- Product Name:
- BENZAMIDE, SUBLIMED, ZONE-REFINED, 99.9%
- Product Categories:
- Bioactive Small Molecules
- Building Blocks
- Carbonyl Compounds
- Cell Biology
- Chemical Synthesis
- Organic Building Blocks
- PARP (Poly(ADP-Ribose) polymerase)
- PARP Inhibitors
- Apoptosis and Cell Cycle
- C2 to C7
- Cell Signaling and Neuroscience
- Highly Purified Reagents
- Other Categories
- Zone Refined Products
- Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
- Pharmaceutical Intermediates
- Mol File:
Benzamide Chemical Properties
- Melting point:
- 125-128 °C(lit.)
- Boiling point:
- vapor pressure
- 0.000056 hPa (20 °C)
- refractive index
- 1.5323 (estimate)
- Flash point:
- storage temp.
- Store below +30°C.
- ethanol: soluble50mg/mL, clear to very slightly hazy, colorless to light yellow
- 13.0(at 25℃)
- Crystalline Powder
- White to almost white
- 6.9 (H2O)(saturated solution)
- PH Range
- Water Solubility
- 1.35 g/100 mL (20 ºC)
- Stable. Combustible. Incompatible with strong oxidizing agents.
- CAS DataBase Reference
- 55-21-0(CAS DataBase Reference)
- NIST Chemistry Reference
- EPA Substance Registry System
- Benzamide (55-21-0)
Benzamide Usage And Synthesis
Benzamide appears as off-white crystals or powder. It is combustible and incompatible with strong oxidising agents and strong bases. On combustion and thermal decomposition, it emits nitrogen oxides, carbon monoxide, and carbon dioxide.
Benzamide is a carbonic acid amide of benzoic acid. Benzamide exhibits an angle of about 15º with the plane of the amide group; this shows that benzamide molecule is not flat. The rotation of the amide group relative to the aromatic ring may result from the repulsion interaction between the hydrogen atoms of the amide group and those of the aromatic ring.
Benzamide is a combustible, colorless to beige, off-white, crystalline solid; freezing/melting point=132-133° C. It is slightly soluble in water, and soluble in many organic solvents.
Benzamide was used to study the mechanism of photocatalytic decomposition of aqueous solution of acetic acid, acetamide and acetonitrile in the presence of semiconductors. It was used to develop a robust screening method to study biotransformations using (+)-γ-lactamase enzyme.
Take a mixture of 5 ml concentrated ammonia and 5 ml water in a conical flask with a well-fitting cork. Add 2 ml (2.4 g.) benzoyl chloride, cork the flask and shake vigorously. Heat generates due to the reaction, hence hold the cork securely during shaking. After 15 min not even a trace of oily benzoyl chloride remains. Filter the fine flakes, wash with cold water and recrystallise from hot water: yield, 1-5 g. Colourless crystals of benzamide.
Preparation of benzamide from benzoyl chloride
ChEBI: An aromatic amide that consists of benzene bearing a single carboxamido substituent. The parent of the class of benzamides.
The Journal of Organic Chemistry, 59, p. 4114, 1994 DOI: 10.1021/jo00094a021
Chemical and Pharmaceutical Bulletin, 39, p. 1152, 1991 DOI: 10.1248/cpb.39.1152
Synthetic Communications, 20, p. 1445, 1990 DOI: 10.1080/00397919008052860
Air & Water Reactions
Insoluble in water.
Benzamide reacts with azo and diazo compounds to generate toxic gases. Forms flammable gases with strong reducing agents. Mixing with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. Combustion generates toxic mixed oxides of nitrogen (NOx).
Depresses the central nervous system; toxic.
Flash point data for Benzamide are not available, however Benzamide is probably combustible.
Benzamide on radioiodination by different labeling procedures results in large-scale production of radioiodinated benzamides having potential therapeutic application for patients with metastatic malignant melanoma.
Benzamide is used in organic synthesis.
Crystallise it from hot water (about 5mL/g), EtOH or 1,2-dichloroethane, and dry it in air. It has also been crystallised from dilute aqueous NH3, H2O, Me2CO, then *C6H6 using a Soxhlet extractor. Dry it in an oven at 110o for 8hours and store in a desiccator over 99% H2SO4. [Bates & Hobbs J Am Chem Soc 73 2151 1951, Beilstein 9 IV 725.]
Benzamide Preparation Products And Raw materials
- 010-82848833- ;010-82848833-
- 400-610-6006; 021-67582000
- 4-[(2,4-Dimethoxyphenyl)(Fmoc-amino)methyl]phenoxyacetic acid
- Ethyl 2-(Chlorosulfonyl)acetate
- Ascoric Acid