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Postion:Product Catalog >Organic Chemistry>Alcohols,Phenols,Phenol alcohols>cyclitols>Cinnamyl alcohol
Cinnamyl alcohol
  • Cinnamyl alcohol

Cinnamyl alcohol

Price $1
Package 1kg
Min. Order: 1kg
Supply Ability: 100KG
Update Time: 2019-07-06

Product Details

Product Name: Cinnamyl alcohol CAS No.: 104-54-1
Min. Order: 1kg Purity: 99%
Supply Ability: 100KG Release date: 2019/07/06

AD68

Cinnamyl alcohol Basic information
Description References
Product Name: Cinnamyl alcohol
Synonyms: (2E)-3-Phenyl-2-propen-1-ol;1-Phenyl-1-propen-3-ol;2-Propen-1-ol,3-phenyl-;3-Fenyl-2-propen-1-ol;3-phenyl-2-propen-1-o;3-Phenyl-2-propenol;3-phenyl-prop-2-en-1-ol;3-phenylprop-2-en-1-ol
CAS: 104-54-1
MF: C9H10O
MW: 134.18
EINECS: 203-212-3
Product Categories: Pharmaceutical Intermediates;Benzhydrols, Benzyl & Special Alcohols;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Cosmetics
Mol File: 104-54-1.mol
Article illustration
 
Cinnamyl alcohol Chemical 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)
refractive index  1.5819
FEMA  2294 | CINNAMYL ALCOHOL
Fp  >230 °F
storage temp.  2-8°C
solubility  H2O: soluble
form  Fused Low Melting Crystalline Solid
color  White
Water Solubility  1.8 g/L (20 ºC)
Merck  14,2302
BRN  1903999
Stability: Stable. Incompatible with strong oxidizing agents.
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 2-Propen-1-ol, 3-phenyl-(104-54-1)
 
Safety Information
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
Hazardous Substances Data 104-54-1(Hazardous Substances Data)
Toxicity LD50 (g/kg): 2.0 orally in rats; >5.0 dermally in rabbits (Letizia)
MSDS Information
Provider Language
3-Phenyl-2-propene-1-ol English
ACROS English
SigmaAldrich English
ALFA English
 
Cinnamyl alcohol Usage And Synthesis
Description As an organic compound, Cinnamic alcohol has a very distinct sweet, spicy, hyacinth odour that is found in resins, balsams and cinnamon leaves. It is used commonly in the fragrance industry due to its distinctive odour, which can be applied as a deodorant, fragrance and additive in cosmetic products and in the formulation of bath products, body and hand products, such as soaps, toothpaste, deodorants, etc. Besides, it also finds application as a food additive in chewing gum, bakery products, candy and soft drinks. Naturally, Cinnamyl alcohol is occurrent only in small amount, thus its industrial demand is usually fulfilled by chemical synthesis starting from the reduction of cinnamaldehyde.
Cinnamyl alcohol has been found to have a sensitising effect on some particular people, thus it is also considered as a Standardized Chemical Allergen. The physiologic effect of cinnamyl alcohol is caused by the Increased Histamine Release and cell-mediated Immunity.
References https://en.wikipedia.org/wiki/Cinnamyl_alcohol
http://www.huidziekten.nl/allergie/stoffen/cinnamic-alcohol.htm
https://www.ulprospector.com/en/na/Food/Detail/13286/411638/Cinnamic-Alcohol
http://www.cosmeticsinfo.org/ingredient/cinnamyl-alcohol-0
https://pubchem.ncbi.nlm.nih.gov/compound/cinnamyl_alcohol#section=Top
http://www.somaiya.com/products/chemicals-pipeline/cinnamic-alcohol-1
Chemical Properties colourless solid
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.
Uses cinnamyl alcohol is naturally occurring in cinnamon bark, it can also be synthetically manufactured. It is used in cosmetics as a fragrance or flavoring agent.
Uses In perfumery; as deodorant in 12.5% solution in glycerol.
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. Cinnamic 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.]
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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