Identification | More | [Name]
2-AMINOPYRIDINE-5-SULFONIC ACID | [CAS]
16250-08-1 | [Synonyms]
2-AMINOPYRIDINE-5-SULFONIC ACID 2-AMINOPYRIDINE-5-SULPHONIC ACID 6-AMINOPYRIDINE-3-SULFONIC ACID AKOS BBS-00001355 AURORA 12418 OTAVA-BB BB0111070132 2-AMINO-5-PYRIDINESULFONIC ACID 6-Amino-3-pyridinesulfonic Acid Pyridin-2-amino-5-sulfonic Acid Pyridine-2-amino-5-sulfonic Acid | [Molecular Formula]
C5H6N2O3S | [MDL Number]
MFCD00160315 | [Molecular Weight]
174.18 | [MOL File]
16250-08-1.mol |
Chemical Properties | Back Directory | [Appearance]
Off-Whie Solid | [Melting point ]
>300°C | [density ]
1.617 | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
-1?+-.0.50(Predicted) | [color ]
White to Off-White | [CAS DataBase Reference]
16250-08-1(CAS DataBase Reference) |
Hazard Information | Back Directory | [Chemical Properties]
Off-Whie Solid | [Synthesis]
The general procedure for the synthesis of 6-aminopyridine-3-sulfonic acid from 2-aminopyridine was as follows: (i) 2-aminopyridine (80 g, 0.85 mol) was added to fuming sulfuric acid (320 g) in batches over 30 minutes. Subsequently, the resulting reaction mixture was heated and reacted at 140°C for 4 hours. After completion of the reaction, it was cooled to room temperature, the reaction was slowly poured into ice (200 g) and stirring was continued for 2 hours under ice/salt bath conditions. The resulting suspension was separated by filtration and the solids were washed sequentially with ice water (200 mL) and cold industrial methylated alcohol (IMS, 200 mL). Finally, the pyridine-2-amino-5-sulfonic acid solid product (111.3 g) was obtained by filtration drying. lRMS (Thermospray) analysis result: m/z 175 (M + 1)+. | [References]
[1] Patent: US6440982, 2002, B1 [2] Patent: US6251904, 2001, B1 [3] Zhurnal Russkago Fiziko-Khimicheskago Obshchestva, 1920, vol. 50, p. 495 [4] Chem. Zentralbl., 1923, vol. 94, # III, p. 1021 [5] Bulletin de la Societe Chimique de France, 1939, vol. <5> 6, p. 736,738 |
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