3,5-Dinitrobenzoyl chloride, 98+%
3,5-Dinitrobenzoyl chloride, 98+%
3,5-Dinitrobenzoyl chloride, 98+%
3,5-Dinitrobenzoyl chloride, 98+%
Thermo Scientific Chemicals

3,5-Dinitrobenzoyl chloride, 98+%

CAS: 99-33-2 | C7H3ClN2O5 | 230.56 g/mol
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25 g
100 g
Catalog number A16729.14
also known as A16729-14
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Quantity:
25 g
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Price (USD)
42.65
Online Exclusive
47.30
Save 4.65 (10%)
Each
Add to cart
Chemical Identifiers
CAS99-33-2
IUPAC Name3,5-dinitrobenzoyl chloride
Molecular FormulaC7H3ClN2O5
InChI KeyNNOHXABAQAGKRZ-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC(=CC(=C1)C(Cl)=O)[N+]([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or needles or powder or crystalline powder
Appearance (Color)White to cream to yellow to brown
Assay (Titration ex Chloride)≥98.0 to ≤102.0%
Melting Point67-72?C, may be slight turbidity
Identification (FTIR)Conforms
Used in photography. This aromatic compound is used by chemists to identify alcohol components in esters and in the fluorometric analysis of creatinine.

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
Used in photography. This aromatic compound is used by chemists to identify alcohol components in esters and in the fluorometric analysis of creatinine.

Solubility
Slightly soluble in water.

Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, bases, water.
RUO – Research Use Only

General References:

  1. A Markowska et. al. Synthetic analogues of netropsin and distamycin. IV. Synthesis of a new carbocyclic analogue of distamycin with alkylating side groups.. Journal name. year of publication , 42 (1),129-140 .
  2. S Wongyai et. al. HPLC analysis of polyamines and their acetylated derivatives in the picomole range using benzoyl chloride and 3,5-dinitrobenzoyl chloride as derivatizing agent.. Biomedical Chromatography. 1988, 2(6),254-257.
  3. Reagent for preparation of crystalline derivatives of alcohols: J. Org. Chem., 51, 4819, 4991 (1986); 52, 2086 (1987). Also used for characterization and separation of amines as their sulfonamides: J. Org. Chem., 49, 3043 (1984); 51, 4991 (1986); J. Am. Chem. Soc., 108, 6054 (1986).