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13327-56-5

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  • Ethyl 3-methylthiopropionate Safe Shipping 99% RARECHEM AL BI 0161 Reached Safely ETHYL-BETA-METHYLTHIOPROPIONATE Powder Ethyl 3-methylthio propionate Raw Material

    Cas No: 13327-56-5

  • USD $ 1.32-1.32 / Gram

  • 10 Gram

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13327-56-5 Usage

Description

Ethyl 3-methylthiopropionate is a carboxylic ester that is obtained by the formal condensation of the carboxy group of 3-(methylthio)propionic acid with ethanol. It is a clear colorless to pale yellowish liquid with a pineapple, citrus odor and fruity, pineapple, passion fruit, malt whiskey flavor. It has a taste threshold value of 30 ppm and is characterized by a sulfuraceous, onion garlic, fruity, ripe, pulpy, and tomato taste. Ethyl 3-methylthiopropionate is also known to have a detection aroma threshold value of 7 ppb and is described as having a fruity, tinny pineapple, onion sulfurous, musty tomato aroma with metallic ripe and canned notes, savory green with hints of horseradish, and tropical notes.

Uses

Used in Flavor and Fragrance Industry:
Ethyl 3-methylthiopropionate is used as a flavoring agent for its fruity, pineapple, passion fruit, and malt whiskey flavor. Its aroma characteristics make it suitable for use in creating various fragrances and scents.
Used in Food Industry:
Ethyl 3-methylthiopropionate is used as a flavor enhancer in the food industry to impart a pineapple, citrus, and fruity taste to various food products. Its sulfuraceous, onion garlic, ripe, pulpy, and tomato taste characteristics can also be utilized to enhance the flavor profiles of different dishes.
Used in Beverage Industry:
Ethyl 3-methylthiopropionate is used in the beverage industry to add a unique flavor and aroma to alcoholic and non-alcoholic drinks. Its presence has been reported in beer, grape brandy, cognac, malt whiskey, and wine, where it contributes to the overall taste and aroma of these beverages.
Used in Aromatherapy:
Ethyl 3-methylthiopropionate can be used in aromatherapy for its pleasant and invigorating aroma. Its fruity, pineapple, passion fruit, and malt whiskey scent can help create a relaxing and uplifting atmosphere.
Used in Cosmetics and Personal Care Products:
Ethyl 3-methylthiopropionate can be used in cosmetics and personal care products for its pleasant aroma and flavor. It can be incorporated into perfumes, body lotions, and other personal care products to provide a unique and refreshing scent.
Used in Pharmaceutical Industry:
Ethyl 3-methylthiopropionate can be used in the pharmaceutical industry for its potential therapeutic properties. Its sulfur-containing compounds may have potential applications in the development of new drugs and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 13327-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,2 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13327-56:
(7*1)+(6*3)+(5*3)+(4*2)+(3*7)+(2*5)+(1*6)=85
85 % 10 = 5
So 13327-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2S/c1-3-8-6(7)4-5-9-2/h3-5H2,1-2H3

13327-56-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A11742)  Ethyl 3-(methylthio)propionate, 98%   

  • 13327-56-5

  • 25g

  • 533.0CNY

  • Detail
  • Alfa Aesar

  • (A11742)  Ethyl 3-(methylthio)propionate, 98%   

  • 13327-56-5

  • 100g

  • 953.0CNY

  • Detail
  • Alfa Aesar

  • (A11742)  Ethyl 3-(methylthio)propionate, 98%   

  • 13327-56-5

  • 500g

  • 4037.0CNY

  • Detail

13327-56-5Relevant articles and documents

REACTIONS OF α-HETEROATOM-SUBSTITUTED ETHERS AND SULFIDES WITH SILYL ENOL ETHERS. CHEMOSELECTIVITY IN THE CLEAVAGE OF HETEROATOM-CARBON BONDS BY IODOTRIMETHYLSILANE AND TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE

Hosomi, Akira,Sakata, Yasuyuki,Sakurai, Hideki

, p. 405 - 408 (2007/10/02)

Reactions of α-heteroatom substituted ethers and related compounds (R1R2CXY; X, Y = RO, RS and Cl) with silyl enol ethers and ketene silyl acetals took place in the presence of iodotrimethylsilane (Ia) and trimethylsilyl triflate (Ib) as a catalyst and factors influencing the activation of the heteroatom by I were examined.

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