Nome do produto:
Diethylmalonat
Descrição:
Diethylmalonat s present in guava fruit, melon, concord grape, pineapple, blackberry and many wines and spirits Malonic acid,it e is found in alcoholic beverages and mainly used as flavour ingredient. Its molecular formula is C7H12O4.
Grupo:
Solvents
Número CAS:
105-53-3
Número EC:
203-305-9
Sinônimos:
diethyl propanedioate, Propanedioic acid, diethyl ester, Diethyl Malonate, Ethyl Malonate, Malonic acid diethyl ester, Diethyl malonate, Malonic acid diethyl ester, Diethylmalonat, Malonsäurediethylester, Diethyl malonate
Anexos:
Consumer use, Personal Care, Paint, Adhesive, Automotive Care, Building Material
Nome IUPAC:
diethyl propanedioate
Fórmula molecular:
C7H12O4
Peso molecular:
160.169 g/mol
Ponto de ebulição:
199ºC
Ponto de inflamação:
90ºC
Ponto de fusão:
-50ºC
Solubilidade:
Solubility in water, g/l at 20 °C: 20
Densidade:
1.055 g/cm3
Código HS:
2917190090
RID/ADR:
2917190090
Declarações de risco:
R36/37/38
Declaração de Perigo:
Pharmaceutical Intermediates
Declaração de Cuidado:
R36/37/38
Fornecedores: 34
Wego Chemical Group
Netherlands
Diethylmalonat
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Univar Solutions GmbH
Germany
Diethylmalonat
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Traditem GmbH
Germany
Diethylmalonat
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Diethyl malonate
Product Name: Diethyl malonate
Synonyms: Diethyi malonate;Malonic Acid Diethyl Ester Ethyl Malonate;Diethyl malonate,Malonic acid diethyl ester;Diethyl Malonate, 99+% 25GR;Diethyl Malonate, 99+% 500GR;MALONIC ACID DIETHYL ESTER;MALONIC ESTER;ETHYL MALONATE
CAS: 105-53-3
MF: C7H12O4
MW: 160.17
EINECS: 203-305-9
Product Categories: Building Blocks;C6 to C7;Organics;Carbonyl Compounds;Chemical Synthesis;Esters;Organic Building Blocks
Mol File: 105-53-3.mol
Diethylmalonat
Pharmaceutics
99%
TT Advance
CIF
SUZHOU, CHINA
Aplicação:
Diethyl malonate is the diethyl ester of malonic acid. It naturally occuring in grapes and strawberries, is widely used in the manufacture of pharmaceuticals, antioxidants, and dyes. Diethyl malonate is used in organic synthesis for the preparation of alpha-aryl malonates, mono-substituted and di-substituted acetic acid, barbiturates and artificial flavorings. It is also involved in the synthesis of pharmaceuticals like chloroquine, butazolidin and barbital. It acts as intermediate in the synthesis of vitamin B1, vitamin B6, non-steroidal anti-inflammatory agents agrochemicals and perfumes. In Knoevenagel condensation reaction, it reacts with benzaldehyde to get diethyl benzylidenemalonate.
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SYSKEM
Germany
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STOCKMEIER HOLDING GMBH
Spain
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Radchem Products, Inc.
United States
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RT VANDERBILT HOLDING CO INC
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OQEMA
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Nanjing Lanya Chemical
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Möller Chemie GmbH & Co. KG
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Matrix Fine Chemicals GmbH
Switzerland
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Julius Hoesch GmbH & Co. KG
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Ireland
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INTEGRATED TRAFFIC SYSTEMS INC
United States
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Häffner GmbH & Co. KG
Germany
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HighChem Company LTD.
Japan
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Donauchem GmbH
Austria
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Chenseg Europe
Germany
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Chemicals United B.V.
Netherlands
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CEDACHEM
Germany
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200
kg
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Brenntag Polska
Poland
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Brenntag GmbH
Germany
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India
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BCD Chemie GmbH
Germany
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Apollo Scientific LTD
United Kingdom
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ALL Chemistry Inc.
United States
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