Name | 4-Dimethylaminobenzhydrazide |
Synonyms | AKOS BC-1518 LABOTEST-BB LT00454413 4-DIMETHYLAMINOBENZHYDRAZIDE 4-Dimethylaminobenzhydrazide 4-Dimethylaminobenzohydrazide 3-(dimethylamino)benzohydrazide 4-(Dimethylamino)-benzoylhydrazine 4-(N,N-DIMETHYLAMINO)BENZHYDRAZIDE 4-DIMETHYLAMINO-BENZOIC ACID HYDRAZIDE 4-(DIMETHYLAMINO)BENZENE-1-CARBOHYDRAZIDE Benzoic acid, 4-(dimethylamino)-, hydrazide |
CAS | 19353-92-5 |
EINECS | 242-985-1 |
InChI | InChI=1/C9H13N3O/c1-12(2)8-5-3-4-7(6-8)9(13)11-10/h3-6H,10H2,1-2H3,(H,11,13) |
InChIKey | UBSSYVLPIDYZJC-UHFFFAOYSA-N |
Molecular Formula | C9H13N3O |
Molar Mass | 179.22 |
Density | 1.156 |
Melting Point | 174-175°C |
BRN | 2210856 |
pKa | 13.12±0.10(Predicted) |
Storage Condition | 2-8℃ |
Refractive Index | 1.601 |
Physical and Chemical Properties | Melting Point 174-175°C BRN 2210856 |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R43 - May cause sensitization by skin contact R40 - Limited evidence of a carcinogenic effect R22 - Harmful if swallowed |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S36/37 - Wear suitable protective clothing and gloves. |
WGK Germany | 3 |
Hazard Class | IRRITANT |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 5.58 ml | 27.899 ml | 55.798 ml |
5 mM | 1.116 ml | 5.58 ml | 11.16 ml |
10 mM | 0.558 ml | 2.79 ml | 5.58 ml |
5 mM | 0.112 ml | 0.558 ml | 1.116 ml |
Use | p-dimethylaminobenzoyl hydrazide is an organic intermediate. |
preparation | p-dimethylaminobenzoyl hydrazide can be prepared from ethyl p-aminobenzoate as raw material, and then obtained by hydrolysis with hydrazine hydrate. There are reports that it can be used to prepare a permanently charged hydrazine sugar marker. A, weigh 1g of ethyl p-aminobenzoate in a two-mouth round bottom flask, add 40ml of acetone to dissolve, then add 3.6g of anhydrous potassium carbonate and 14.1g of methyl iodide, stir and reflux at 80 ℃ under the protection of nitrogen for 24 hours, filter the reaction liquid, take the filtrate, extract with dichloromethane, remove water with magnesium sulfate for the organic phase, evaporate and concentrate after filtering out magnesium sulfate, and separate and purify the product by chromatography column (mobile phase dichloromethane: methanol = 20:1), product A is obtained. B, adding 80% hydrazine hydrate to product a according to a molar ratio of 1:20, 95% ethanol as solvent, refluxing reaction at 90 ℃ under nitrogen protection. after the reaction is completed, chromatography column purification (mobile phase dichloromethane: methanol = 20:1) obtains product B, I .e. p-dimethylaminobenzoyl hydrazide. |