3,5-Dinitrobenzamide
3,5-Dinitrobenzamide (CAS 121-81-3) is an organic compound with the molecular formula C7H5N3O5 and a molecular weight of 211.13 g/mol. This nitromide derivative functions as a key building block in organic synthesis and chemical research. Its primary applications are in the development of novel compounds and as an intermediate in the production of more complex molecules. Tech Serve Solutions supplies this chemical for laboratory and industrial research purposes.
- IUPAC
- Nitromide
- Synonyms
- (O2N)2C6H3CONH2
Organic Synthesis Intermediate
3,5-Dinitrobenzamide serves as a valuable intermediate in the synthesis of various organic compounds. Its reactive functional groups allow for diverse chemical transformations.
Chemical Research Building Block
This compound is utilised as a building block in academic and industrial research laboratories for the construction of novel molecular structures and the exploration of new chemical pathways.
Development of Specialty Chemicals
It finds application in the development of specialty chemicals, where its unique structure can be incorporated into target molecules with specific properties.
| Molecular weight | 211.13 |
|---|---|
| Linear formula | (O2N)2C6H3CONH2 |
| Assay | 97% |
| Melting point | 183-185 °C(lit.) |
Hazard statements
- H302Harmful if swallowed
| Protective equipment | dust mask type N95 (US), Eyeshields, Gloves |
|---|---|
| Water hazard class (WGK, DE) | 3 |
| Hazard codes (EU) | Xn |
| Risk statements (R) | 22 |
| Safety statements (S) | 26-36 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is 3,5-Dinitrobenzamide primarily used for?
+
3,5-Dinitrobenzamide is primarily used as an intermediate in organic synthesis and as a building block in chemical research for creating novel compounds.
What is the CAS number and formula for 3,5-Dinitrobenzamide?
+
The CAS number for 3,5-Dinitrobenzamide is 121-81-3, and its linear formula is (O2N)2C6H3CONH2.
What grade and purity does Tech Serve Solutions supply for 3,5-Dinitrobenzamide?
+
Tech Serve Solutions supplies 3,5-Dinitrobenzamide with an assay of 97%. We do not represent this product as USP, BP, or EP grade.
How should 3,5-Dinitrobenzamide be handled safely?
+
3,5-Dinitrobenzamide is classified with the hazard statement H302 (Harmful if swallowed). It requires handling with appropriate personal protective equipment, including a dust mask (type N95 US), eyeshields, and gloves, in a well-ventilated area.
Does Tech Serve Solutions export 3,5-Dinitrobenzamide?
+
Yes, Tech Serve Solutions is a specialist global supplier and exporter of fine chemicals, including 3,5-Dinitrobenzamide.
How can I request a quote or sample for 3,5-Dinitrobenzamide?
+
To request a quote or a sample for 3,5-Dinitrobenzamide, please contact our sales team through the website or by phone.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis