Product Name

  • Name

    DIMETHYL DICARBONATE

  • EINECS 224-859-8
  • CAS No. 4525-33-1
  • Density 1.243 g/cm3
  • Solubility
  • Melting Point 15-17oC
  • Formula C4H6O5
  • Boiling Point 171.4 °C at 760 mmHg
  • Molecular Weight 134.089
  • Flash Point 80 °C
  • Transport Information UN 2927 6.1/PG 2
  • Appearance
  • Safety 18-26-28-36/37/39-38-45
  • Risk Codes 21/22-23-34
  • Molecular Structure Molecular Structure of 4525-33-1 (DIMETHYL DICARBONATE)
  • Hazard Symbols ToxicT
  • Synonyms Dicarbonicacid, dimethyl ester (9CI);Formic acid, oxydi-, dimethyl ester (7CI,8CI);Dimethyl pyrocarbonate;Methyl pyrocarbonate;Pyrocarbonic acid dimethyl ester;Velcorin;
  • PSA 61.83000
  • LogP 0.53580

Synthetic 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%

Dimethyl dicarbonate Specification

The CAS registry number of Dimethyl dicarbonate is 4525-33-1. Its EINECS registry number is 224-859-8. The IUPAC name is methoxycarbonyl methyl carbonate. In addition, the molecular formula is C4H6O5 and the molecular weight is 134.09. It is also called Dicarbonic acid,C,C'-dimethyl ester. What's more, it is a colourless liquid with a sharp odour. What's more, it should be stored in sealed container, and placed in a cool, ventilated and dry place.

Physical properties about this chemical are: (1)ACD/LogP: 0.42; (2)ACD/LogD (pH 5.5): 0.42; (3)ACD/LogD (pH 7.4): 0.42; (4)ACD/BCF (pH 5.5): 1.23; (5)ACD/BCF (pH 7.4): 1.23; (6)ACD/KOC (pH 5.5): 40.33; (7)ACD/KOC (pH 7.4): 40.33; (8)#H bond acceptors: 5; (9)#Freely Rotating Bonds: 4; (10)Polar Surface Area: 61.83 Å2; (11)Index of Refraction: 1.395; (12)Molar Refractivity: 25.87 cm3; (13)Molar Volume: 107.8 cm3; (14)Polarizability: 10.25 ×10-24cm3; (15)Surface Tension: 33.9 dyne/cm; (16)Density: 1.242 g/cm3; (17)Flash Point: 80 °C; (18)Enthalpy of Vaporization: 40.78 kJ/mol; (19)Boiling Point: 171.4 °C at 760 mmHg; (20)Vapour Pressure: 1.4 mmHg at 25 °C.

Uses of Dimethyl dicarbonate: it is used as a beverage preservative or processing aid or sterilant. And it can be used as a preservative in wine as a replacement to sulfur dioxide, inactivating wine spoilage yeasts such as Brettanomyces. Moreover, it can be used to stabilise non alcoholic beverages such as carbonated or non carbonated juice beverages, isotonic sports beverages, iced teas and flavoured waters. In addition, it can react with furan-2-carboxylic acid to get furan-2-carboxylic acid methyl ester. This reaction will need reagent 4-dimethylaminopyridine and solvent tetrahydrofuran. The reaction time is 88 hours. The yield is about 97%.

Dimethyl dicarbonate can react with furan-2-carboxylic acid to get furan-2-carboxylic acid methyl ester

When you are using this chemical, please be cautious about it as the following:
This chemical is harmful by inhalation and in contact with skin. And it can cause burns. You should handle and open container with care. During using it, wear suitable protective clothing, gloves and eye/face protection. In case of insufficient ventilation, wear suitable respiratory equipment. What's more, in case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If it contact with your skin, wash it immediately with plenty of ... (to be specified by the manufacturer). In addition, in case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.).

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(OC)OC(=O)OC
(2)InChI: InChI=1/C4H6O5/c1-7-3(5)9-4(6)8-2/h1-2H3
(3)InChIKey: GZDFHIJNHHMENY-UHFFFAOYAQ

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 oral 589mg/kg (589mg/kg)   Weisheng Dulixue Zazhi. Journal of Health Toxicology. Vol. 6, Pg. 104, 1992.
rat LC50 inhalation 711mg/m3/4H (711mg/m3) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: TREMOR

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
National Technical Information Service. Vol. OTS0545284,
rat LD50 oral 260mg/kg (260mg/kg)   Weisheng Dulixue Zazhi. Journal of Health Toxicology. Vol. 6, Pg. 104, 1992.

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