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Key Documents

Safety Information

524417

Sigma-Aldrich

3,5-Dinitro-o-toluamide

98%

Synonym(s):

2-Methyl-3,5-dinitrobenzamide

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100 μG
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100 μG
CN¥4,472.02

About This Item

Linear Formula:
(O2N)2C6H2(CH3)CONH2
CAS Number:
Molecular Weight:
225.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

CN¥4,472.02


Available to ship onApril 14, 2025Details


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Assay

98%

mp

170-180 °C (lit.)

functional group

amide
nitro

SMILES string

Cc1c(cc(cc1[N+]([O-])=O)[N+]([O-])=O)C(N)=O

InChI

1S/C8H7N3O5/c1-4-6(8(9)12)2-5(10(13)14)3-7(4)11(15)16/h2-3H,1H3,(H2,9,12)

InChI key

ZEFNOZRLAWVAQF-UHFFFAOYSA-N

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1 of 4

This Item
OGS107OGS106OGS507
peptide cleavage

no cleavage

peptide cleavage

no cleavage

peptide cleavage

no cleavage

peptide cleavage

no cleavage

origin of replication

pUC (500 copies)

origin of replication

pUC (500 copies)

origin of replication

pUC (500 copies)

origin of replication

pUC (500 copies)

bacteria selection

ampicillin

bacteria selection

ampicillin

bacteria selection

ampicillin

bacteria selection

kanamycin

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution

mol wt

size 2686 bp

mol wt

size 4310 bp

mol wt

size 4309 bp

mol wt

size 7694 bp

General description

Water solubility of 3,5-Dinitro-o-toluamide (3,5-DNoTAME) is 447.5mg/L. It affords 3-amino-5-nitro-o-toluamide, via biological reduction.[1] 3,5-DNoTAME also forms colored complexes on reaction with various diamines and organic solvents.[2]

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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S J Ball et al.
Parasitology research, 73(4), 293-297 (1987-01-01)
Medication of chicks with 125 ppm amprolium or dinitolmide adversely affected oocyst sporulation of Eimeria acervulina (Weybridge strain). Dinitolmide delayed oocyst production and no oocyst wall formation was seen up to 168 h post infection. Both drugs caused large numbers
T Ohta et al.
Mutation research, 77(1), 21-30 (1980-01-01)
18 feed additives were tested for DNA-modifying effects by the repair test named "rec-assay" with Bacillus subtillis H17 (rec+) and M45 (rec-), and for mutagenicity with Escherichia coli WP2 hcr and 5 Salmonella typhimurium tester strains with the use of
Anticoccidial drugs: effects on infectivity and survival intracellularly of Eimeria tenella sporozoites.
L R McDougald et al.
Experimental parasitology, 40(3), 314-319 (1976-12-01)
Feed Additive Residues, Isolation and Identification of Amino-nitro-o-toluamide Formed by Biological Reduction of 3, 5-Dinitro-o-tuamide.
Smith GN, et al.
Journal of Agricultural and Food Chemistry, 11(3), 257-260 (1963)
L P Joyner et al.
Parasitology, 75(2), 155-164 (1977-10-01)
Chicks infected with the Weybridge strains of Eimeria maxima and E. acervulina were not protected by the normal levels of amprolium, but the sporulation of the oocysts was inhibited. With higher drug concentrations, fewer oocysts were produced. E brunetti was

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