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4525-33-1

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4525-33-1 Usage

Description

Dimethyl dicarbonate (DMDC), also known as Viguolin, is a kind of fruit juice beverage preservative (INS No. 242) that is allowed to be used in my country's food additive use standards. Under normal or even low temperature conditions, DMDC has a strong ability to kill many contaminating bacteria in fruit juice drinks, and its antiseptic effect is closely related to the modification and inactivation of key enzyme proteins in the bacteria by DMDC. Compared with other physical sterilization technologies, the use of DMDC is low in cost, simple and safe to operate, and does not affect the taste, smell and color of the product. It has become one of the hotspots in the research of emerging non-thermal sterilization technologies.

Mechanism of action

Dimethyl dicarbonate has been approved by FDA for use as a yeast inhibitor in bottled wines ( FR Oct. 21 , 1988 ) .It is highly reactive and can react chemically with a variety of reactive groups (such as sulfhydryl, hydroxyl, amino and carboxyl). Among them, the researchers focused on the characteristics of the reaction between pyrocarbonate compounds and enzyme proteins. The results show that in the reaction between enzyme protein and pyrocarbonate compounds, the imidazole group in histidine residues in the enzyme protein is mainly involved in the reaction to form methyl (or ethyl) oxyformyl imidazole group. In addition, studies have also found that many enzymes (such as bovine brain tissue succinate semialdehyde reductase, nucleic acid hydrolase, alcohol dehydrogenase, etc.) have been modified by pyrocarbonate compounds, their enzyme activity has been significantly reduced, and the enzyme activity has decreased and the enzyme activity has decreased. The degree of histidine modification in the protein has a significant correlation.

Uses

Different sources of media describe the Uses of 4525-33-1 differently. You can refer to the following data:
1. Dimethyl dicarbonate (DMDC), a chemical used to combat brettanomyces in wine, is classified as an additive.DMDC is allowed for the preservation of nonalcoholic flavored drinks, alcohol-free wine, and liquid-tea concentrate in ingoing amounts up to 250 mg/L.Because of its reactivity to nucleophilic groups present in proteins, it easily binds to these, which, in the case of enzymes, leads to inactivation of these and hence to inactivation of microorganisms.150In an aqueous medium, it undergoes complete hydrolysis to methanol and carbon dioxide within a few hours. The EC Directive provides a remark that dimethyl dicarbonate residues are not detectable in drinks.
2. Dimethyl Dicarbonate(DMDC) is a microbial control agent used in wine; ready-to-drink teas; nonjuice-containing beverages; carbonated,dilute beverages containing juice, fruit flavor or both with the juice content not exceeding 50%.Dimethyl Dicarbonate has been commonly used as a antimicrobial agent for a broad spectrum of microorganisms. The primary target microorganisms of DMDC are yeasts, including Saccharomyces, Zygosaccharomyces, Rhodotorula, Candida, Pichia, Torulopsis, Torula, Endomyces, Kloeckera and Hansenula. DMDC is also bactericidal to a number of species including Acetobacter pasteurianus, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, several Lactobacillus species and Pediococcus cerevisiae DMDC has also been shown to be bactericidal against Escherichia coli O157:H7.The antimicrobial effect of DMDC results from the deactivation of microbial enzymes, mainly through reaction with protein imidazole and amine groups, leading to the destruction of the microorganisms. The remaining unreacted DMDC breaks down rapidly into methanol and carbon dioxide. The DMDC activity is based on the hydrolysis rate. Hydrolysis occurs when DMDC reacts with water and the rate is dependent on the temperature of the beverage or wine. It takes about four hours at 10°C (50°F) or two hours at 20°C (68°F) for DMDC completely breaking down.

Preparation

In a 2000ml reaction flask, add 400g methyl chloroformate (industrial grade), 400ml dichloromethane, add 143.82g dodecyldimethylbenzylammonium chloride, stir and cool to 5-15°C, Add 1166gl 4% sodium hydroxide aqueous solution dropwise. After the addition is complete, let stand for layering. Discard the water layer. Add 32g 85% sulfuric acid to the organic layer. Stir for 1.5 hours at room temperature. Separate the layers. Add anhydrous magnesium sulfate to dry the organic layer and filter. , Then vacuum distillation, first remove the solvent, and then collect the 200Pa, 30°C -35°C distillate to obtain 232g of colorless liquid product dimethyl dicarbonate, yield 81.9%, freezing point 17°C, GC purity 99.9%.

Safety Profile

Dimethyl dicarbonate (Velcorinor DMDC) is now used as a preservative in many countries but its toxicity requires the use of special dispensing equipment. Dimethyl dicarbonate decom-poses to CHgOH and CO2 in a product and its maximum rate of addition is typi-cally 0.025 wt%.DMDC is used in the beverage industry for supplemental microbial control in beverages during the final stages of filling. It is added to beverages, whose viable microorganism load was previously reduced by other technologies, immediately prior to bottling, canning, or other forms of final packaging. To ensure its safe use, the agency set the maximum amount of DMDC that may be added to food at 250 parts per million (ppm). DMDC is currently approved under §?172.133(b)(1) and (b)(2) as an inhibitor of yeast in various beverages under normal circumstances of bottling or canning where the viable yeast count has been reduced to 500 per milliliter (mL) or less by current good manufacturing practices. DMDC is also approved under §?172.133(b)(3) and (b)(4) as an inhibitor of yeast in additional beverages. During its review of the subject petition, FDA found that restrictions given in paragraphs (b)(1) and (b)(2) were inadvertently omitted from paragraphs (b)(3) and (b)(4).https://www.federalregister.gov/documents/2001/03/07/01-5511/food-additives-permitted-for-direct-addition-to-food-for-human-consumption-dimethyl-dicarbonate

Chemical Properties

Dimethyl dicarbonate (DMDC) is a colourless liquid with a slightly pungent aroma. It is primarily used as a beverage preservative, processing aid, or sterilant (Enumber 242). The application of DMDC is particularly useful when wine needs to be sterilized but cannot be sterile filtered, pasteurized, or sulfured. DMDC is also used to stabilize non-alcoholic beverages such as carbonated or non-carbonated juice beverages, isotonic sports beverages, iced teas, and flavored waters.

Purification Methods

Dissolve it in Et2O, shake this with a small volume of 0.1N HCl, dry Et2O with Na2SO4 and distil in in vacuo below 100o to give a clear liquid. It decomposes to CO2 and dimethyl carbonate on heating at 123-149o. It is readily hydrolysed by H2O and is a yeast inhibitor and an IRRITANT. [Brysov et al. J Org Chem USSR 10 2551 1974, Boehm & Mehta Chem Ber 71 1797 1938, Beilstein 3 IV 17.]

Check Digit Verification of cas no

The CAS Registry Mumber 4525-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4525-33:
(6*4)+(5*5)+(4*2)+(3*5)+(2*3)+(1*3)=81
81 % 10 = 1
So 4525-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O5/c1-7-3(5)9-4(6)8-2/h1-2H3

4525-33-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl dicarbonate

1.2 Other means of identification

Product number -
Other names DMPC Dimethyl pyrocarbonate Pyrocarbonic acid dimethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4525-33-1 SDS

4525-33-1Synthetic route

methyl chloroformate
79-22-1

methyl chloroformate

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

Conditions
ConditionsYield
With sodium hydroxide; triisooctyl amine In water; toluene at 17℃; for 1.25h; Product distribution / selectivity; Alkaline conditions;91%
With sodium hydroxide; triisooctyl amine In water; toluene at 17℃; for 1.25h; Product distribution / selectivity;91%
With sodium hydroxide; tridodecylamine In water; toluene at 5 - 15℃; for 1.16667h; Product distribution / selectivity; Alkaline conditions;85%
With sodium hydroxide; tridodecylamine In water; toluene at 5 - 15℃; for 1.16667h; Product distribution / selectivity;85%
With water; sodium hydroxide In toluene at 17℃; for 0.333333h; Reagent/catalyst; Temperature;
methyl chloroformate
79-22-1

methyl chloroformate

sodium-salt of carbonic acid monomethyl ester

sodium-salt of carbonic acid monomethyl ester

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

piperidin-3-ol hydrochloride
64051-79-2

piperidin-3-ol hydrochloride

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

3-hydroxypiperidine-1-carboxylic acid methyl ester
80613-04-3

3-hydroxypiperidine-1-carboxylic acid methyl ester

Conditions
ConditionsYield
With TEA In dichloromethane at 0 - 20℃;100%
With triethylamine In dichloromethane at 0 - 20℃;
2-furanoic acid
88-14-2

2-furanoic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

2-furoic acid methyl ester
611-13-2

2-furoic acid methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;99%
With dmap In tetrahydrofuran for 88h;97%
N-tert-butoxycarbonyl-L-phenylalanine
13734-34-4

N-tert-butoxycarbonyl-L-phenylalanine

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

(S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester
51987-73-6

(S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester

Conditions
ConditionsYield
With dmap In tetrahydrofuran for 0.25h;99%
dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

10-methoxycarbonyl-10-desacetylbaccatin III

10-methoxycarbonyl-10-desacetylbaccatin III

Conditions
ConditionsYield
With cerium(III) chloride In tetrahydrofuran at 25℃; for 3h;98%
With cerium(III) chloride In tetrahydrofuran at 25℃; for 3h;98%
With cerium(III) chloride In tetrahydrofuran at 25℃; for 3h; Under N2;98%
cerium(III) chloride In tetrahydrofuran at 25℃; for 3h;98%
dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

4-nitro-benzoic acid
62-23-7

4-nitro-benzoic acid

4-nitrobenzoic acid methyl ester
619-50-1

4-nitrobenzoic acid methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;98%
With 2,6-dimethylpyridine; fac-tris(2-phenylpyridinato-N,C2')iridium(III) In N,N-dimethyl-formamide at 20℃; for 48h; Sealed tube; Inert atmosphere; Irradiation;
dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

7,8-diamino-10-methylsulfanyl-decanoic acid methyl ester dihydrochloride

7,8-diamino-10-methylsulfanyl-decanoic acid methyl ester dihydrochloride

7,8-bis-methoxycarbonylamino-10-methylsylfanyl-decanoic acid methyl ester
681848-51-1

7,8-bis-methoxycarbonylamino-10-methylsylfanyl-decanoic acid methyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 3.5h;98%
cis-(1S,3R)-3-<(N-Boc-L-alanyl)amino>cyclopent-4-enol
160057-16-9

cis-(1S,3R)-3-<(N-Boc-L-alanyl)amino>cyclopent-4-enol

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

Carbonic acid (1S,4R)-4-((S)-2-tert-butoxycarbonylamino-propionylamino)-cyclopent-2-enyl ester methyl ester
177990-92-0

Carbonic acid (1S,4R)-4-((S)-2-tert-butoxycarbonylamino-propionylamino)-cyclopent-2-enyl ester methyl ester

Conditions
ConditionsYield
With dmap In dichloromethane97%
1-(tert-butoxycarbonyl)-L-proline
15761-39-4

1-(tert-butoxycarbonyl)-L-proline

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

(S)-N-(tert-butoxycarbonyl)proline methyl ester
59936-29-7

(S)-N-(tert-butoxycarbonyl)proline methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;97%
With dmap In tetrahydrofuran82%
4-Carboxybenzaldehyde
619-66-9

4-Carboxybenzaldehyde

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 4-formylbenzoate
1571-08-0

methyl 4-formylbenzoate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;97%
levulinic acid
123-76-2

levulinic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

levulinic acid methyl ester
624-45-3

levulinic acid methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;97%
dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

methyl 4-hydroxylbenzoate
99-76-3

methyl 4-hydroxylbenzoate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;97%
2-amino-6-chloro-9<(1'β,4'β)-4'-hydroxycyclopent-2'-enyl>purine
134628-01-6

2-amino-6-chloro-9<(1'β,4'β)-4'-hydroxycyclopent-2'-enyl>purine

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

cis-(+/-)-4-(2-Amino-6-chloro-9H-purin-9-yl)-2-cyclopenten-1-yl methyl carbonate
134628-02-7

cis-(+/-)-4-(2-Amino-6-chloro-9H-purin-9-yl)-2-cyclopenten-1-yl methyl carbonate

Conditions
ConditionsYield
With dmap In dichloromethane Ambient temperature;96%
N-Benzyloxycarbonyl-L-proline
1148-11-4

N-Benzyloxycarbonyl-L-proline

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

N-carbobenzyloxy-L-proline methyl ester
5211-23-4

N-carbobenzyloxy-L-proline methyl ester

Conditions
ConditionsYield
With dmap In tetrahydrofuran for 0.0833333h; Product distribution; Ambient temperature; var. reag., Et3N, var. time and solv.;96%
With dmap In tetrahydrofuran for 0.0833333h; Ambient temperature;96%
3-acetoxybenzoic acid
6304-89-8

3-acetoxybenzoic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

3-acetoxybenzoic acid methyl ester
24781-23-5

3-acetoxybenzoic acid methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 20℃; for 16h;96%
3-Thiophene carboxylic acid
88-13-1

3-Thiophene carboxylic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl thiophene-3-carboxylate
22913-26-4

methyl thiophene-3-carboxylate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;95%
trideuteromethyl ((S)-1-(2-((2S,3S)-3-((S)-2-amino-4-tertbutyldimethylsilyloxy-3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutyl)-2-(4-(pyridin-2-yl)benzyl)hydrazinyl)-3,3-dimethyl-1-oxobutan-2-yl)carbamate
1415634-37-5

trideuteromethyl ((S)-1-(2-((2S,3S)-3-((S)-2-amino-4-tertbutyldimethylsilyloxy-3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutyl)-2-(4-(pyridin-2-yl)benzyl)hydrazinyl)-3,3-dimethyl-1-oxobutan-2-yl)carbamate

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

((5S,8S,9S,14S)-8-benzyl-9-hydroxy-5-(1-tertbutyldimethylsilyloxy-2-methylpropan-2-yl)-15,15-dimethyl-3,6,13-trioxo-11-(4-(pyridin-2-yl)benzyl)-2-oxa-4,7,11,12-tetraazahexadecan-14-yl)carbamic acid trideuteromethyl ester
1415634-38-6

((5S,8S,9S,14S)-8-benzyl-9-hydroxy-5-(1-tertbutyldimethylsilyloxy-2-methylpropan-2-yl)-15,15-dimethyl-3,6,13-trioxo-11-(4-(pyridin-2-yl)benzyl)-2-oxa-4,7,11,12-tetraazahexadecan-14-yl)carbamic acid trideuteromethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; Cooling with ice;95%
2-(1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)pyrimidine-4,5,6- triamine
428854-24-4

2-(1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)pyrimidine-4,5,6- triamine

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-5-pyrimidinyl amino acid methyl ester

4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-5-pyrimidinyl amino acid methyl ester

Conditions
ConditionsYield
In isopropyl alcohol at 20 - 25℃; for 22h; Industry scale;94.8%
In isopropyl alcohol at 20 - 25℃; for 22h; Industry scale;
2-oxoindole
59-48-3

2-oxoindole

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

E-3-(2-ethoxy-2-oxoethylidene)-1-methoxycarbonyl-indoline-2-one

E-3-(2-ethoxy-2-oxoethylidene)-1-methoxycarbonyl-indoline-2-one

Conditions
ConditionsYield
dmap In acetonitrile for 0.25h;94%
p-(acetylamino)benzoic acid
556-08-1

p-(acetylamino)benzoic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 4-acetamidobenzoate
17012-22-5

methyl 4-acetamidobenzoate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;93%
3-Phenylpropionic acid
501-52-0

3-Phenylpropionic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

3-phenylpropanoic acid methyl ester
103-25-3

3-phenylpropanoic acid methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 20℃; for 16h; Product distribution; Further Variations:; Catalysts; Solvents; Temperatures;93%
4-acetyl-benzoic acid
586-89-0

4-acetyl-benzoic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 4-acetylbenzoate
3609-53-8

methyl 4-acetylbenzoate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;93%
dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

Cyclohexanecarboxylic acid
98-89-5

Cyclohexanecarboxylic acid

methyl cyclohexylcarboxylate
4630-82-4

methyl cyclohexylcarboxylate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;93%
(E)-4-[(S)-1-(1H-Indol-3-ylmethyl)-allylamino]-but-3-en-2-one

(E)-4-[(S)-1-(1H-Indol-3-ylmethyl)-allylamino]-but-3-en-2-one

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

3-{(S)-2-[Methoxycarbonyl-((E)-3-oxo-but-1-enyl)-amino]-but-3-enyl}-indole-1-carboxylic acid methyl ester
913337-61-8

3-{(S)-2-[Methoxycarbonyl-((E)-3-oxo-but-1-enyl)-amino]-but-3-enyl}-indole-1-carboxylic acid methyl ester

Conditions
ConditionsYield
With dmap In acetonitrile at 20℃; for 16.6h;93%
(R)-6,8-dimethoxy-1-methyl-3-oxo-1,2,3,4-tetrahydroisoquinoline
1413475-94-1

(R)-6,8-dimethoxy-1-methyl-3-oxo-1,2,3,4-tetrahydroisoquinoline

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

(R)-6,8-dimethoxy-2-(methoxycarbonyl)-1-methyl-3-oxo-1,2,3,4-tetrahydroisoquinoline
1413475-98-5

(R)-6,8-dimethoxy-2-(methoxycarbonyl)-1-methyl-3-oxo-1,2,3,4-tetrahydroisoquinoline

Conditions
ConditionsYield
Stage #1: (R)-6,8-dimethoxy-1-methyl-3-oxo-1,2,3,4-tetrahydroisoquinoline With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.333333h;
Stage #2: dimethyl dicarbonate In tetrahydrofuran at -78℃; for 0.666667h;
93%
nicotinic acid
59-67-6

nicotinic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 3-pyridinecarboxylate
93-60-7

methyl 3-pyridinecarboxylate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;92%
12-hydroxydodecanoic acid
505-95-3

12-hydroxydodecanoic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 12-hydroxydodecanoate
71655-36-2

methyl 12-hydroxydodecanoate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;92%
1,4-dihydropyrano<3,4-b>indol-3-one
6250-86-8

1,4-dihydropyrano<3,4-b>indol-3-one

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 1,4-dihydro-3-oxopyrano<3,4-b>indol-9-carboxylate
146775-03-3

methyl 1,4-dihydro-3-oxopyrano<3,4-b>indol-9-carboxylate

Conditions
ConditionsYield
With dmap In acetonitrile for 0.333333h;91%
adipinic acid monoethyl ester
626-86-8

adipinic acid monoethyl ester

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

adipic acid ethyl methyl ester
18891-13-9

adipic acid ethyl methyl ester

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;91%
3-Cyanobenzoic acid
1877-72-1

3-Cyanobenzoic acid

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

methyl 3-cyanobenzoate

methyl 3-cyanobenzoate

Conditions
ConditionsYield
magnesium(II) perchlorate In nitromethane at 40℃; for 16h;91%

4525-33-1Relevant articles and documents

Howe,Morris

, p. 1901 (1962)

Process For Preparing Dialkyl Dicarbonates

-

Page/Page column 2, (2008/06/13)

The novel process for preparing dialkyl dicarbonates by reacting the corresponding alkyl haloformates with alkali metal hydroxides, alkaline earth metal hydroxides and/or carbonates in the presence of water-immiscible organic solvents and in the presence of a catalyst is characterized in that the catalyst used is at least one tertiary alkylamine of the formula (I) [in-line-formulae]NR1R2R3 ??(I), [/in-line-formulae] where the substituents are each as defined in the description.

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