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Merck

D12805

Sigma-Aldrich

3,5-Diaminobenzoic acid

98%, for peptide synthesis

Sinónimos:

3,5-DABA, 5-Carboxy-1,3-phenylenediamine, DABA

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About This Item

Fórmula lineal:
(H2N)2C6H3CO2H
Número de CAS:
Peso molecular:
152.15
Beilstein/REAXYS Number:
2086484
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

product name

3,5-Diaminobenzoic acid, 98%

Quality Level

assay

98%

form

powder with small lumps

reaction suitability

reaction type: solution phase peptide synthesis

mp

235-238 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cc(N)cc(c1)C(O)=O

InChI

1S/C7H8N2O2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3H,8-9H2,(H,10,11)

Inchi Key

UENRXLSRMCSUSN-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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J Beckmann et al.
Acta diabetologica latina, 18(1), 51-57 (1981-01-01)
DNA content seems to be an ideal reference parameter for data on secretory function or metabolism of pancreatic islets. The approved fluorometric DNA assay with diaminobenzoic acid (DABA) of Kissane and Robins comprises repeated ethanol extractions of the tissue for
C F Kuo et al.
Analytical biochemistry, 170(1), 183-185 (1988-04-01)
A method for staining iron proteins on polyacrylamide gel electropherograms is described. It is based upon catalysis, by iron, of the oxidation of diaminobenzoic acid by hydrogen peroxide. Bands containing as little as 5 ng of protein-bound iron can be
Interference of Bis-Tris buffer with the diaminobenzoic acid fluorescence assay used to quantify DNA.
W E Schy et al.
Mutation research, 226(4), 263-266 (1989-08-01)
Superoxide dismutase modification and genotoxicity of transition-metal ion chelators.
T P Coogan et al.
Advances in experimental medicine and biology, 197, 281-290 (1986-01-01)
T R Bosworth et al.
Analytical biochemistry, 223(2), 266-273 (1994-12-01)
Glycosaminoglycan (GAG) hexosamines were measured after deacetylation (2 h acid hydrolysis), deaminative cleavage by nitrous acid, and coupling of the 2,5-anhydro sugars thus produced with 3,5-diaminobenzoic acid (DABA) to give a fluorescent product. Analyses were performed after the addition of

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