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D12805

3,5-Diaminobenzoic acid

Name: 3,5-Diaminobenzoic acid
Brand: ALDRICH

98%, for peptide synthesis

Synonym(s):

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

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About This Item

Linear Formula:

(H₂N)₂C₆H₃CO₂H

CAS Number:

535-87-5

Molecular Weight:

152.15

NACRES:

NA.22

PubChem Substance ID:

24893395

UNSPSC Code:

12352106

EC Number:

208-621-0

MDL number:

MFCD00007807

Beilstein/REAXYS Number:

2086484

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Properties

Product Name

3,5-Diaminobenzoic acid, 98%

Quality Level

100

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

Description

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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A fluorometric deoxyribonucleic acid assay for tridimensional lattice cultures of fibroblasts.

P Gillery et al.

Analytical biochemistry, 210(2), 374-377 (1993-05-01)

A fast and sensitive in situ assay of deoxyribonucleic acid in miniaturized lattice cultures of fibroblasts is described. Tridimensional collagen and fibrin lattices prepared in 24-well plates were seeded with 50,000 to 200,000 cells. Cultures were fixed with formaldehyde, rinced

Use of the diaminobenzoic acid fluorescence assay in conjunction with uv absorbance as a means of quantifying and ascertaining the purity of a DNA preparation.

W E Schy et al.

Analytical biochemistry, 180(2), 314-318 (1989-08-01)

In the course of a study conducted to determine the correlation between covalently bound DNA-ethyl adducts and specific locus mutation induction in maize (W. E. Schy and M. J. Plewa Mutat. Res., 211, 231-241), it was necessary to accurately quantify

Transaminations catalysed by brain glutamate decarboxylase.

T G Porter et al.

The Biochemical journal, 231(3), 705-712 (1985-11-01)

In addition to normal decarboxylation of glutamate to 4-aminobutyrate, glutamate decarboxylase from pig brain was shown to catalyse decarboxylation-dependent transamination of L-glutamate and direct transamination of 4-aminobutyrate with pyridoxal 5'-phosphate to yield succinic semialdehyde and pyridoxamine 5'-phosphate in a 1:1

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Global Trade Item Number

SKU	GTIN
D12805-1KG	04061826107607
D12805-100G	04061833559239