Palmitic acid N-hydroxysuccinimide ester
N-succinimidyl palmitate
CAS: 14464-31-4
Molecular Formula: C20H35NO4
Palmitic acid N-hydroxysuccinimide ester - Names and Identifiers
| Name | N-succinimidyl palmitate |
| Synonyms | PAL-OSU HEXADECANOIC ACID-NHSE N-succinimidyl palmitate N-SUCCINIMIDYL PALMITATE N-(PALMITOYLOXY)SUCCINIMIDE 1-Palmitoyl-N-hydroxysuccinimide 1-PALMITOYL-N-HYDROXYSUCCINIMIDE PALMITIC ACID N-HYDROXYSUCCINIMIDE PALMITIC ACID N-SUCCINIMIDYL ESTER Palmitic acid N-hydroxysuccinimide ester 1-(hexadecanoyloxy)pyrrolidine-2,5-dione PALMITIC ACID N-HYDROXY-SUCCINIMIDE ESTER |
| CAS | 14464-31-4 |
| InChI | InChI=1/C20H35NO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(24)25-21-18(22)16-17-19(21)23/h2-17H2,1H3 |
Palmitic acid N-hydroxysuccinimide ester - Physico-chemical Properties
| Molecular Formula | C20H35NO4 |
| Molar Mass | 353.5 |
| Density | 1.03±0.1 g/cm3(Predicted) |
| Melting Point | 81°C |
| Boling Point | 447.1±28.0 °C(Predicted) |
| Flash Point | 224.2°C |
| Solubility | Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) |
| Vapor Presure | 3.45E-08mmHg at 25°C |
| Appearance | Colorless and glossy sheet |
| Color | White to Off-White |
| BRN | 1547411 |
| Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
| Stability | Moisture Sensitive; Store in Freezer |
| Refractive Index | 1.488 |
Palmitic acid N-hydroxysuccinimide ester - Risk and Safety
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10 |
Palmitic acid N-hydroxysuccinimide ester - Reference
| Reference Show more | 1. [IF=10.317] Ting Gong et al."Palmitic acid-modified bovine serum albumin nanoparticles target scavenger receptor-A on activated macrophages to treat rheumatoid arthritis."Biomaterials. 2020 Nov;258:120296 |
Palmitic acid N-hydroxysuccinimide ester - Introduction
N-succinimidyl palmitate(Palmitic acid N-hydroxysuccinimide ester) is a compound with the chemical structure C16H31CONHSO2CH2CO. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: brownish-orange to light yellow solid.
-Solubility: Soluble in some organic solvents, such as chloroform, ether, methanol, etc.
-Melting point: About 30-50 ° C.
-Stability: Stable to acid, alkali and heat.
Use:
-Biochemical Research: N-succinimidyl palmitate is often used as an active compound and plays an important role in the modification of biologically active molecules.
-Chemical synthesis: As an activator, it can be used in esterification, etherification, amidation and other reactions to promote the reaction.
-Drug development: In drug synthesis, the compound can be used as an activator or intermediate to help synthesize compounds with specific biological activities.
-Surfactant: In some applications, N-succinimidyl palmitate can be used as a surfactant, which has the ability to form micelles.
Method:
The synthesis of N-succinimidyl palmitate can be obtained by the reaction of palmitic acid with hydroxysuccinimide. In the reaction, the two are reacted in a molar ratio of 1:1, and the reaction is carried out in a suitable solvent at a suitable temperature to produce the target product.
Safety Information:
- N-succinimidyl palmitate is irritating and contact with the skin may cause irritation or allergic reactions. During use, wear appropriate protective gloves and glasses to avoid skin and eye contact.
-During storage and transportation, avoid contact with harmful substances such as strong oxidants and strong acids.
-When using and handling, should follow the relevant safety operation procedures and regulations.
Please note that this is only a general introduction to the N-succinimidyl palmitate, and specific nature, use, formulation and safety information may require more detailed information and experimental requirements.
Nature:
-Appearance: brownish-orange to light yellow solid.
-Solubility: Soluble in some organic solvents, such as chloroform, ether, methanol, etc.
-Melting point: About 30-50 ° C.
-Stability: Stable to acid, alkali and heat.
Use:
-Biochemical Research: N-succinimidyl palmitate is often used as an active compound and plays an important role in the modification of biologically active molecules.
-Chemical synthesis: As an activator, it can be used in esterification, etherification, amidation and other reactions to promote the reaction.
-Drug development: In drug synthesis, the compound can be used as an activator or intermediate to help synthesize compounds with specific biological activities.
-Surfactant: In some applications, N-succinimidyl palmitate can be used as a surfactant, which has the ability to form micelles.
Method:
The synthesis of N-succinimidyl palmitate can be obtained by the reaction of palmitic acid with hydroxysuccinimide. In the reaction, the two are reacted in a molar ratio of 1:1, and the reaction is carried out in a suitable solvent at a suitable temperature to produce the target product.
Safety Information:
- N-succinimidyl palmitate is irritating and contact with the skin may cause irritation or allergic reactions. During use, wear appropriate protective gloves and glasses to avoid skin and eye contact.
-During storage and transportation, avoid contact with harmful substances such as strong oxidants and strong acids.
-When using and handling, should follow the relevant safety operation procedures and regulations.
Please note that this is only a general introduction to the N-succinimidyl palmitate, and specific nature, use, formulation and safety information may require more detailed information and experimental requirements.
Last Update：2024-04-09 15:17:52
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View History
Palmitic acid N-hydroxysuccinimide ester
5'-O-(4,4-二甲氧基三苯甲基)-2'-O-甲基尿苷-3'-(2-氰基乙基-N,N-二异丙基)亚磷酰胺
1-{[4-(acetylamino)phenyl]sulfonyl}-1',4-bipiperidine-4-carboxamide
PLATINUM ETHYLENEDIAMINE DICHLORIDE
1-Pyrrolidinecarboxylic acid, 2-ethenyl-, ethyl ester, (2S)-
N,N-Dimethyl-4-{[4-(trifluoromethyl)pyrimidin-2-yl]oxy}benzenesulphonamide
2-Ethyl-2-imidazoline
2-(2-甲烷酰吡咯-1-基)乙酸
羟苯磺酸钙羟苯磺酸钙
MONOMETHYL PENTANE-1,5-DIOATE
5'-O-(4,4-二甲氧基三苯甲基)-2'-O-甲基尿苷-3'-(2-氰基乙基-N,N-二异丙基)亚磷酰胺
1-{[4-(acetylamino)phenyl]sulfonyl}-1',4-bipiperidine-4-carboxamide
PLATINUM ETHYLENEDIAMINE DICHLORIDE
1-Pyrrolidinecarboxylic acid, 2-ethenyl-, ethyl ester, (2S)-
N,N-Dimethyl-4-{[4-(trifluoromethyl)pyrimidin-2-yl]oxy}benzenesulphonamide
2-Ethyl-2-imidazoline
2-(2-甲烷酰吡咯-1-基)乙酸
羟苯磺酸钙羟苯磺酸钙
MONOMETHYL PENTANE-1,5-DIOATE