isononanoyl chloride
Isononanoyl chloride
CAS: 36727-29-4
Molecular Formula: C9H17ClO;C9H17OCl
isononanoyl chloride - Names and Identifiers
| Name | Isononanoyl chloride |
| Synonyms | INCL Isononanoyl chloride 3,5,5-trimethylhexanoyl chloride |
| CAS | 36727-29-4 |
| EINECS | 253-168-4 |
| InChI | InChI=1/C9H17ClO/c1-7(5-8(10)11)6-9(2,3)4/h7H,5-6H2,1-4H3 |
| InChIKey | GEKPNPPFAYJZRD-UHFFFAOYSA-N |
isononanoyl chloride - Physico-chemical Properties
| Molecular Formula | C9H17ClO C9H17OCl |
| Molar Mass | 176.68 |
| Density | 0.949g/cm3 |
| Boling Point | 188.8°C at 760 mmHg |
| Flash Point | 58.2°C |
| Vapor Presure | 0.587mmHg at 25°C |
| Specific Gravity | 0.940 |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.435 |
| MDL | MFCD00044028 |
isononanoyl chloride - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | R14 - Reacts violently with water R20 - Harmful by inhalation R34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | 3389 |
| WGK Germany | 1 |
| RTECS | MP4560000 |
| Hazard Class | 8 |
| Packing Group | III |
isononanoyl chloride - Upstream Downstream Industry
| Raw Materials | 3,5,5-TRIMETHYLHEXANAL 3,5,5-Trimethylhexanoic acid |
| Downstream Products | Piroctone olamine |
isononanoyl chloride - Introduction
Open Data Unverified Data
Isononanoyl chloride(Isononanoyl chloride) is an organic compound with the chemical formula C9H17ClO. Its nature is as follows:
Appearance: colorless liquid
Solubility: Can be dissolved in common organic solvents, such as alcohols, ethers, hydrocarbons, etc.
Melting point:-6 ℃
Boiling point: 199-200 ℃
Density: 0.905g/cm³
Isononanoyl chloride have the following uses in industry:
1. as an intermediate of organic synthetic chemicals, used in the synthesis of organic compounds, such as esters, acid chloride derivatives.
2. Used as a binder and modifier in inks or coatings.
3. used as a synthetic surfactant and functional polymer.
Preparation of Isononanoyl chloride:
Generally, the preparation of Isononanoyl chloride can be obtained by reacting isononanoic acid with thionyl chloride. Specific steps are as follows:
1. Take a certain amount of isononanoic acid and thionyl chloride, add to the reaction vessel, and heat to an appropriate temperature.
2. As the reaction proceeds, the reactants are thoroughly mixed and reacted by stirring.
3. After the reaction, the reaction is cooled and a suitable solvent, such as ether, is added.
4. Filter the precipitate to obtain the pure Isononanoyl chloride product.
Isononanoyl chloride safety information:
1. Isononanoyl chloride is irritating. Rinse with water immediately after contact with skin and eyes and seek medical help.
2. during operation, attention should be paid to protective measures, including wearing gloves, safety glasses and protective clothing.
3. Avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
4. storage should be sealed, dark, well ventilated, stored in a dry, clean place.
Appearance: colorless liquid
Solubility: Can be dissolved in common organic solvents, such as alcohols, ethers, hydrocarbons, etc.
Melting point:-6 ℃
Boiling point: 199-200 ℃
Density: 0.905g/cm³
Isononanoyl chloride have the following uses in industry:
1. as an intermediate of organic synthetic chemicals, used in the synthesis of organic compounds, such as esters, acid chloride derivatives.
2. Used as a binder and modifier in inks or coatings.
3. used as a synthetic surfactant and functional polymer.
Preparation of Isononanoyl chloride:
Generally, the preparation of Isononanoyl chloride can be obtained by reacting isononanoic acid with thionyl chloride. Specific steps are as follows:
1. Take a certain amount of isononanoic acid and thionyl chloride, add to the reaction vessel, and heat to an appropriate temperature.
2. As the reaction proceeds, the reactants are thoroughly mixed and reacted by stirring.
3. After the reaction, the reaction is cooled and a suitable solvent, such as ether, is added.
4. Filter the precipitate to obtain the pure Isononanoyl chloride product.
Isononanoyl chloride safety information:
1. Isononanoyl chloride is irritating. Rinse with water immediately after contact with skin and eyes and seek medical help.
2. during operation, attention should be paid to protective measures, including wearing gloves, safety glasses and protective clothing.
3. Avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
4. storage should be sealed, dark, well ventilated, stored in a dry, clean place.
Last Update：2024-04-09 19:43:38
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Raw Materials for isononanoyl chloride
Downstream Products for isononanoyl chloride