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Art. -Nr.: HY-N7125S

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Cinnamyl acetate-¹³C₂

Cinnamyl acetate-¹³C₂ is the ¹³C-labeled Cinnamyl acetate (HY-N7125). 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.

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CAS. Nr.: 1083053-34-2
Formel: C₉¹³C₂H₁₂O₂
Molecular Weight:178.20

Speicherung:

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

Data Sheet (273 KB)

Cinnamyl acetate-¹³C₂ Chemical Structure

CAS. Nr.: 1083053-34-2

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Use of MCE Products

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

Biologische Aktivität
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Chemical Information
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Verweise
Calculators
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Biologische Aktivität

Beschreibung

Anwendung

1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.

Chemical Information

CAS. Nr. 1083053-34-2
Unlabeled CAS 103-54-8
Molecular Weight 178.20
Formel C₉¹³C₂H₁₂O₂
SMILES

[13CH3][13C](OC/C=C/C1=CC=CC=C1)=O
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

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

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (273 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[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]

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

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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MOQ

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100 mg

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Cinnamyl acetate-13C2

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Cinnamyl acetate-13C2 Related Classifications

HY-N7125S Related Classifications

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