N,N′-Dimethylethylenediamine
ALDRICH/D157805 - 98%
Synonym: DMEDA; 1,2-
CAS Number: 110-70-3
Empirical Formula (Hill Notation): C4H12N2
Molecular Weight: 88.15
EC Number: 203-793-3
MDL Number: MFCD00008290
Linear Formula: CH3NHCH2CH2NHCH3
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D157805-100G.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D157805-500G.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D157805-5G.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D157805-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D157805-5G
| assay | 98% |
| bp | 119 °C (lit.) |
| density | 0.819 g/mL at 20 °C (lit.) |
| form | liquid |
| InChI | 1S/C4H12N2/c1-5-3-4-6-2/h |
| InChI key | KVKFRMCSXWQSNT-UHFFFAOYSA |
| Quality Level | 200  |
| refractive index | n |
| SMILES string | CNCCNC |
| Application: | N,N′-Dimethylethylenediamine can be used as a ligand in the following processes: • Copper-catalyzed cyanations of aryl bromides using potassium hexacyanoferrate(II) to form the corresponding benzonitriles. • Copper-catalyzed tandem reaction of carbodiimide and isocyanoacetate to form benzoimidazo[1,5-α]imidaz • Aminothiolation of 1,1-dibromoalkene to form N-fused heterocycles. • In combination with ferrous chloride, for the N-arylation of NH-sulfoximines with aryl iodides to form N-arylsulfoximines. • It can catalyze the direct C-H arylation of unactivated benzene in the presence of potassium tert-butoxide to form the corresponding biaryl. |
| Packaging: | 5, 25, 100, 500 g in glass bottle |
| Symbol |   GHS02,GHS05 |
| Signal word | Danger |
| Hazard statements | H226 - H314 |
| Precautionary statements | P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338 |
| Hazard Codes | C |
| Risk Statements | 10-34 |
| Safety Statements | 26-36/37/39-45 |
| RIDADR | UN 2734PSN2 3(8) / PGII |
| WGK Germany | WGK 3 |
| Flash Point(F) | 78.8 °F - closed cup |
| Flash Point(C) | 26 °C - closed cup |
| Purity | 98% |
| bp | 119 °C (lit.) |
| Density | 0.819 g/mL at 20 °C (lit.) |
| Refractive Index | n |
| UNSPSC | 12352100 |