D12805
3,5-Diaminobenzoic acid
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:
Molecular Weight:
152.15
Beilstein:
2086484
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
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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 Code
11 - Combustible Solids
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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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
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
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
A rapid fluorometric method for the estimation of DNA in cultured cells.
B G Erwin et al.
Analytical biochemistry, 110(2), 291-294 (1981-01-15)
Pete Crisalli et al.
The Journal of organic chemistry, 78(3), 1184-1189 (2013-01-08)
The formation of oximes and hydrazones is widely used in chemistry and biology as a molecular conjugation strategy for achieving ligation, attachment, and bioconjugation. However, the relatively slow rate of reaction has hindered its utility. Here, we report that simple
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