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Cat. No.: HY-N7125R

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Cinnamyl acetate (Standard)

Name: Cinnamyl acetate (Standard)
Brand: MedChemExpress
SKU: HY-N7125R
Price: 53.00 USD
Availability: InStock
Rating: 5 (1 reviews)

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Cinnamyl acetate (Standard) is the analytical standard of Cinnamyl acetate (HY-N7125). This product is intended for research and analytical applications. Cinnamyl acetate is a phenylpropanoid ester fragrance ingredient that serves as a precursor for the synthesis of Chloramphenicol (HY-B0239) and butyrolactone costunolide, and possesses antioxidant activity. Cinnamyl acetate is used in the food, cosmetics, personal care, and pharmaceutical industries.

For research use only. We do not sell to patients.

CAS No.: 103-54-8
Formula: C₁₁H₁₂O₂
Molecular Weight:176.21

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Cinnamyl acetate (Standard) Chemical Structure

CAS No.: 103-54-8

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

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Product Information

Information

Application

The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.

Chemical Information

CAS No. 103-54-8
Appearance Liquid
Molecular Weight 176.21
Formula C₁₁H₁₂O₂
Color Colorless to light yellow
SMILES

CC(OC/C=C/C1=CC=CC=C1)=O
Structure Classification
- Phenylpropanoids
- Simple Phenylpropanols
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
COA (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Qinghua Liang, et al. Theoretical and experimental studies on the separation of cinnamyl acetate and cinnamaldehyde by adsorption onto a β-cyclodextrin polyurethane polymer. RSC Adv. 2017; 7 (69): 43502–43511.

[2]. Tomke PD, et al. Ultrasound assisted lipase catalyzed synthesis of cinnamyl acetate via transesterification reaction in a solvent free medium. Ultrasonics sonochemistry. 2015 Nov;27:241-246.

[3]. Dong H, et al. Whole-Cell Biocatalytic Synthesis of Cinnamyl Acetate with a Novel Esterase from the DNA Library of Acinetobacter hemolyticus. Journal of agricultural and food chemistry. 2017 Mar 15;65(10):2120-2128. [Content Brief]

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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