ChemicalBook > Product Catalog >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >cyclitols >Cinnamyl alcohol

Cinnamyl alcohol

Cinnamyl alcohol Structure
CAS No.
104-54-1
Chemical Name:
Cinnamyl alcohol
Synonyms
CINNAMIC ALCOHOL;3-PHENYL-2-PROPEN-1-OL;Sterone;3-phenylprop-2-en-1-ol;TRANS-CINNAMYL ALCOHOL;(E)-3-phenyl-2-propen-1-ol;Cinnamylalkohol;3-PHENYLPROPENOL;(2E)-3-Phenyl-2-propen-1-ol;stylone
CBNumber:
CB5771763
Molecular Formula:
C9H10O
Molecular Weight:
134.18
MOL File:
104-54-1.mol
MSDS File:
SDS
Modify Date:
2025/1/27 9:38:02

Cinnamyl alcohol Properties

Melting point 30-33 °C (lit.)
Boiling point 250 °C (lit.)
Density 1.044 g/mL at 25 °C (lit.)
vapor density 4.6 (vs air)
vapor pressure <0.01 mm Hg ( 25 °C)
FEMA 2294 | CINNAMYL ALCOHOL
refractive index 1.5819
Flash point >230 °F
storage temp. -20°C
solubility H2O: soluble
form Fused Low Melting Crystalline Solid
pka 0.852[at 20 ℃]
Specific Gravity 1.044
color White
Odor at 100.00 %. sweet balsam hyacinth spicy green powdery cinnamic
Odor Type balsamic
biological source synthetic
Water Solubility 1.8 g/L (20 ºC)
Merck 14,2302
JECFA Number 647
BRN 1903999
Stability Stable. Incompatible with strong oxidizing agents.
InChIKey OOCCDEMITAIZTP-QPJJXVBHSA-N
LogP 1.452 at 25℃
CAS DataBase Reference 104-54-1(CAS DataBase Reference)
NIST Chemistry Reference 2-Propen-1-ol, 3-phenyl-(104-54-1)
EPA Substance Registry System 3-Phenyl-2-propen-1-ol (104-54-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H317-H411
Precautionary statements  P261-P264-P273-P280-P301+P312-P302+P352
Hazard Codes  Xn
Risk Statements  22-36/38-43-36
Safety Statements  26-36/37-37/39-24-24/25
RIDADR  2811
WGK Germany  2
RTECS  GE2200000
10-23
TSCA  Yes
HS Code  29062990
Hazardous Substances Data 104-54-1(Hazardous Substances Data)
Toxicity LD50 (g/kg): 2.0 orally in rats; >5.0 dermally in rabbits (Letizia)
NFPA 704
1
2 0

Cinnamyl alcohol price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W229407 Cinnamyl alcohol ≥98%, FG 104-54-1 1SAMPLE-K ₹4990.33 2022-06-14 Buy
Sigma-Aldrich(India) W229407 Cinnamyl alcohol ≥98%, FG 104-54-1 1KG ₹8389.38 2022-06-14 Buy
Sigma-Aldrich(India) W229407 Cinnamyl alcohol ≥98%, FG 104-54-1 5KG ₹26088.25 2022-06-14 Buy
Sigma-Aldrich(India) W229407 Cinnamyl alcohol ≥98%, FG 104-54-1 10KG ₹33341 2022-06-14 Buy
Sigma-Aldrich(India) W229407 Cinnamyl alcohol ≥98%, FG 104-54-1 25KG ₹60219.48 2022-06-14 Buy
Product number Packaging Price Buy
W229407 1SAMPLE-K ₹4990.33 Buy
W229407 1KG ₹8389.38 Buy
W229407 5KG ₹26088.25 Buy
W229407 10KG ₹33341 Buy
W229407 25KG ₹60219.48 Buy

Cinnamyl alcohol Chemical Properties,Uses,Production

Description

Occupational cases of contact dermatitis were reported in the perfurne industry. Patch tests can also be positive in food handlers. Cinnamic alcohol is contained in the "fragrance mix".

Chemical Properties

Cinnamyl alcohol can exist in (Z)-[4510-34-3] and (E)-[4407-36-7] forms. Although both isomers occur in nature, the (E)-isomer is far more abundant and is present, for example, in styrax oil. (E)-Cinnamyl alcohol is a colorless, crystalline solid with a hyacinth-like balsamic odor.
Cinnamyl alcohol can be dehydrogenated to give cinnamaldehyde and oxidized to give cinnamic acid. Hydrogenation yields 3-phenylpropanol and/or 3-cyclohexylpropanol. Reaction with carboxylic acids or carboxylic acid derivatives results in the formation of cinnamyl esters, some of which are used as fragrance materials.

Occurrence

Occurring as an ester or in the free state in hyacinth, Aristolochia clematis, Xanthorrhoea hastilis and in the essence of daffodil flowers. It is also reported found in guava fruit and peel, lemon peel oil, cassia leaf, Bourbon vanilla and cinnamon bark, leaf and root.

Uses

Cinnamyl alcohol was used to study the alkylation of 2,4-di-tert-butylphenol by cinnamyl alcohol using aluminum-containing mesoporous ethane-silica catalyst. It was used to study gold nanoparticles supported on titanium dioxide catalysed oxidative coupling of alcohols and amines to form the corresponding imines.

Preparation

By reduction of cinnamic aldehyde.

Definition

ChEBI: A primary alcohol comprising an allyl core with a hydroxy substituent at the 1-position and a phenyl substituent at the 3-position (geometry of the C2C bond unspecified).

Contact allergens

Cinnamyl alcohol occurs (in esterified form) in storax, Myroxylon pereirae, cinnamon leaves, and hyacinth oil. It is obtained by the alkaline hydrolysis of storax and prepared synthetically by reducing cinnamal diacetate with iron filings and acetic acid, and from cinnamaldehyde by Meerwein-Ponndorf reduction with aluminum isopropoxide. Cinnamyl alcohol is contained in the “fragrance mix.” As a fragrance allergen, it has to be mentioned by name in cosmetics within the EU. Occupational cases of contact dermatitis were reported in perfume industry. Patch tests can be positive in food handlers.

Purification Methods

Crystallise the alcohol from diethyl ether/pentane. [Beilstein 6 I 281.]

Global( 730)Suppliers
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