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trans-Cinnamic acid, 99+%
CAS: 140-10-3 | C9H8O2 | 148.161 g/mol
$61.01 - $694.38
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 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1353822
|
Thermo Scientific Chemicals
A1353822 |
100 g |
Each for $61.01
|
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|
AAA1353836
|
Thermo Scientific Chemicals
A1353836 |
500 g |
Each for $178.96
|
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|
AAA135380E
|
Thermo Scientific Chemicals
A135380E |
2500 g |
Each for $694.38
|
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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.
Applicationstrans-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.
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
| 133°C to 136°C | |
| 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 | |
| 166°C (330°F) |
| 140-10-3 | |
| ≥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% | |
| 100 g | |
| trans-Cinnamic Acid |
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
EINECSNumber : 205-398-1
RTECSNumber : GD7850000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only