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trans-Cinnamic acid, 99+%, Thermo Scientific Chemicals

27.20 € - 306.00 €

Chemical Identifiers

CAS 140-10-3
Molecular Formula C9H8O2
Molecular Weight (g/mol) 148.161
MDL Number MFCD00004369
InChI Key WBYWAXJHAXSJNI-VOTSOKGWSA-N
Synonym cinnamic acid, trans-cinnamic acid, e-cinnamic acid, 3-phenylacrylic acid, trans-3-phenylacrylic acid, zimtsaeure, 2e-3-phenylprop-2-enoic acid, 3-phenylprop-2-enoic acid, 3-phenylpropenoic acid
PubChem CID 444539
ChEBI CHEBI:35697
IUPAC Name (E)-3-phenylprop-2-enoic acid
SMILES C1=CC=C(C=C1)C=CC(=O)O
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Products 3
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Product Code Brand Quantity Price Quantity & Availability  
11480004
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Thermo Scientific Alfa Aesar
A13538.22
100 g
27.20 €
100g
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11490004
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Thermo Scientific Alfa Aesar
A13538.36
500 g
70.50 €
500g
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11400014
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Thermo Scientific Alfa Aesar
A13538.0E
2500 g
306.00 €
2500g
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Description

Description

trans-Cinnamic acid is used in flavors, synthetic indigo and pharmaceuticals. It is involved in the production of methyl, ethyl and benzyl esters, which is used in the perfume industry. It serves as a precursor to the sweetener aspartame through enzyme-catalyzed amination to phenylalanine. It is a self-inhibitor produced by fungal spores to prevent germination. In addition, it is used to establish phenolic compounds by liquid chromatography, ultraviolet and mass spectrometry. It is utilized as a potential agent, thereby preventing lung tumor cells from metastasizing. Further, it induces intracellular release of calcium ions from the vacuole to the cytoplasm in order to trigger phytotoxicity in cucumber.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
trans-Cinnamic acid is used in flavors, synthetic indigo and pharmaceuticals. It is involved in the production of methyl, ethyl and benzyl esters, which is used in the perfume industry. It serves as a precursor to the sweetener aspartame through enzyme-catalyzed amination to phenylalanine. It is a self-inhibitor produced by fungal spores to prevent germination. In addition, it is used to establish phenolic compounds by liquid chromatography, ultraviolet and mass spectrometry. It is utilized as a potential agent, thereby preventing lung tumor cells from metastasizing. Further, it induces intracellular release of calcium ions from the vacuole to the cytoplasm in order to trigger phytotoxicity in cucumber.

Solubility
Soluble in many organic solvents. Slightly soluble in water.

Notes
Incompatible with strong oxidizing agents.
Specifications

Chemical Identifiers

140-10-3
148.161
WBYWAXJHAXSJNI-VOTSOKGWSA-N
444539
(E)-3-phenylprop-2-enoic acid
C9H8O2
MFCD00004369
cinnamic acid, trans-cinnamic acid, e-cinnamic acid, 3-phenylacrylic acid, trans-3-phenylacrylic acid, zimtsaeure, 2e-3-phenylprop-2-enoic acid, 3-phenylprop-2-enoic acid, 3-phenylpropenoic acid
CHEBI:35697
C1=CC=C(C=C1)C=CC(=O)O

Specifications

140-10-3
147°C (4 mm)
C9H8O2
1905952
cinnamic acid, trans-cinnamic acid, e-cinnamic acid, 3-phenylacrylic acid, trans-3-phenylacrylic acid, zimtsaeure, 2e-3-phenylprop-2-enoic acid, 3-phenylprop-2-enoic acid, 3-phenylpropenoic acid
WBYWAXJHAXSJNI-VOTSOKGWSA-N
(E)-3-phenylprop-2-enoic acid
444539
148.16
0.910
trans-Cinnamic Acid
133°C to 136°C
≥99%
MFCD00004369
14,2299
Soluble in many organic solvents. Slightly soluble in water.
C1=CC=C(C=C1)C=CC(=O)O
148.161
CHEBI:35697
≥99%
166°C (330°F)
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

missing translation for 'einecsNumber' : 205-398-1

missing translation for 'rtecsNumber' : GD7850000

missing translation for 'tsca' : Yes

Recommended Storage : Ambient temperatures

SDS
Documents

Documents

Product Certifications

RUO – Research Use Only