![]() Benzoic acid,3,5-diamino-, hydrochloride (1:2) structure
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Common Name | Benzoic acid,3,5-diamino-, hydrochloride (1:2) | ||
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CAS Number | 618-56-4 | Molecular Weight | 225.07200 | |
Density | N/A | Boiling Point | 459.1ºC at 760 mmHg | |
Molecular Formula | C7H10Cl2N2O2 | Melting Point | >300 °C(lit.) | |
MSDS | USA | Flash Point | 231.5ºC |
A specific fluorometric assay for hexosamines in glycosaminoglycans, based on deaminative cleavage with nitrous acid.
Anal. Biochem. 223(2) , 266-73, (1994) 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... |
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[Improved fluorometric method for DNA microanalysis].
Izv. Akad. Nauk SSSR Biol. (2) , 217-22, (1984)
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Interference of Bis-Tris buffer with the diaminobenzoic acid fluorescence assay used to quantify DNA.
Mutat. Res. 226(4) , 263-6, (1989)
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Simplified isolation and quantitation of cytoplasmic DNA from rat liver.
Anal. Biochem. 103(2) , 413-8, (1980)
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A fluorometric deoxyribonucleic acid assay for tridimensional lattice cultures of fibroblasts.
Anal. Biochem. 210 , 374, (1993) 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... |
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Selective catalysis with peptide dendrimers.
J. Am. Chem. Soc. 126(25) , 7817-26, (2004) Peptide dendrimers incorporating 3,5-diaminobenzoic acid 1 as a branching unit (B) were prepared by solid-phase synthesis of ((Ac-A(3))(2)B-A(2))(2)B-Cys-A(1)-NH(2) followed by disulfide bridge formation. Twenty-one homo- and heterodimeric dendrimers were obt... |
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Superoxide dismutase modification and genotoxicity of transition-metal ion chelators.
Adv. Exp. Med. Biol. 197 , 281-90, (1986)
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Water-soluble organocatalysts for hydrazone and oxime formation.
J. Org. Chem. 78(3) , 1184-9, (2013) 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 ... |
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Reducing the alkali cation adductions of oligonucleotides using sol-gel-assisted laser desorption/ionization mass spectrometry.
Anal. Chem. 75(16) , 4223-8, (2003) The alkali cation adductions of oligonucleotides dramatically degrade MALDI mass spectra and even affect the detection limit. Desalting is generally involved in MALDI sample preparation. This work demonstrates the feasibility of using 3,4-diaminobenzoic acid ... |
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Fluorometric determination of DNA in agarose gels: usefulness for measurement of double-strand breaks in nonlabeled cells by pulsed-field gel electrophoresis.
Radiat. Res. 135(3) , 338-42, (1993) Quantitative measurement of DNA in agarose gels, particularly as needed for measurement of double-strand breaks induced by agents such as radiation, usually involves the use of radioactively labeled DNA. Thus its usefulness is usually limited to growing cells... |