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3-Phenylpropionaldehyde(CAS#104-53-0)

Chemical Property:

Molecular Formula C9H10O
Molar Mass 134.18
Density 1.019 g/mL at 25 °C (lit.)
Melting Point -42 °C
Boling Point 97-98 °C/12 mmHg (lit.)
Flash Point 203°F
JECFA Number 645
Water Solubility Miscible with chloroform, dichloromethane, ethyl acetate, alcohol and ether. Immiscible with water.
Solubility 0.74mg/l
Vapor Presure 15 hPa (98 °C)
Appearance Liquid
Color Clear colorless to light yellow
BRN 1071910
Storage Condition Store below +30°C.
Sensitive Air Sensitive
Refractive Index n20/D 1.523(lit.)
Physical and Chemical Properties Colorless liquid. There is a fragrance like the Hyacinth. Density 1.010-1.020. Melting point 47. Boiling Point 221-224 °c (0.1 MPa, 744 Hg). Refractive index 532. Soluble in ethanol.
Use Widely used in the preparation of a variety of floral essences, especially clove, jasmine and rose flavor

Product Detail

Product Tags

Hazard Symbols Xi – Irritant
Risk Codes R36/38 – Irritating to eyes and skin.
R36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 – Wear suitable protective clothing.
S37/39 – Wear suitable gloves and eye/face protection
WGK Germany 2
RTECS MW4890000
FLUKA BRAND F CODES 10-23
TSCA Yes
HS Code 29122900
Toxicity LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 5000 mg/kg

 

Introduction

Phenylpropionaldehyde, also known as benzylforme. The following is an introduction to the properties, uses, preparation methods and safety information of phenylpropionaldehyde:

 

1. Nature:

- Appearance: Phenylpropional is a colorless liquid that can sometimes be yellow.

- Smell: with a special aromatic aroma.

- Density: relatively high.

- Solubility: Soluble in many organic solvents, including alcohols and ethers.

 

2. Usage:

- Chemical synthesis: Phenylpropionaldehyde is one of the important raw materials for many organic synthesis, which can be used to prepare a variety of organic compounds.

 

3. Method:

- Acetic anhydride method: Phenylpropanol is reacted with acetic anhydride under acid-catalyzed conditions to produce phenylpropylacetic anhydride, which is then devinegared to benzyl acetic acid, and finally converted to phenylpropional by oxidation.

- Response mechanism method: Phenylpropyl bromide is reacted with a mixture of sodium cyanide and sodium hydroxide to generate phenylpropionazone, which is then hydrolyzed by heating to obtain benzylamine, and finally oxidized to phenylpropionaldehyde.

 

4. Safety Information:

- Phenylpropional is irritating and corrosive, contact with skin and eyes should be avoided, and protective gloves and goggles should be worn if necessary.

- During use and storage, attention should be paid to the risk of fire prevention and static build-up.

- Phenylpropionaldehyde may cause harm to the environment, and appropriate environmental protection measures should be taken to deal with it when it leaks.


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