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112372

Sigma-Aldrich

Ethyl cinnamate

99%

Synonyme(s) :

3-Phenyl-2-propenoic acid ethyl ester, Ethyl 3-phenyl-2-propenoate, NSC 6773

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About This Item

Formule linéaire :
C6H5CH=CHCOOC2H5
Numéro CAS:
103-36-6
Poids moléculaire :
176.21
Numéro Beilstein :
775541
Numéro CE :
203-104-6
Numéro MDL:
MFCD00009189
Code UNSPSC :
12352100
ID de substance PubChem :
24847091
Nomenclature NACRES :
NA.22

Pureté

99%

Impuretés

may contain alpha-tocopherol (synthetic)

Indice de réfraction

n20/D 1.558 (lit.)

Point d'ébullition

271 °C (lit.)

Pf

6-8 °C (lit.)

Densité

1.049 g/mL at 20 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

CCOC(=O)\C=C\c1ccccc1

InChI

1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+

Clé InChI

KBEBGUQPQBELIU-CMDGGOBGSA-N

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Application

  • Antimicrobial and antiproliferative effects: Essential oils including Ethyl cinnamate derived from Zingiberaceae family show promising antimicrobial and antiproliferative properties, suggesting their potential application in oral healthcare products. This study provides insight into the utilization of natural products for medical and pharmaceutical applications (Amil et al., 2024).
  • Biodistribution and cellular interactions in medical research: Ethyl cinnamate could be investigated for its role in enhancing the permeability and imaging contrast in studies like those investigating the biodistribution of intravenously delivered mesenchymal stromal cells. Such applications could improve understanding in cellular therapies and regenerative medicine (Pichardo et al., 2022).

Actions biochimiques/physiologiques

Ethyl cinnamate inhibits the growth of Chlorella pyrenoidosa.

Autres remarques

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Gessica D Gonçalves et al.
Anatomical record (Hoboken, N.J. : 2007), 303(10), 2668-2678 (2020-01-28)
Fetal hypoxia is a common complication of pregnancy. We have previously reported that maternal hypoxia in late gestation in mice gives rise to male offspring with reduced nephron number, while females have normal nephron number. Male offspring later develop proteinuria
Li-Li Gao et al.
Huan jing ke xue= Huanjing kexue, 34(1), 156-162 (2013-03-16)
The effects of ethyl cinnamate on the growth and physiological characteristics of Chlorella pyrenoidosa were studied. The allelopathic mechanisms were explored, from views of chlorophyll a content, antioxidant enzyme activities, reactive oxygen species (ROS) level, malondialdehyde (MDA) content and photosynthetic
Linfang Huang et al.
Journal of ethnopharmacology, 120(1), 123-125 (2008-09-02)
It is well known that fragrance impacts behaviors and autonomic functions, and is increasingly used as relaxant, carminative, as well as sedative in aromatherapy. Kaempferia galanga L. is one of the popular traditional aromatic medicinal plants used in tropics and
Rozana Othman et al.
Planta medica, 68(7), 655-657 (2002-07-27)
From the rhizomes of Kaempferia galanga, ethyl cinnamate (EC) was isolated and its vasorelaxant effect was examined on the rat aorta. EC inhibited the tonic contractions induced by high K+ and phenylephrine (PE) in a concentration-dependent manner, with respective IC50
Nam-Jin Kim et al.
Pest management science, 64(8), 857-862 (2008-03-08)
This study was aimed at assessing the toxicity of ethyl cinnamate and ethyl p-methoxycinnamate (EMC) identified in Kaempferia galangal L. (Zingiberaceae) rhizome and another 12 known compounds to third-instar larvae from laboratory-reared Culex pipiens pallens Forskal, Aedes aegypti L. and
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