564613
5-Amino-2-nitrobenzoic acid
97%
Synonym(s):
2-Nitro-5-aminobenzoic acid, 3-Carboxy-4-nitroaniline, NSC 74455
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About This Item
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Quality Level
Assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
236-238 °C (lit.)
application(s)
peptide synthesis
SMILES string
Nc1ccc(c(c1)C(O)=O)[N+]([O-])=O
InChI
1S/C7H6N2O4/c8-4-1-2-6(9(12)13)5(3-4)7(10)11/h1-3H,8H2,(H,10,11)
InChI key
KZZWQCKYLNIOBT-UHFFFAOYSA-N
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Related Categories
Application
Reactant for:
- Two-component dendritic chain reactions
- Enzymic activation of hydrophobic self-immolative dendrimers
- Preparation of insulin receptor tyrosine kinase activator
- Preparation of polymer-bound diazonium salts using Merrifield resin-bound piperazine
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Ox. Sol. 2
Storage Class Code
5.1B - Oxidizing hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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5-amino-2-nitrobenzoic acid as a reference material for the determination of gamma-GT activity.
Clinica chimica acta; international journal of clinical chemistry, 160(1), 63-67 (1986-10-15)
Biosensors & bioelectronics, 24(4), 982-986 (2008-09-09)
Herein, we reported for the first time one step procedure for the preparation of cytochrome c (cyt c)-poly (5-amino-2-napthalenesulfonic acid) (PANS) modified glassy carbon electrode by cyclic voltammetrically (CV). Hereafter, we called the above modified electrode as cyt c-PANS electrode.
Clinical chemistry, 33(11), 1978-1982 (1987-11-01)
We describe the process of certification for a gamma-glutamyltransferase reference material (CRM no. 319). Fifteen laboratories participated to this interlaboratory evaluation. All steps of the measurements were controlled in an effort to locate potential sources of variations. In particular, the
Chemical communications (Cambridge, England), 46(35), 6575-6577 (2010-08-18)
A new dendritic chain reaction probe system was demonstrated to produce exponential signal amplification for the detection of sulfhydryl compounds.
Biochemical and biophysical research communications, 319(1), 185-188 (2004-05-26)
A tetrapeptide combinatorial library, considered as chromogenic substrates of bovine beta-trypsin, was synthesized by the solid phase method. The peptides contain an analog of p-nitroanilide, obtained by attaching 5-amino-2-nitrobenzoic acid (Anb(5,2)) to the C-termini. Deconvolution of the peptide library, performed
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