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Merck
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Documentos

97013

Supelco

trans-Cinnamic acid

analytical standard

Sinónimos:

(2E)-3-Phenyl-2-propenoic acid, trans-3-Phenylacrylic acid

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About This Item

Fórmula empírica (notación de Hill):
C9H8O2
Número de CAS:
140-10-3
Peso molecular:
148.16
Beilstein:
1905952
Número CE:
205-398-1
Número MDL:
MFCD00004369
Código UNSPSC:
85151701
ID de la sustancia en PubChem:
329770541
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Análisis

≥98.0% (HPLC)

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

mp

133 °C (lit.)
133-137 °C

aplicaciones

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

OC(=O)\C=C\c1ccccc1

InChI

1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+

Clave InChI

WBYWAXJHAXSJNI-VOTSOKGWSA-N

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Descripción general

trans-Cinnamic acid occurs in plants, formed via deamination of L-phenylalanine in the presence of enzymatic catalyst, L-phenylalanine ammonia-lyase.

Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Otras notas

This compound is commonly found in plants of the genus: cinnamomum curcuma

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H319

Clasificaciones de peligro

Eye Irrit. 2

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

320.0 °F - closed cup

Punto de inflamabilidad (°C)

160 °C - closed cup

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCC7148
BCBW2848
BCBR2572V
BCBL5967V
BCBF3046

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Production of L-phenylalanine from trans-cinnamic acid with Rhodotorula glutinis containing L-phenylalanine ammonia-lyase activity.
Yamada S, et al.
Applied and Environmental Microbiology, 42(5), 773-778 (1981)
Salicylic Acid: A Multifaceted Hormone (2017)
Feng Yang et al.
Molecular pharmaceutics, 9(11), 3259-3265 (2012-09-27)
Owing to advantageous biochemical and pharmacological properties of human serum albumin (HSA), HSA-based drug carrier is playing an increasing role in the clinical setting. Since the IIA subdomain of HSA is a big hydrophobic cavity, we proposed that HSA delivers
Andrew M Lauer et al.
Organic letters, 14(19), 5138-5141 (2012-09-25)
A highly regioselective, Pd-catalyzed allylic fluorination of phosphorothioate esters is reported. This chemistry addresses several limitations of previously reported methods in which elimination and lack of reactivity were problematic. Preliminary mechanistic investigations reveal that these reactions are stereospecific and provide
Hee Jin Seo et al.
Journal of nanoscience and nanotechnology, 13(3), 1727-1732 (2013-06-13)
Novel liposomes composed of dioleoylphosphatidylethanolamine (DOPE) and 2-(hexadecyloxy) cinnamic acid (HOCA) were prepared by a detergent removal method. When the molar ratio of DOPE to HOCA was 4:1, 3:2, and 2:3, the florescence quenching degree of 5(6)-carboxylic fluorescein (CF, a
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