22884-29-3
isobutyltriphenylphosphonium bromide
CAS: 22884-29-3
Molecular Formula: C22H24BrP
22884-29-3 - Names and Identifiers
| Name | isobutyltriphenylphosphonium bromide |
| Synonyms | PA24 PA24A PLA2G4 Cytosolic phospholipase A2 HIV-1 Tat interactive protein histone acetyltransferase HTATIP Isobutyltriphenylphosphonium bromide isobutyltriphenylphosphonium bromide cytosolic phospholipase A2 γ precursor Anti-C-PLA2 antibody produced in rabbit (2-methylpropyl)(triphenyl)phosphonium bromide |
| CAS | 22884-29-3 |
| EINECS | 245-291-7 |
| InChI | InChI=1/C22H24P.BrH/c1-19(2)18-23(20-12-6-3-7-13-20,21-14-8-4-9-15-21)22-16-10-5-11-17-22;/h3-17,19H,18H2,1-2H3;1H/q+1;/p-1 |
22884-29-3 - Physico-chemical Properties
| Molecular Formula | C22H24BrP |
| Molar Mass | 399.31 |
| Melting Point | 200-202°C(lit.) |
| Appearance | solid |
| BRN | 4171228 |
| Storage Condition | Inert atmosphere,Room Temperature |
| Sensitive | Hygroscopic |
| MDL | MFCD00031593 |
22884-29-3 - 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. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
| HS Code | 29310099 |
22884-29-3 - Introduction
Brmide (Brmide) is an organic compound. The following is information about the properties, use, preparation and safety of the compound:
Nature:
-Appearance: bromide is a white or yellowish-white solid.
-Solubility: It has good solubility in organic solvents, such as dimethylformamide, acetonitrile and dichloromethane.
-Melting point: Its melting point is usually between 130-132°C.
Use:
-bromide is a commonly used reagent, often used in organic synthesis reaction.
-It can be used as an alkylation reagent to introduce alkyl groups in organic synthesis.
-The compound can also be used as a photosensitive reagent for photochemical reactions and the preparation of organic photoelectric conversion devices.
Method: The preparation of
-bromide is usually obtained by reacting triphenylphosphine with bromoisopropanol. The specific reaction conditions can be optimized according to actual needs.
Safety Information:
-bromide has a certain toxicity, should avoid direct contact with the skin and inhalation.
-Use with appropriate protective measures, including gloves, goggles and lab coats.
-In the event of inadvertent contact or inhalation of the substance, immediately rinse the affected area and seek medical help.
-Waste disposal should follow local regulations and should not be discarded into the environment.
Please note that this information is only for reference, and the specific nature, use, preparation method and safety requirements may need to be further confirmed and adjusted according to specific experimental conditions and operating requirements.
Nature:
-Appearance: bromide is a white or yellowish-white solid.
-Solubility: It has good solubility in organic solvents, such as dimethylformamide, acetonitrile and dichloromethane.
-Melting point: Its melting point is usually between 130-132°C.
Use:
-bromide is a commonly used reagent, often used in organic synthesis reaction.
-It can be used as an alkylation reagent to introduce alkyl groups in organic synthesis.
-The compound can also be used as a photosensitive reagent for photochemical reactions and the preparation of organic photoelectric conversion devices.
Method: The preparation of
-bromide is usually obtained by reacting triphenylphosphine with bromoisopropanol. The specific reaction conditions can be optimized according to actual needs.
Safety Information:
-bromide has a certain toxicity, should avoid direct contact with the skin and inhalation.
-Use with appropriate protective measures, including gloves, goggles and lab coats.
-In the event of inadvertent contact or inhalation of the substance, immediately rinse the affected area and seek medical help.
-Waste disposal should follow local regulations and should not be discarded into the environment.
Please note that this information is only for reference, and the specific nature, use, preparation method and safety requirements may need to be further confirmed and adjusted according to specific experimental conditions and operating requirements.
Last Update：2024-04-09 15:17:56
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View History
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