benzoquinone

formic acid
64-18-6

formic acid

DL-tartaric acid
133-37-9,138508-61-9

DL-tartaric acid

maleic acid
110-16-7,26099-09-2

maleic acid

Conditions
Conditions Yield
Electrolysis;
nitrobenzene
98-95-3,26969-40-4

nitrobenzene

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

malonic acid
141-82-2

malonic acid

1,2-dihydroxy-4-nitrobenzene
3316-09-4

1,2-dihydroxy-4-nitrobenzene

meta-nitrophenol
554-84-7

meta-nitrophenol

oxalic acid
144-62-7,97993-78-7

oxalic acid

maleic acid
110-16-7,26099-09-2

maleic acid

hydroquinone
123-31-9,8027-02-9

hydroquinone

p-benzoquinone
106-51-4

p-benzoquinone

2-hydroxynitrobenzene
88-75-5,78813-12-4

2-hydroxynitrobenzene

phenol
108-95-2,27073-41-2

phenol

Conditions
Conditions Yield
With ozone; In water; at 24.84 ℃; Mechanism; Ultrasound irradiation;

26099-09-2 Upstream products

  • 109-99-9
    109-99-9

    tetrahydrofuran

  • 110-89-4
    110-89-4

    piperidine

  • 110-86-1
    110-86-1

    pyridine

  • 141-82-2
    141-82-2

    malonic acid

26099-09-2 Downstream products

  • 51112-81-3
    51112-81-3

    endo, cis-7-oxabicyclo<2.2.1>hept-5-ene-2,3-dicarboxylic acid

  • 28871-62-7
    28871-62-7

    7-Oxa-bicyclo-<2.2.1>-hept-5-en-2,3-exo,exo-dicarbonsaeure

  • 6280-78-0
    6280-78-0

    (+/-)-6t-Brom-5c-hydroxy-7-oxa-(1rH.4cH)-bicyclo<2.2.1>heptan-2c.3c-dicarbonsaeure-3-lacton

  • 6280-79-1
    6280-79-1

    (+/-)-5endo,6exo-dibromo-7-oxa-norbornane-2exo,3exo-dicarboxylic acid