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4-Acetoxycinnamic acid
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 4-Acetoxycinnamic acid
Price: $30 / 20mg
CAS No.: 15486-19-8
Catalog No.: CFN98178
Molecular Formula: C11H10O4
Molecular Weight: 206.19 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Powder
Source: The barks of Cinnamomum cassia Presl
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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4-Acetoxycinnamic acid Description
Source: The barks of Cinnamomum cassia Presl
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.8499 mL 24.2495 mL 48.499 mL 96.9979 mL 121.2474 mL
5 mM 0.97 mL 4.8499 mL 9.6998 mL 19.3996 mL 24.2495 mL
10 mM 0.485 mL 2.4249 mL 4.8499 mL 9.6998 mL 12.1247 mL
50 mM 0.097 mL 0.485 mL 0.97 mL 1.94 mL 2.4249 mL
100 mM 0.0485 mL 0.2425 mL 0.485 mL 0.97 mL 1.2125 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Macromolecules, 2003, 36(20).
Self-Organizing Polycondensation of (E)-4-Acetoxycinnamic Acid for Preparation of Poly(p-oxycinnamoyl) Microspheres.[Reference: WebLink]

METHODS AND RESULTS:
Preparation of poly(p-oxycinnamoyl) (POC) microspheres was examined by the reaction-induced phase separation of oligomers during the polycondensation of (E)-4-Acetoxycinnamic acid in various solvents. Polymerization in liquid paraffin yielded the microspheres having a smooth surface at 270−330 °C, of which the average diameter was 4.6 μm. In contrast to this, the morphology of the products was drastically changed in Therm S 800 (TS8) and Therm S 900 (TS9) by polymerization temperature. When the polymerization was carried out at 310 °C in TS8 and 300 °C in TS9, the microspheres were obtained, of which the average diameter was 3.9 and 3.3 μm, respectively. The platelike crystals were formed under these temperatures, of which thickness was approximately 0.1 μm. The formation of the microspheres was highly related to the miscibility between the oligomers and the solvents. The average diameter of the microspheres increased with the decrease of the miscibility, and this tendency could be accounted for by the interfacial tension between two immiscible liquid phases.
CONCLUSIONS:
The microspheres were formed through the formation of the microdroplets by the liquid−liquid phase separation of the oligomers and the subsequent solidification of the microdroplets due to the further polymerization in them.
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