1-hexyl-1H-imidazole
Diisooctylphosphinic acid
CAS: 83411-71-6
Molecular Formula: C16H35O2P
1-hexyl-1H-imidazole - Names and Identifiers
| Name | Diisooctylphosphinic acid |
| Synonyms | Cyanex 272 Ionquest 290 1-hexyl-1H-imidazole Diisooctylphosphinic acid DIISOOCTYLPHOSPHINIC ACID Bis(2,4,4-trimethylpentyl)phosphinsure bis(2,4,4-trimethylpentyl)-phosphinicaci Bis(2,4,4-trimethylpentyl)phosphinic acid Bis-(2,4,4-trimethylpentyl)-phosphinic Acid Phosphinic acid,bis(2,4,4-triMethylpentyl)- Phosphinic acid, P,P-bis(2,4,4-trimethylpentyl)- |
| CAS | 83411-71-6 |
| EINECS | 280-445-7 |
| InChI | InChI=1/C9H16N2/c1-2-3-4-5-7-11-8-6-10-9-11/h6,8-9H,2-5,7H2,1H3 |
1-hexyl-1H-imidazole - Physico-chemical Properties
| Molecular Formula | C16H35O2P |
| Molar Mass | 290.42 |
| Density | 0.916g/mLat 20°C(lit.) |
| Boling Point | 417.1±14.0 °C(Predicted) |
| Flash Point | 117°C |
| Vapor Presure | 0.0117mmHg at 25°C |
| Appearance | Crystalline powder |
| pKa | 3.26±0.50(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | n20/D 1.460 |
1-hexyl-1H-imidazole - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36 - Irritating to the eyes |
| Safety Description | S24 - Avoid contact with skin. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| WGK Germany | 1 |
| HS Code | 29319090 |
1-hexyl-1H-imidazole - Introduction
Diisooctylphosphinic acid is an organophosphorus compound with the chemical formula [(CH3)2C(CH3)2]2P(OH). The following is an introduction to its nature, use, preparation and safety information:
Nature:
-Appearance: Diisooctylphosphinic acid is generally colorless to yellow liquid, similar to the appearance of the paste.
-Solubility: It is soluble in organic solvents, such as ether, ethanol and benzene.
-Stability: Diisooctylphosphinic acid is relatively stable at room temperature, but may decompose at high temperature.
Use:
-Catalyst: Diisooctylphosphinic acid can be used as a ligand for negative oxidants and is used for catalytic reactions in organic synthesis, such as asymmetric hydrogenation, nucleophilic addition reactions of alkenes catalyzed by nitrogen and nitrogen benzene.
-Fluorescent probe: Diisooctylphosphinic acid has certain fluorescent properties and can be used as a fluorescent probe in the field of biochemical analysis.
Preparation Method:
The preparation of Diisooctylphosphinic acid is usually carried out by the following steps:
1. trimethyl pentyl alcohol was synthesized from trimethyl pentyl phosphine chloride (CH3)3 CPCl2.
2. reacting trimethylpentylphosphine chloride with water to generate trimethylpentylphosphonic acid (CH3)3CP(O)OH.
Safety Information:
- Diisooctylphosphinic acid is less toxic. But as an organic phosphorus compound, it may cause some degree of harm to the human body.
-When using Diisooctylphosphinic acid, you need to take appropriate laboratory safety measures, such as wearing protective glasses and gloves, and operating in a well-ventilated place.
-Avoid direct contact with the skin to avoid irritation or allergic reactions.
-When disposing of waste, it needs to be disposed of in accordance with local regulations.
Nature:
-Appearance: Diisooctylphosphinic acid is generally colorless to yellow liquid, similar to the appearance of the paste.
-Solubility: It is soluble in organic solvents, such as ether, ethanol and benzene.
-Stability: Diisooctylphosphinic acid is relatively stable at room temperature, but may decompose at high temperature.
Use:
-Catalyst: Diisooctylphosphinic acid can be used as a ligand for negative oxidants and is used for catalytic reactions in organic synthesis, such as asymmetric hydrogenation, nucleophilic addition reactions of alkenes catalyzed by nitrogen and nitrogen benzene.
-Fluorescent probe: Diisooctylphosphinic acid has certain fluorescent properties and can be used as a fluorescent probe in the field of biochemical analysis.
Preparation Method:
The preparation of Diisooctylphosphinic acid is usually carried out by the following steps:
1. trimethyl pentyl alcohol was synthesized from trimethyl pentyl phosphine chloride (CH3)3 CPCl2.
2. reacting trimethylpentylphosphine chloride with water to generate trimethylpentylphosphonic acid (CH3)3CP(O)OH.
Safety Information:
- Diisooctylphosphinic acid is less toxic. But as an organic phosphorus compound, it may cause some degree of harm to the human body.
-When using Diisooctylphosphinic acid, you need to take appropriate laboratory safety measures, such as wearing protective glasses and gloves, and operating in a well-ventilated place.
-Avoid direct contact with the skin to avoid irritation or allergic reactions.
-When disposing of waste, it needs to be disposed of in accordance with local regulations.
Last Update：2024-04-10 22:29:15
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View History
1-hexyl-1H-imidazole
2-PyriMidinaMine, N-(2-Methyl-4-nitrophenyl)-4-(3-pyridinyl)-
IXABEPILONE
7-Oxabicyclo[4.1.0]heptane, 4-[1-(chloromethyl)ethenyl]-1-methyl-, (4S)-
2-甲基-5-乙酰基嘧啶
2-溴-4-甲基苯-1-碳硫酰胺
Poly(oxy(dimethylsilylene)), alpha-(trimethylsilyl)-omega-((trimethylsilyl)oxy)-
3-Isoquinolinecarboxylic acid (6CI,9CI)
METHYL 5-(2-CHLOROPHENYL)PIPERIDINE-2-CARBOXYLATE HYDROCHLORIDE
1-(3-氟-4-甲基苯基)环丙烷-1-胺盐酸盐
2-PyriMidinaMine, N-(2-Methyl-4-nitrophenyl)-4-(3-pyridinyl)-
IXABEPILONE
7-Oxabicyclo[4.1.0]heptane, 4-[1-(chloromethyl)ethenyl]-1-methyl-, (4S)-
2-甲基-5-乙酰基嘧啶
2-溴-4-甲基苯-1-碳硫酰胺
Poly(oxy(dimethylsilylene)), alpha-(trimethylsilyl)-omega-((trimethylsilyl)oxy)-
3-Isoquinolinecarboxylic acid (6CI,9CI)
METHYL 5-(2-CHLOROPHENYL)PIPERIDINE-2-CARBOXYLATE HYDROCHLORIDE
1-(3-氟-4-甲基苯基)环丙烷-1-胺盐酸盐