N-氨基碘化吡啶
1-Aminopyridinium iodide
CAS: 6295-87-0
Molecular Formula: C5H7IN2
N-氨基碘化吡啶 - Names and Identifiers
| Name | 1-Aminopyridinium iodide |
| Synonyms | pyridin-1-amine 1-aminopyridinium pyridinium-1-ylazanide Aminopyridinium iodide N-AMINOPYRIDINIUM IODIDE 1-Aminopyridinium iodide 1-AMINOPYRIDINIUM IODIDE Pyridin-1-ium-1-amine iodide Pyridinium, 1-amino-, iodide |
| CAS | 6295-87-0 |
| EINECS | 228-566-6 |
| InChI | InChI=1/C5H7N2.HI/c6-7-4-2-1-3-5-7;/h1-5H,6H2;1H/q+1;/p-1 |
| InChIKey | NDRLPYIMWROJBG-UHFFFAOYSA-M |
N-氨基碘化吡啶 - Physico-chemical Properties
| Molecular Formula | C5H7IN2 |
| Molar Mass | 222.03 |
| Density | 1.8200 (estimate) |
| Melting Point | 159-161°C(lit.) |
| Water Solubility | Soluble in water (almost transparency). |
| Appearance | powder to crystal |
| Color | White to Light yellow to Light orange |
| Exposure Limit | ACGIH: TWA 0.01 ppm |
| BRN | 3713241 |
| Storage Condition | 2-8°C |
| Sensitive | Light Sensitive |
| MDL | MFCD00051893 |
N-氨基碘化吡啶 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 8-10-21 |
| HS Code | 29333990 |
N-氨基碘化吡啶 - Introduction
1-Aminopyridinium iodide(1-Aminopyridinium iodide) is an organic compound with a chemical formula of C5H6IN2 and a molecular weight of 248.01g/mol. It is a white crystalline powder with a weak smelly ammonia smell.
1-Aminopyridinium iodide has diverse applications in organic synthesis. It can be used as a starting material for catalysts, oxidizing and reducing agents and as an anion exchanger. Commonly used in organic synthesis reaction of nitrogen and iodine activation, alkyne anionic polymerization and aromatization reaction.
The preparation of 1-Aminopyridinium iodide is usually obtained by the substitution reaction of pyridine. The most common method is the reaction of 1-amino -2, 3-lutidine with iodine and an acid.
For safety information, 1-Aminopyridinium iodide should be considered hazardous. It is irritating and contact with the skin and eyes may cause irritation and burns. Wear appropriate protective equipment, such as gloves and goggles, and operate in a well-ventilated area.
1-Aminopyridinium iodide has diverse applications in organic synthesis. It can be used as a starting material for catalysts, oxidizing and reducing agents and as an anion exchanger. Commonly used in organic synthesis reaction of nitrogen and iodine activation, alkyne anionic polymerization and aromatization reaction.
The preparation of 1-Aminopyridinium iodide is usually obtained by the substitution reaction of pyridine. The most common method is the reaction of 1-amino -2, 3-lutidine with iodine and an acid.
For safety information, 1-Aminopyridinium iodide should be considered hazardous. It is irritating and contact with the skin and eyes may cause irritation and burns. Wear appropriate protective equipment, such as gloves and goggles, and operate in a well-ventilated area.
Last Update：2024-04-10 22:29:15
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View History
N-氨基碘化吡啶
甲氧基二苯基磷
METHYL 2-(4-([(3-BROMOPHENYL)SULFONYL]AMINO)PHENOXY)BENZENECARBOXYLATE
3-[(Z)-ANILINOMETHYLIDENE]-2H-CHROMENE-2,4-DIONE
3-(1-萘基)丙烯酸
6-C-alpha-L-Arabinosyl-8-C-beta-D-glucosylapigenin
2-Mercapo-5-difluoromethoxy benzimidazole
4-溴苯甲酰甲基三氟甲磺酸酯
5-氨基-6-碘吡啶-2-羧酸乙酯
2-[(2-fluoro-5-methylanilino)carbonyl]cyclopropanecarboxylic acid
甲氧基二苯基磷
METHYL 2-(4-([(3-BROMOPHENYL)SULFONYL]AMINO)PHENOXY)BENZENECARBOXYLATE
3-[(Z)-ANILINOMETHYLIDENE]-2H-CHROMENE-2,4-DIONE
3-(1-萘基)丙烯酸
6-C-alpha-L-Arabinosyl-8-C-beta-D-glucosylapigenin
2-Mercapo-5-difluoromethoxy benzimidazole
4-溴苯甲酰甲基三氟甲磺酸酯
5-氨基-6-碘吡啶-2-羧酸乙酯
2-[(2-fluoro-5-methylanilino)carbonyl]cyclopropanecarboxylic acid