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Malonamide

Malonamide Structure
CAS No.
108-13-4
Chemical Name:
Malonamide
Synonyms
PROPANEDIAMIDE;MALONDIAMIDE;NSC 2134;MALONAMIDE;MALONODIAMIDE;Malonamide>AURORA KA-4099;malonicdiamide;Malonyldiamide;Malonamide 98%
CBNumber:
CB2418973
Molecular Formula:
C3H6N2O2
Molecular Weight:
102.09
MOL File:
108-13-4.mol
MSDS File:
SDS
Modify Date:
2024/3/4 8:47:26

Malonamide Properties

Melting point 172-175 °C (lit.)
Boiling point 191.38°C (rough estimate)
Density 1.3516 (rough estimate)
refractive index 1.5110 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in HCl.
form powder to crystal
pka 7.00±0.70(Predicted)
color White to Almost white
Water Solubility 180 g/L (20 ºC)
BRN 1751401
InChI InChI=1S/C3H6N2O2/c4-2(6)1-3(5)7/h1H2,(H2,4,6)(H2,5,7)
InChIKey WRIRWRKPLXCTFD-UHFFFAOYSA-N
SMILES C(N)(=O)CC(N)=O
CAS DataBase Reference 108-13-4(CAS DataBase Reference)
NIST Chemistry Reference Propanediamide(108-13-4)
EPA Substance Registry System Propanediamide (108-13-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
Safety Statements  22-24/25
WGK Germany  2
RTECS  ON9125000
TSCA  Yes
HS Code  29241900
NFPA 704
0
0 0

Malonamide price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 129593 Malonamide 97% 108-13-4 100G ₹3593.9 2022-06-14 Buy
TCI Chemicals (India) M0027 Malonamide 108-13-4 25G ₹2200 2022-05-26 Buy
ALFA India ALF-A17939-36 Malonamide, 98% 108-13-4 500g ₹14356 2022-05-26 Buy
ALFA India ALF-A17939-22 Malonamide, 98% 108-13-4 100g ₹3477 2022-05-26 Buy
TCI Chemicals (India) M0027 Malonamide 108-13-4 500G ₹11800 2022-05-26 Buy
Product number Packaging Price Buy
129593 100G ₹3593.9 Buy
M0027 25G ₹2200 Buy
ALF-A17939-36 500g ₹14356 Buy
ALF-A17939-22 100g ₹3477 Buy
M0027 500G ₹11800 Buy

Malonamide Chemical Properties,Uses,Production

Description

Malonamide is a dicarboxylic acid diamide that is malonic acid in which both carboxy groups have been replaced by carbamoyl groups. It is functionally related to a malonic acid.

Chemical Properties

White crystalline powder

Uses

The malonamide-based ionic liquid extractant was used in the extraction of europium(iii) and other trivalent rare-earth ions from nitric acid medium.

Uses

Malonamide is used in the synthesis of malonamic acid, malonamate and malonamide derivative of some heterocyclic compounds with antiinflammatory activity.

General Description

The malonamide derivatives are obtained by the one-pot, five-component condensation reaction of isocyanide, Meldrum′s acid, arylidene malononitrile, and two amine molecules in CH2Cl2.

Hazard

Mildly toxic by ingestion.

Synthesis

The synthesis of Malonamide is as follows:
A typical reaction was carried out in a 10 mL flask. Benzonitrile (2 mmol), CuII-4 ? (0.2 g), acetaldoxime (6 mmol) and MeOH (4 mL) were stirred at 65 °C for 4 h. The solid was filtered, washed with MeOH and the filtrate evaporated. The residue was subjected to GC-MS analysis and NMR spectroscopy. The filtered catalyst can be recycled after drying at about 150 °C for 1 h.
synthesis of Malonamide.png

Purification Methods

Crystallise the amide from water. [Beilstein 2 IV 1887.]

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MALONODIAMIDE MALONIC ACID DIAMIDE MALONIC ACID AMIDE MALONAMIDE METHANEDICARBOXYLIC ACID DIAMIDE DICARBOXYMETHANE DIAMIDE LABOTEST-BB LT01598526 AURORA KA-4099 CARBOXAMIDOACETAMIDE CARBOXYACETIC ACID DIAMIDE PROPANEDIOIC ACID DIAMIDE malonicdiamide Malonyldiamide MALONAMIDE, FOR FLUORESCENCE MALONAMIDE 99+% Malonamide 98% Propane-1,3-diamide MALONAMIDE extrapure 3-Amino-3-oxopropanamide Malonamide,97% NSC 2134 Propylene aMide MALONAMIDE FOR SYNTHESIS 100 G MalonaMide , 98.0%(N) Malonamide> Malonamide ISO 9001:2015 REACH MALONDIAMIDE PROPANEDIAMIDE 108-13-4 CH2CONH22 C3H6NO2 Organic Building Blocks Fluorescent Probes, Labels, Particles and Stains Detection Building Blocks Biochemicals and Reagents BioChemical Amides Carbonyl Compounds Aliphatics Miscellaneous Reagents Amides Biochemicals and Reagents Building Blocks C2 to C7 Carbonyl Compounds Chemical Synthesis Derivatization agents Luminescent Compounds/Detection Organic Building Blocks Wavelength Index API intermediates