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113832

Sigma-Aldrich

3,5-Diaminobenzoic acid dihydrochloride

99%

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About This Item

Linear Formula:
(H2N)2C6H3CO2H·2HCl
CAS Number:
618-56-4
Molecular Weight:
225.07
Beilstein:
3703362
EC Number:
210-556-8
MDL number:
MFCD00012983
UNSPSC Code:
12352200
PubChem Substance ID:
24847151
NACRES:
NA.22

Assay

99%

reaction suitability

reaction type: solution phase peptide synthesis

mp

>300 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cl[H].Cl[H].Nc1cc(N)cc(c1)C(O)=O

InChI

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

InChI key

IGPLRBRBTUNCRT-UHFFFAOYSA-N

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Application

Uses include the fluorometric microdetermination of DNA.[1]

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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Certificates of Analysis (COA)

Lot/Batch Number
19322CY
05128PV
S35171
34880

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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
R J Wilkins et al.
Analytical biochemistry, 136(2), 301-308 (1984-02-01)
Procedures for collecting DNA from dilute solutions as small spots of the insoluble cetyltrimethylammonium salt deposited on either glass fiber or Millipore filters are described. This method of concentration facilitates the fluorescent assay of DNA, either by a microreaction in
A rapid in situ deoxyribonucleic acid assay for determining cell number in culture and tissue.
B Johnson-Wint et al.
Analytical biochemistry, 122(2), 338-344 (1982-05-15)
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)
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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