156272
3,5-Dinitrobenzoyl chloride
≥96.5%, solid
Synonym(s):
DNBC, NSC 2697
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(O2N)2C6H3COCl
CAS Number:
Molecular Weight:
230.56
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-750-6
MDL number:
Beilstein/REAXYS Number:
990249
Assay:
≥96.5%
Form:
solid
Product Name
3,5-Dinitrobenzoyl chloride, ≥96.5%
vapor density
7.6 (vs air)
Quality Level
assay
≥96.5%
form
solid
bp
196 °C/11 mmHg (lit.)
mp
68-69 °C (lit.)
functional group
acyl chloride, nitro
SMILES string
[O-][N+](=O)c1cc(cc(c1)[N+]([O-])=O)C(Cl)=O
InChI
1S/C7H3ClN2O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H
InChI key
NNOHXABAQAGKRZ-UHFFFAOYSA-N
General description
Crystals of 3,5-dinitrobenzoyl chloride (DNBC) belong to the orthorhombic crystal system and space group Pna21. It is widely used reagent for the detection of alcohols.
Application
3,5-Dinitrobenzoyl chloride may be used for the quantitative estimation of hydroxyl groups in pyridine. It may be used in the synthesis of following:
3,5-Dinitrobenzoyl chloride may also be used as derivatizing agent for the following:
- 3,5-diamino-N-cyclopropylbenzamide
- 3,5-dinitro-N-cyclopropylbenzamide
- 4-(3,5-dinitrophenyl)-6-(dipropan-2-ylamino)-2H-1,3,5-thiadiazine-2-thione4
3,5-Dinitrobenzoyl chloride may also be used as derivatizing agent for the following:
- biogenic amines present in fermented foods, which can be determined using liquid chromatography method(LC)
- polyamines, present in biological fluids, which can be determined using high performance liquid chromatography(HPLC)
Still not finding the right product?
Explore all of our products under 3,5-Dinitrobenzoyl chloride
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and characterization of aromatic poly (amides) based on 3, 5-diamino-N-cyclopropylbenzamide.
Tundidor-Camba A, et al.
Royal Society of Chemistry Advances, 5(29), 23057-23066 (2015)
Rapid Determination of Organic Hydroxyl Groups with 3, 5,-Dinitrobenzoyl Chloride.
Robinson Jr WT, et al.
Analytical Chemistry, 33(8), 1030-1034 (1961)
A Markowska et al.
Roczniki Akademii Medycznej w Bialymstoku (1995), 42(1), 129-140 (1997-01-01)
A carbocyclic analogue of distamycin was obtained, in which the N-methylpyrrole rings were substituted by disubstituted benzene rings. Additionally, N-chloro- or N-bromoacetyl groups, displaying alkylating properties, were introduced. The synthesis, starting from 3,5-dinitrobenzoyl chloride, consisted of five stages.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 156272-25G | 04061838742605 |
| 156272-100G | 04061838742599 |