Propylene carbonate (PC)


  • Product Name
  • CasNo
  • MF
  • MW
  • Content
  • Appearance
  • Packing
  • Apply
  • Propylene carbonate (PC)
  • 108-32-7
  • C4H6O3
  • 102.09
  • colourless liquid
Inquiry

Manufacturer Sells Best Quality Propylene carbonate (PC) 108-32-7 with stock

  • Molecular Formula:C4H6O3
  • Molecular Weight:102.09
  • Appearance/Colour:colourless liquid 
  • Vapor Pressure:0.13 mm Hg ( 20 °C) 
  • Melting Point:-49 °C 
  • Refractive Index:n20/D 1.421(lit.)  
  • Boiling Point:241.7 °C at 760 mmHg 
  • PKA:3.92[at 20 ℃] 
  • Flash Point:135.3 °C 
  • PSA:35.53000 
  • Density:1.169 g/cm3 
  • LogP:0.54170 

Propylene carbonate(Cas 108-32-7) Usage

Production Methods

Propylene carbonate may be prepared by the reaction of sodium bicarbonate with propylene chlorohydrin.

General Description

Propylene carbonate is a cyclic carbonate that is commonly used as a solvent and as a reactive intermediate in organic synthesis. It is being considered as a potential electrochemical solvent due to its low vapor pressure, high dielectric constant and high chemical stability.Propylene carbonate can be synthesized from propylene oxide and CO2. Optically active form of propylene carbonate can be prepared from the reaction between CO2 and racemic epoxides. Decomposition of propylene carbonate on the graphite electrode in lithium batteries results in the formation of a lithium intercalated compound.

Flammability and Explosibility

Notclassified

Pharmaceutical Applications

Propylene carbonate is used mainly as a solvent in oral and topical pharmaceutical formulations. In topical applications, propylene carbonate has been used in combination with propylene glycol as a solvent for corticosteroids. The corticosteroid is dissolved in the solvent mixture to yield microdroplets that can then be dispersed in petrolatum.Propylene carbonate has been used as a dispensing solvent in topical preparations. Propylene carbonate has also been used in hard gelatin capsules as a nonvolatile, stabilizing, liquid carrier. For formulations with a low dosage of active drug, a uniform drug content may be obtained by dissolving the drug in propylene carbonate and then spraying this solution on to a solid carrier such as compressible sugar; the sugar may then be filled into hard gelatin capsules Propylene carbonate may additionally be used as a solvent, at room and elevated temperatures, for many cellulose-based polymers and plasticizers. Propylene carbonate is also used in cosmetics.

Safety

Propylene Carbonate is listed in The Design for the Environment (DfE) Safer Chemistry Program by the EPA as a Solvent category and indicated by the Green circle, meaning the chemical has been verified to be of low concern for human and environmental health based on experimental and modeled data.In animal studies, propylene carbonate was found to cause tissue necrosis after parenteral administration.(mouse, oral): 20.7 g/kg(mouse, SC): 15.8 g/kg(rat, oral): 29 g/kg(rat, SC): 11.1 g/kg

storage

Propylene carbonate and its aqueous solutions are stable but may degrade in the presence of acids or bases, or upon heating; Store in a well-closed container in a cool, dry place.

Purification Methods

It is manufactured by reaction of 1,2-propylene oxide with CO2 in the presence of a catalyst (quaternary ammonium halide). Contaminants include propylene oxide, carbon dioxide, 1,2-and 1,3-propanediols, allyl alcohol and ethylene carbonate. It can be purified by percolation through molecular sieves (Linde 5A, dried at 350o for 14hours under a stream of argon), followed by distillation under a vacuum. [Jasinski & Kirkland Anal Chem 39 163 1967.] It can be stored over molecular sieves under an inert gas atmosphere. When purified in this way it contains less than 2ppm of water. Activated alumina and dried CaO have also been used as drying agents prior to fractional distillation under reduced pressure. It has been dried with 3A molecular sieves and distilled under nitrogen in the presence of p-toluenesulfonic acid, then redistilled and the middle fraction collected. [Beilstein 19 III/IV 1564, 19/4 V 21.]

Incompatibilities

Propylene carbonate hydrolyzes rapidly in the presence of strong acids and bases, forming mainly propylene oxide and carbon dioxide. Propylene carbonate can also react with primary and secondary amines to yield carbamates.

Regulatory Status

Included in the FDA Inactive Ingredients Database (topical ointments). Included in the Canadian List of Acceptable Nonmedicinal Ingredients.

InChI:InChI:1S/C4H6O3/c1-3-2-6-4(5)7-3/h3H,2H2,1H3

108-32-7 Relevant articles

Selective formation of polycarbonate over cyclic carbonate: Copolymerization of epoxides with carbon dioxide catalyzed by a cobalt(III) complex with a piperidinium end-capping arm

Nakano, Koji,Kamada, Toshihiro,Nozaki, Kyoko

, p. 7274 - 7277 (2006)

(Chemical Equation Presented) Sidesteppi...

New titanium catalysts containing tetrazole for cycloaddition of CO 2 to epoxides

Go, Min Jeong,Lee, Kang Mun,Oh, Chang Hwa,Kang, Yi Young,Kim, So Han,Park, Hyoung Ryun,Kim, Youngjo,Lee, Junseong

, p. 4452 - 4455 (2013)

A series of new half-sandwich titanocene...

Exploring the catalytic potential of ZIF-90: Solventless and co-catalyst-free synthesis of propylene carbonate from propylene oxide and CO2

Tharun, Jose,Mathai, George,Kathalikkattil, Amal Cherian,Roshan, Roshith,Won, Yong-Sun,Cho, Sung June,Chang, Jong-San,Park, Dae-Won

, p. 715 - 721 (2014)

Reported is the application of ZIF-90, w...

Facile synthesis of glycerol carbonate from glycerol using selenium-catalyzed carbonylation with carbon monoxide

Mizuno, Takumi,Nakai, Takeo,Mihara, Masatoshi

, p. 541 - 545 (2010)

The commercial production of glycerol ha...

Thermodynamic favorable CO2 conversion via vicinal diols and propargylic alcohols: A metal-free catalytic method

Han, Li-Hua,Li, Jing-Yuan,Song, Qing-Wen,Zhang, Kan,Zhang, Qian-Xia,Sun, Xiao-Fang,Liu, Ping

, p. 341 - 344 (2020)

Organocatalysis represents a promising f...

Homogeneous and silica-supported zinc complexes for the synthesis of propylene carbonate from propane-1,2-diol and carbon dioxide

Comerford, James W.,Hart, Sam J.,North, Michael,Whitwood, Adrian C.

, p. 4824 - 4831 (2016)

Three organozinc complexes have been syn...

Reaction of CO2 with propylene oxide and styrene oxide catalyzed by a chromium(iii) amine-bis(phenolate) complex

Dean, Rebecca K.,Devaine-Pressing, Katalin,Dawe, Louise N.,Kozak, Christopher M.

, p. 9233 - 9244 (2013)

A diamine-bis(phenolate) chromium(iii) c...

Poly(ethylene glycol): An alternative solvent for the synthesis of cyclic carbonate from vicinal halohydrin and carbon dioxide

Wang, Jing-Lun,He, Liang-Nian,Dou, Xiao-Yong,Wu, Fang

, p. 917 - 920 (2009)

Poly(ethylene glycol) (PEG) in this work...

Regioselective functionalization of glycerol with a dithiocarbamate moiety: An environmentally friendly route to safer fungicides

De Sousa, Rodolphe,Thurier, Cyril,Len, Christophe,Pouilloux, Yannick,Barrault, Joel,Jerome, Franois

, p. 1129 - 1132 (2011)

We report here a convenient pathway for ...

Adapting a Wacker-type catalyst system to the palladium-catalyzed oxidative carbonylation of aliphatic polyols

Doro, Franco,Winnertz, Patrick,Leitner, Walter,Prokofieva, Angelina,Mueller, Thomas E.

, p. 292 - 295 (2011)

Polyols, which can be obtained readily f...

An efficient catalyst system at mild reaction conditions containing rare earth metal complexes

Wu, Ya,Wang, Wen-Zhen,Wu, Yang,Duan, Yan-Shan,Zhang, Jun-Tao,Yang, Peng-Hui,Ni, Bing-Hua

, p. 1463 - 1466 (2013)

An efficient rare earthmetal complex-cat...

New synthesis of glycerol carbonate from glycerol using sulfur-assisted carbonylation with carbon monoxide

Mizuno, Takumi,Nakai, Takeo,Mihara, Masatoshi

, p. 99 - 102 (2010)

The glycerol carbonate synthesis from gl...

Propylene carbonate synthesis from propylene glycol, carbon dioxide and benzonitrile by alkali carbonate catalysts

Da Silva,Dayoub,Mignani,Raoul,Lemaire

, p. 58 - 62 (2012)

The synthesis of propylene carbonate fro...

Synthesis of cyclic carbonates from diols and CO2 catalyzed by carbenes

Bobbink, Felix D.,Gruszka, Weronika,Hulla, Martin,Das, Shoubhik,Dyson, Paul J.

, p. 10787 - 10790 (2016)

The synthesis of cyclic carbonates from ...

Electrochemical activation of carbon dioxide: Synthesis of organic carbonates

Casadei, M. Antonietta,Inesi, Achille,Rossi, Leucio

, p. 3565 - 3568 (1997)

Electrochemically activated CO2 reacts, ...

Palladium-catalyzed carbonylation of diols to cyclic carbonates

Pearson, David M.,Conley, Nicholas R.,Waymouth, Robert M.

, p. 3007 - 3013 (2011)

The catalytic alkoxycarbonylation of 1,2...

Economical synthesis of cyclic carbonates from carbon dioxide and halohydrins using K2CO3

Hirose, Takuji,Shimizu, Shinsuke,Qu, Shujie,Shitara, Hiroaki,Kodama, Koichi,Wang, Lin

, p. 69040 - 69044 (2016)

A highly simple, economical, and selecti...

An efficient and green transesterification of glycols into cyclic carbonates catalysed by KF/Ca-Mg-Al hydrotalcite

Hong, Mei,Gao, Lijing,Xiao, Guomin

, p. 679 - 681 (2014)

An efficient, convenient, and environmen...

Facile alkali-assisted synthesis of g-C3N4 materials and their high-performance catalytic application in solvent-free cycloaddition of CO2 to epoxides

Xu, Jie,Shang, Jie-Kun,Jiang, Quan,Wang, Yue,Li, Yong-Xin

, p. 55382 - 55392 (2016)

A series of graphitic carbon nitride mat...

Metal halides supported on mesoporous carbon nitride as efficient heterogeneous catalysts for the cycloaddition of CO2

Xu, Jie,Wu, Fei,Jiang, Quan,Shang, Jie-Kun,Li, Yong-Xin

, p. 77 - 83 (2015)

Abstract A series of ZnCl2/mp-C3N4 catal...

Highly active, binary catalyst systems for the alternating copolymerization of CO2 and epoxides under mild conditions

Lu, Xiao-Bing,Wang, Yi

, p. 3574 - 3577 (2004)

Excellent activity and selectivity in th...

Study of the catalytic activity of electrochemically reduced forms of phthalocyanines in the reaction of CO2 with epoxides

Magdesieva,Milovanov,Lokshin,Klemenkova,Tomilova,Butin,Zefirov

, p. 2137 - 2145 (1998)

Catalytic activity of electrochemically ...

Calcium carbide as a dehydrating agent for the synthesis of carbamates, glycerol carbonate, and cyclic carbonates from carbon dioxide

Choi, Jun-Chul,Fujitani, Tadahiro,Fukaya, Norihisa,Lin, Xiao-Tao,Sato, Kazuhiko,Yuan, Hao-Yu,Zhang, Qiao

, p. 4231 - 4239 (2020)

Carbon dioxide (CO2) is a nontoxic and i...

Pd/C: An efficient and heterogeneous protocol for oxidative carbonylation of diols to cyclic carbonate

Chavan, Sujit P.,Bhanage, Bhalchandra M.

, p. 1199 - 1202 (2014)

The present protocol involves highly eff...

Diphenyl Carbonate: A Highly Reactive and Green Carbonyl Source for the Synthesis of Cyclic Carbonates

Baral, Ek Raj,Lee, Jun Hee,Kim, Jeung Gon

, p. 11768 - 11776 (2018)

A practical, safe, and highly efficient ...

Regioselective and alternating copolymerization of carbonyl sulfide with racemic propylene oxide

Luo, Ming,Zhang, Xing-Hong,Du, Bin-Yang,Wang, Qi,Fan, Zhi-Qiang

, p. 5899 - 5904 (2013)

We report the first example of a regiore...

Propylene oxide as a dehydrating agent: Potassium carbonate-catalyzed carboxylative cyclization of propylene glycol with CO2 in a polyethylene glycol/CO2 biphasic system

Diao, Zhen-Feng,Zhou, Zhi-Hua,Guo, Chun-Xiang,Yu, Bing,He, Liang-Nian

, p. 32400 - 32404 (2016)

The synthesis of propylene carbonate (PC...

Synthesis of alkylene carbonates in ionic liquid

Kuznetsov,Pervova,Pestov

, (2013)

-

Superbase/cellulose: An environmentally benign catalyst for chemical fixation of carbon dioxide into cyclic carbonates

Sun, Jian,Cheng, Weiguo,Yang, Zifeng,Wang, Jinquan,Xu, Tingting,Xin, Jiayu,Zhang, Suojiang

, p. 3071 - 3078 (2014)

An environmentally benign catalytic syst...

Ni and Pd N-confused porphyrin complexes as catalysts for the synthesis of cyclic carbonates from epoxides and CO2

Dela Cruz, Jay-Ar B.,Ruamps, Mirko,Arco, Susan,Hung, Chen-Hsiung

, p. 7527 - 7531 (2019)

We have demonstrated the design of a nov...

Chemoselective synthesis of asymmetrical carbonate from alcohol and dimethyl carbonate catalyzed by ytterbium(III) triflate

Yu, Chuanming,Zhou, Baocheng,Su, Weike,Xu, Zhenyuan

, p. 647 - 653 (2007)

Catalyzed by ytterbium(III) triflate, as...

Biocompatible and recyclable amino acid binary catalyst for efficient chemical fixation of CO2

Yang, Zifeng,Sun, Jian,Cheng, Weiguo,Wang, Jinquan,Li, Qian,Zhang, Suojiang

, p. 6 - 9 (2014)

In this work, the cycloaddition reaction...

Zn-Mg mixed oxide as high-efficiency catalyst for the synthesis of propylene carbonate by urea alcoholysis

Zhang, Tiantian,Zhang, Bingsheng,Li, Lei,Zhao, Ning,Xiao, Fukui

, p. 38 - 41 (2015)

Zn/Mg catalysts with different atomic ra...

Copolymerization of propylene oxide with carbon dioxide catalyzed by zinc adipate

Sakharov,Il'in,Rusak,Nysenko,Klimov

, p. 1451 - 1454 (2002)

Copolymerization of carbon dioxide with ...

-

Peppel

, p. 767,770 (1958)

-

Transition metal complexes with pyrazine amine ligand: Preparation, structure and carbon dioxide copolymerization behavior

Wang, Wen-Zhen,Xu, Ya-Chao,Wang, Li,Li, Lei-Lei,Xia, Li,Jia, Xin-Gang,Lee, Gene-Hsiang,Peng, Shie-Ming

, p. 280 - 285 (2019)

Three complexes [Fe(L)2](ClO4)2 (1)、[Ni(...

Highly synergistic effect of ionic liquids and Zn-based catalysts for synthesis of cyclic carbonates from urea and diols

Cheng, Weiguo,Deng, Lili,Dong, Li,He, Hongyan,Li, Zengxi,Qian, Wei,Shi, Zijie,Su, Qian,Sun, Wenzhong

, (2020)

The development of stable and efficient ...

Effect of liophilicity of catalyst in cyclic carbonate formation by transesterification of polyhydric alcohols

Patel, Yogesh,George, Jimil,Pillai, S. Muthukumaru,Munshi, Pradip

, p. 1056 - 1060 (2009)

The effect of catalyst liophilicity is s...

Self-assembled bimetallic aluminum-salen catalyst for the cyclic carbonates synthesis

Abboud, Khalil A.,Hahm, Hyungwoo,Hong, Sukwon,Kim, Seyong,Park, Jongwoo,Seong, Wooyong

, (2021)

Bimetallic bis-urea functionalized salen...

Catalytic synthesis of propylene carbonate from propylene oxide and carbon dioxide in the presence of rhodium complexes modified with organophosphorus ligands and chitosan

Korosteleva,Markova,Kolesnichenko,Ezhova,Khadzhiev,Trukhmanova

, p. 412 - 417 (2013)

The reaction between CO2 and propylene o...

CO2 activation and promotional effect in the oxidation of cyclic olefins over mesoporous carbon nitrides

Ansari, Mohd Bismillah,Min, Byung-Hoon,Mo, Yong-Hwan,Park, Sang-Eon

, p. 1416 - 1421 (2011)

Mesoporous carbon nitrides (MCN) were pr...

THE REACTION OF 1,3,2-DIOXASTANNOLANS WITH DIACYL CHLORIDES: DECARBONYLATION IN THE REACTION WITH OXALYL CHLORIDE

Davies, Alwyn G.,Hua-De, Pan,Hawari, Jalal A. -A.

, p. 251 - 260 (1983)

2,2-Dibutyl-1,3,2-dioxastannolans react ...

Controlled synthesis of asymmetric dialkyl and cyclic carbonates using the highly selective reactions of imidazole carboxylic esters

Rannard, Steve P.,Davis, Nicola J.

, p. 933 - 936 (1999)

(equation presented) A new highly select...

One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis

Jia, Fan,Chen, Xiaoyu,Zheng, Yan,Qin, Yusheng,Tao, Youhua,Wang, Xianhong

, p. 8504 - 8507 (2015)

One-pot synthesis of well-defined bio-re...

Synthesis of 5-membered cyclic carbonates by oxidative carbonylation of 1,2-diols promoted by copper halides

Giannoccaro, Potenzo,Casiello, Michele,Milella, Antonella,Monopoli, Antonio,Cotugno, Pietro,Nacci, Angelo

, p. 162 - 171 (2012)

Copper halides, CuX2 (X = Cl, Br), promo...

Microwave-assisted one pot-synthesis of amino acid ionic liquids in water: Simple catalysts for styrene carbonate synthesis under atmospheric pressure of CO2

Roshan, Kuruppathparambil Roshith,Jose, Tharun,Kim, Dongwoo,Cherian, Kathalikkattil Amal,Park, Dae Won

, p. 963 - 970 (2014)

A novel variety of ionic liquids based o...

One-pot conversion of CO2 and glycerol to value-added products using propylene oxide as the coupling agent

Ma, Jun,Song, Jinliang,Liu, Huizhen,Liu, Jinli,Zhang, Zhaofu,Jiang, Tao,Fan, Honglei,Han, Buxing

, p. 1743 - 1748 (2012)

The effective conversion of carbon dioxi...

Versatile boiler ash containing potassium silicate for the synthesis of organic carbonates

Indran, Vidhyaa Paroo,Haji Saud, Anisah Sajidah,Maniam, Gaanty Pragas,Yusoff, Mashitah Mohd.,Taufiq-Yap, Yun Hin,Ab. Rahim, Mohd Hasbi

, p. 34877 - 34884 (2016)

In this study, boiler ash containing pot...

Novel chromium (III) complexes with N4-donor ligands as catalysts for the coupling of CO2 and epoxides in supercritical CO2

Cuesta-Aluja, Laia,Djoufak, Mary,Aghmiz, Ali,Rivas, Raquel,Christ, Lorraine,Masdeu-Bultó, Anna M.

, p. 161 - 170 (2014)

New neutral and cationic chromium(III) c...

Direct synthesis of polycarbonate diols from atmospheric flow CO2and diols without using dehydrating agents

Gu, Yu,Nakagawa, Yoshinao,Nakao, Kenji,Suzuki, Kimihito,Tamura, Masazumi,Tomishige, Keiichi

, p. 5786 - 5796 (2021/08/23)

Polymer synthesis with CO2 as a C1 chemi...

Cross-linked, porous imidazolium-based poly(ionic liquid)s for CO2capture and utilisation

Al-Maythalony, Bassem A.,Al-Qaisi, Feda'a M.,Assaf, Khaleel I.,Eftaiha, Ala'a F.,Hasan, Areej K.,Melhem, Maryam E.,Qaroush, Abdussalam K.,Usman, Muhammad

supporting information, p. 16452 - 16460 (2021/09/28)

CO2is the most influential greenhouse ga...

METHOD FOR SUSTAINABLE CHEMICAL FIXATION OF CO2

-

Page/Page column 16, (2021/02/19)

A method for sustainable fixation of CO2...

Acylamino-bridged hexacarboxylic acid ligand, metal organic framework material, and preparation method and application of acylamino-bridged hexacarboxylic acid ligand and metal organic framework material

-

Paragraph 0119-0122; 0128-0130, (2021/05/12)

The invention relates to the field of me...

108-32-7 Process route

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

methyloxirane
75-56-9,16033-71-9

methyloxirane

1,2-propylene cyclic carbonate
108-32-7

1,2-propylene cyclic carbonate

propylene glycol
57-55-6,63625-56-9

propylene glycol

Conditions
Conditions Yield
tetra-n-butylphosphonium chloride; at 180 ℃; for 4h; under 15001.5 - 37503.8 Torr; Product distribution / selectivity; Gas phase;
93.4%
0.3%
tetraethylphosphonium bromide; at 180 ℃; for 4h; under 15001.5 - 37503.8 Torr; Product distribution / selectivity; Gas phase;
92.7%
0.5%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; cellulose; at 120 ℃; for 2h; under 15001.5 Torr; Reagent/catalyst; Temperature; Catalytic behavior; Autoclave; Green chemistry;
90%
methyl(tributyl)phosphonium iodide; at 180 ℃; for 4h; under 15001.5 - 37503.8 Torr; Product distribution / selectivity; Gas phase;
75.1%
0.3%
tetra-n-butylphosphonium iodide; at 180 ℃; for 4h; under 15001.5 - 37503.8 Torr; Product distribution / selectivity; Gas phase;
72%
0.4%
tribenzyl-methyl-phosphonium; bromide; at 180 ℃; for 4h; under 15001.5 - 37503.8 Torr; Product distribution / selectivity; Gas phase;
70.3%
0.2%
tetrabutyl phosphonium bromide; at 180 ℃; for 4h; under 15001.5 - 37503.8 Torr; Product distribution / selectivity; Gas phase;
64.8%
0.3%
With C20H24ClCrN4(2+)*2Cl(1-); tetra-(n-butyl)ammonium iodide; at 100 ℃; for 0.5h; under 127513 Torr; Catalytic behavior; Supercritical conditions; Autoclave;
60 %Chromat.
With rhodium(III) chloride; hydrogen; In dimethyl sulfoxide; at 140 ℃; for 16.5h; under 37503.8 Torr; Reagent/catalyst; Kinetics; Autoclave;
With bis(imidazolate-2-carboxyaldehyde)zinc(II); In neat (no solvent); at 120 ℃; for 8h; under 9000.9 Torr; Pressure; Temperature; Catalytic behavior; Autoclave;
81 %Chromat.
With zinc(II) iodide; at 140 ℃; for 6h; under 15001.5 Torr; Reagent/catalyst; Temperature; Overall yield = 89.5 %; Catalytic behavior; Autoclave;
With water; In acetonitrile; at 40 ℃; for 1h; under 3750.38 Torr; Pressure; Reagent/catalyst; Solvent; Temperature; Autoclave;
methanol
67-56-1

methanol

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

methyloxirane
75-56-9,16033-71-9

methyloxirane

1,2-propylene cyclic carbonate
108-32-7

1,2-propylene cyclic carbonate

propylene glycol
57-55-6,63625-56-9

propylene glycol

1-methoxy-2-propanol
107-98-2

1-methoxy-2-propanol

2-methoxypropanol
1589-47-5

2-methoxypropanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

Conditions
Conditions Yield
With 6,7,9,10,12,13,20,21-octahydrodibenzo[b,h][1,4,7,10,13,16]hexaoxacyclooctadecine; potassium chloride; at 130 ℃; for 8h; under 15001.5 Torr; Reagent/catalyst; Autoclave; High pressure;
13.2%
69.2%
12.5%
With 6,7,9,10,12,13,20,21-octahydrodibenzo[b,h][1,4,7,10,13,16]hexaoxacyclooctadecine; potassium bromide; at 130 ℃; for 8h; under 15001.5 Torr; Reagent/catalyst; Autoclave; High pressure;
12.5%
62.9%
14.4%
With potassium bromide; at 130 ℃; for 8h; under 15001.5 Torr; Autoclave; High pressure;
5.8%
44.1%
6.7%
With 6,7,9,10,12,13,20,21-octahydrodibenzo[b,h][1,4,7,10,13,16]hexaoxacyclooctadecine; potassium chloride; at 130 ℃; for 8h; under 15001.5 Torr; Autoclave; High pressure;
23%
41.7%
29.8%
With potassium carbonate; at 140 ℃; for 6h; Supercritical conditions; Green chemistry;
33.8%
20.3%
36.2%
With potassium carbonate; at 160 ℃; for 6h; Supercritical conditions; Green chemistry;
36.4%
19.9%
33.9%
With potassium chloride; at 130 ℃; for 8h; under 15001.5 Torr; Autoclave; High pressure;
7.8%
35.9%
7.8%
With Zn4O(1,4-benzenedicarboxylate)3; potassium carbonate; potassium iodide; at 130 ℃; for 4h; under 30003 Torr; Autoclave;
70 %Chromat.
15.3 %Chromat.
17.3 %Chromat.

108-32-7 Upstream products

  • 57-55-6
    57-55-6

    propylene glycol

  • 598-99-2
    598-99-2

    Methyl trichloroacetate

  • 15719-64-9
    15719-64-9

    methylammonium carbonate

  • 127-00-4
    127-00-4

    1-Chloro-2-propanol

108-32-7 Downstream products

  • 1133-80-8
    1133-80-8

    2-bromo-9H-fluorene

  • 2051-98-1
    2051-98-1

    5-bromoacenaphthene

  • 106-38-7
    106-38-7

    para-bromotoluene

  • 95-46-5
    95-46-5

    2-methylphenyl bromide

*Product Name:
*Email:
*Description:
*Code:
Contact Now