4-AMINOBUTYLPHOSPHONIC ACID
4-AMINOBUTYLPHOSPHONIC ACID
CAS: 35622-27-6
Molecular Formula: C4H12NO3P
4-AMINOBUTYLPHOSPHONIC ACID - Names and Identifiers
| Name | 4-AMINOBUTYLPHOSPHONIC ACID |
| Synonyms | SKL072 (4-Aminobutyl) 4-Aminobutyl-phosphonate 4-aminobutylphosphonicaci 4-AMINOBUTYLPHOSPHONIC ACID Phosphonic acid,P-(4-aMinobutyl)- |
| CAS | 35622-27-6 |
4-AMINOBUTYLPHOSPHONIC ACID - Physico-chemical Properties
| Molecular Formula | C4H12NO3P |
| Molar Mass | 153.12 |
| Density | 1.304±0.06 g/cm3(Predicted) |
| Melting Point | 133-134 °C |
| Boling Point | 344.2±44.0 °C(Predicted) |
| pKa | pK1: 2.55;pK2: 7.55;pK3: 10.9 (25°C) |
| Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
| Use | A - H;Amino Acids;Modified Amino Acids |
4-AMINOBUTYLPHOSPHONIC ACID - 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. |
| UN IDs | 3261 |
| WGK Germany | 3 |
| Hazard Class | 8 |
| Packing Group | III |
4-AMINOBUTYLPHOSPHONIC ACID - Introduction
4-AMINOBUTYLPHOSPHONIC ACID is an organic compound with the chemical formula C12H17IN2. It is a compound structurally similar to pyridine, in which the methyl group and the phenyl group are attached to carbon atoms 1 and 4, respectively, and a chloride cation.
This compound is mainly used as a catalyst and ligand in organic synthesis. It has good catalytic activity and selectivity, and can be used to synthesize organic compounds such as natural products, drugs and functional materials. In addition, it can also be used as a complex of metal ions, and used in organic synthesis reactions such as catalytic reduction reactions and catalytic coupling reactions.
The method for preparing 4-AMINOBUTYLPHOSPHONIC ACID usually involves the amide inclusion reaction of benzyl alcohol and 4-amino -1-methyl pyridine, and then the desired product is obtained through an iodination reaction.
Regarding safety information, due to the lack of clear data, the specific safety and danger are not clear. When handling and using the compound, follow laboratory safety practices, including wearing appropriate protective equipment (such as gloves, glasses, and laboratory coats) to avoid direct skin contact and inhalation. If taken by mistake or inhaled by mistake, seek medical attention immediately. When using this compound, it should be sealed and kept away from flammable materials such as oxygen, acid and organic solvents to avoid the risk of fire and explosion.
This compound is mainly used as a catalyst and ligand in organic synthesis. It has good catalytic activity and selectivity, and can be used to synthesize organic compounds such as natural products, drugs and functional materials. In addition, it can also be used as a complex of metal ions, and used in organic synthesis reactions such as catalytic reduction reactions and catalytic coupling reactions.
The method for preparing 4-AMINOBUTYLPHOSPHONIC ACID usually involves the amide inclusion reaction of benzyl alcohol and 4-amino -1-methyl pyridine, and then the desired product is obtained through an iodination reaction.
Regarding safety information, due to the lack of clear data, the specific safety and danger are not clear. When handling and using the compound, follow laboratory safety practices, including wearing appropriate protective equipment (such as gloves, glasses, and laboratory coats) to avoid direct skin contact and inhalation. If taken by mistake or inhaled by mistake, seek medical attention immediately. When using this compound, it should be sealed and kept away from flammable materials such as oxygen, acid and organic solvents to avoid the risk of fire and explosion.
Last Update：2024-04-09 21:04:16
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View History
4-AMINOBUTYLPHOSPHONIC ACID
ALCLOMETASONE DIPROPIONATE (300 MG)
Glycerin 1-hexadecanoate 2-[(Z)-9-octadecenoate]3-octadecanoate
2-[(2-氰基乙酰基)氨基]-5,6-二氢-4H-环戊烷并[D]噻吩-3-甲酸乙酯
[4-氯-6-[(2-甲基苯基)氨基]-S-三嗪-2-基]-(2-甲基苯基)胺
ZINC SILICOFLUORIDE HEXAHYDRATE
Lithium hydrazide (Li(H3N2)) (9CI)
1-乙基-2-氧代-1,2-二氢苯并[CD]吲哚-6-磺酰氯
7-[(4-氨基苯甲酰)氨基]-4-羟基-3-[[4-[(4-磺酸基苯基)偶氮]苯基]偶氮]萘-2-磺酸二钠
8-(4-CHLOROPHENYLTHIO)GUANOSINE 3',5'-CYCLIC MONOPHOSPHOTHIOATE, RP-ISOMER TRIETHYLAMMONIUM SALT
ALCLOMETASONE DIPROPIONATE (300 MG)
Glycerin 1-hexadecanoate 2-[(Z)-9-octadecenoate]3-octadecanoate
2-[(2-氰基乙酰基)氨基]-5,6-二氢-4H-环戊烷并[D]噻吩-3-甲酸乙酯
[4-氯-6-[(2-甲基苯基)氨基]-S-三嗪-2-基]-(2-甲基苯基)胺
ZINC SILICOFLUORIDE HEXAHYDRATE
Lithium hydrazide (Li(H3N2)) (9CI)
1-乙基-2-氧代-1,2-二氢苯并[CD]吲哚-6-磺酰氯
7-[(4-氨基苯甲酰)氨基]-4-羟基-3-[[4-[(4-磺酸基苯基)偶氮]苯基]偶氮]萘-2-磺酸二钠
8-(4-CHLOROPHENYLTHIO)GUANOSINE 3',5'-CYCLIC MONOPHOSPHOTHIOATE, RP-ISOMER TRIETHYLAMMONIUM SALT