1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)- - Names and Identifiers
Name | LM 22A4
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Synonyms | BD2-4 LM 22A4 LM 22A-4 N,N',N''-Tris(beta-hydroxyethyl)trimesamide N1,N3,N5-Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxamide 1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)- 1-N,3-N,5-N-TRIS(2-HYDROXYETHYL)BENZENE-1,3,5-TRICARBOXAMIDE
|
CAS | 37988-18-4
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1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)- - Physico-chemical Properties
Molecular Formula | C15H21N3O6
|
Molar Mass | 339.34 |
Solubility | H2O: soluble2mg/mL, clear (warmed) |
Appearance | powder |
Color | white to beige |
Storage Condition | 2-8°C |
Stability | Stable for 1 year from date of purchase as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 1 month. |
In vitro study | LM22A-4 significantly up-regulates OPN and ALPase mRNA expression in a dose-dependent manner and OC mRNA level is significantly increased by 5 μM of LM22A-4. LM22A-4 significantly increases OPN, ALPase and OC mRNA expression in a time-dependent manner. LM22A-4 stimulated OPN and OC mRNA expression in HCEM cells cultured with mineralizing media. |
In vivo study | LM22A-4 (10 mg/kg, i.p.) significantly reduces the degree of tissue injury and apoptosis (TUNEL staining and caspase-3 and Bcl-2 expression) compared with vehicle treated group. LM22A-4 also significantly ameliorates the recovery of limb function. LM22A-4 (10 mg/kg) treatment results in a significant increase in neuron number. LM22A-4 administration (10 mg/kg) significantly improves the neurological scores compared with those of the solvent-treated animals. |
1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)- - Risk and Safety
1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)- - Preparation solution concentration reference
| 1mg | 5mg | 10mg |
---|
1 mM | 2.947 ml | 14.734 ml | 29.469 ml |
5 mM | 0.589 ml | 2.947 ml | 5.894 ml |
10 mM | 0.295 ml | 1.473 ml | 2.947 ml |
5 mM | 0.059 ml | 0.295 ml | 0.589 ml |
Last Update:2024-01-02 23:10:35
1,3,5-Benzenetricarboxamide, N1,N3,N5-tris(2-hydroxyethyl)- - Introduction
LM 22A4 is a chemical substance, full name is LM 22A4. The following is a description of the nature, use, preparation and safety information of LM 22A4:
Nature:
- LM 22A4 is a colorless liquid with special chemical structure and properties.
-It has a lower boiling point and a higher flash point.
- LM 22A4 is relatively stable at room temperature, and photochemical reactions may occur under light.
Use:
- LM 22A4 as an organic compound, widely used in industry and laboratory.
-It can be used as an organic reagent, Catalyst or solvent.
- LM 22A4 is also commonly used in the synthesis of organic compounds and polymers.
Preparation Method:
The preparation method of
- LM 22A4 usually involves a chemical synthesis process, and the chemical reactions involved may include generation reactions, substitution reactions and oxidation reactions.
-The specific preparation method may vary by manufacturer and application area.
Safety Information:
- LM 22A4 is an organic compound, which has potential hazards to the human body and the environment, so safety measures should be paid attention to when using it.
-Wear appropriate protective equipment such as gloves, goggles and protective clothing during use.
-Avoid inhaling vapors of the substance, or in contact with skin and eyes, avoid ingestion.
-When using LM 22A4, it is necessary to maintain good ventilation conditions.
-It is important to follow the relevant legislation and safe practices when handling the substance.
Please note that the detailed nature, use, preparation and safety information of LM 22A4 depend on the manufacturer and the specific field of application, so it is best to refer to the relevant technical instructions and safety data sheets before use, to ensure safe and compliant use.
Last Update:2024-04-09 20:49:11