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Malononitrile, 99%, Thermo Scientific Chemicals

29.75 EUR - 549.74 EUR

Chemical Identifiers

CAS 109-77-3
Molecular Formula C3H2N2
MDL Number MFCD00001883
InChI Key CUONGYYJJVDODC-UHFFFAOYSA-N
Synonym malononitrile, dicyanomethane, cyanoacetonitrile, malonic dinitrile, methylene cyanide, dicyanmethane, malonodinitrile, malonic acid dinitrile, methylenedinitrile, methane, dicyano
PubChem CID 8010
ChEBI CHEBI:33186
IUPAC Name propanedinitrile
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Products 4
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Product Code Brand Quantity Price Quantity & Availability  
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Thermo Scientific Alfa Aesar
A15046.06
5 g
29.75 EUR
5g
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11467307
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Thermo Scientific Alfa Aesar
A15046.22
100 g
31.96 EUR
100g
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Thermo Scientific Alfa Aesar
A15046.36
500 g
102.51 EUR
500g
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Thermo Scientific Alfa Aesar
A15046.0E
2500 g
549.74 EUR
2500g
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Description

Description

Crosslinking agent for modification of proteins via amidationMalononitrile is used as a precursor in the preparation of anti-cancer drug, triamterene, adenine, methotrexate, thiamine, acrylic fibers and dyes. It is used in Knoevenagel condensation to prepare 2-chlorobenzalmalononitrile by reacting with 2-chlorobenzaldehyde. It acts as a leaching agent for gold. It is used as a raw material for the Gewald reaction of ketone or aldehyde to produce 2-aminothiophene using elemental sulfur and a base. Further, it plays an important role in the preparation of [1,6]-naphthyridines, gamma-ketoamides, 1,4-dihydropyridine, chromeno[2,3-b]pyridine and dihydro-1,4-dithiepine frameworks.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Crosslinking agent for modification of proteins via amidationMalononitrile is used as a precursor in the preparation of anti-cancer drug, triamterene, adenine, methotrexate, thiamine, acrylic fibers and dyes. It is used in Knoevenagel condensation to prepare 2-chlorobenzalmalononitrile by reacting with 2-chlorobenzaldehyde. It acts as a leaching agent for gold. It is used as a raw material for the Gewald reaction of ketone or aldehyde to produce 2-aminothiophene using elemental sulfur and a base. Further, it plays an important role in the preparation of [1,6]-naphthyridines, gamma-ketoamides, 1,4-dihydropyridine, chromeno[2,3-b]pyridine and dihydro-1,4-dithiepine frameworks.

Solubility
Soluble in water, acetone, acetic acid, chloroform, ethanol, ether and benzene.

Notes
Store in a cool place. Incompatible with strong oxidizing agents, strong reducing agents, strong acids and strong bases.
Specifications

Chemical Identifiers

109-77-3
MFCD00001883
malononitrile, dicyanomethane, cyanoacetonitrile, malonic dinitrile, methylene cyanide, dicyanmethane, malonodinitrile, malonic acid dinitrile, methylenedinitrile, methane, dicyano
CHEBI:33186
C3H2N2
CUONGYYJJVDODC-UHFFFAOYSA-N
8010
propanedinitrile

Specifications

109-77-3
1.049
112°C
1.415
UN2647
14,5711
Soluble aq. soln.,acetone,acetic acid,chloroform,ethanol,ether and benzene.
N#CCC#N
66.06
CHEBI:33186
99%
30°C to 34°C
220°C to 222°C
C3H2N2
MFCD00001883
773697
malononitrile, dicyanomethane, cyanoacetonitrile, malonic dinitrile, methylene cyanide, dicyanmethane, malonodinitrile, malonic acid dinitrile, methylenedinitrile, methane, dicyano
CUONGYYJJVDODC-UHFFFAOYSA-N
propanedinitrile
8010
66.06
Malononitrile
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Safety and Handling

Safety and Handling

GHS H Statement

H301-H311-H331

Toxic if swallowed.

Toxic in contact with skin.

Toxic if inhaled.

P261-P264b-P270-P271-P280-P301+P310-P302+P352-P304+P340-P311-P312-P330-P361-P363-P501c

H301+H311+H331

missing translation for 'dotInformation' : Transport Hazard Class: 6.1; Packing Group: II; Proper Shipping Name: MALONONITRILE

missing translation for 'einecsNumber' : 203-703-2

missing translation for 'rtecsNumber' : OO3150000

missing translation for 'tsca' : Yes

Recommended Storage : Ambient temperatures

SDS
Documents

Documents

Product Certifications

RUO – Research Use Only