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trans-Cinnamic acid

trans-Cinnamic acid Structure
CAS No.
140-10-3
Chemical Name:
trans-Cinnamic acid
Synonyms
3-PHENYLACRYLIC ACID;CINNAMIC ACID, TRANS-;3-PHENYL-2-PROPENOIC ACID;(E)-Cinnamic acid;(e)-2-propenoicaci;(E)-3-Phenylacrylic acid;TRANS-3-PHENYLACRYLIC ACID;trans-Cinnamicacid 140-10-3;(2E)-3-phenylprop-2-enoic acid;2-Propenoic acid, 3-phenyl-, (E)-
CBNumber:
CB7345386
Molecular Formula:
C9H8O2
Molecular Weight:
148.16
MOL File:
140-10-3.mol
MSDS File:
SDS
Modify Date:
2024/6/18 13:26:42

trans-Cinnamic acid Properties

Melting point 133 °C (lit.)
Boiling point 300 °C(lit.)
Density 1.248
vapor pressure 1.3 hPa (128 °C)
refractive index 1.5049 (estimate)
Flash point >230 °F
storage temp. 2-8°C
solubility 0.4g/l
form Crystalline Powder
pka 4.44(at 25℃)
color White to almost white
Specific Gravity 0.91
Odor Faint odour
PH Range 3 - 4
PH 3-4 (0.4g/l, H2O, 20℃)
Odor Type balsamic
Water Solubility 0.4 g/L (20 ºC)
λmax 273nm(MeOH)(lit.)
Merck 14,2299
BRN 1905952
Stability Light Sensitive
InChIKey WBYWAXJHAXSJNI-VOTSOKGWSA-N
LogP 2.130
CAS DataBase Reference 140-10-3(CAS DataBase Reference)
NIST Chemistry Reference Cinnamic acid(140-10-3)
EPA Substance Registry System (E)-Cinnamic acid (140-10-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P305+P351+P338-P261-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  1
RTECS  GD7850000
TSCA  Yes
HS Code  29163900
Toxicity LD50 orally in Rabbit: 2500 mg/kg LD50 dermal Rabbit > 5000 mg/kg
NFPA 704
1
2 0

trans-Cinnamic acid price More Price(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W228826 trans-Cinnamic acid natural, ≥99%, FCC, FG 140-10-3 1SAMPLE-K ₹5347.55 2022-06-14 Buy
Sigma-Aldrich(India) W228826 trans-Cinnamic acid natural, ≥99%, FCC, FG 140-10-3 25G ₹7891.43 2022-06-14 Buy
Sigma-Aldrich(India) W228826 trans-Cinnamic acid natural, ≥99%, FCC, FG 140-10-3 100G ₹16767.93 2022-06-14 Buy
Sigma-Aldrich(India) W228826 trans-Cinnamic acid natural, ≥99%, FCC, FG 140-10-3 1KG ₹68738.75 2022-06-14 Buy
Sigma-Aldrich(India) W228818 trans-Cinnamic acid ≥99%, FG 140-10-3 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Product number Packaging Price Buy
W228826 1SAMPLE-K ₹5347.55 Buy
W228826 25G ₹7891.43 Buy
W228826 100G ₹16767.93 Buy
W228826 1KG ₹68738.75 Buy
W228818 1SAMPLE-K ₹5141.88 Buy

trans-Cinnamic acid Chemical Properties,Uses,Production

Chemical Properties

White to almost white crystalline powder. Insoluble in water, slightly soluble in hot water, easily soluble in benzene, acetone, ether, glacial acetic acid and other organic solvents.

Uses

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.

Definition

ChEBI: Cinnamic acid is a monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. It is found in Cinnamomum cassia. It has a role as a plant metabolite. It is a member of styrenes and a member of cinnamic acids. It is a conjugate acid of a cinnamate.

General Description

trans-Cinnamic acid is an α,β-unsaturated aromatic acid that can be used as a flavoring agent. It is mainly used to prepare ester derivatives that are used in perfume industry. trans-Cinnamic acid is the key volatile components of cinnamon essential oil.

Purification Methods

Crystallise the acid from *benzene, CCl4, hot water, water/EtOH (3:1), or 20% aqueous EtOH. Dry it at 60o in vacuo. It is steam volatile. [Beilstein 9 IV 2002.]

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