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4,4-Diethoxybutan-1-ol, also known as DEB, is a colorless liquid chemical compound with the molecular formula C8H18O3. It has a mild, floral odor and is primarily used as a solvent in various industrial applications. DEB is also utilized as a flavor and fragrance ingredient, as well as in the production of pharmaceuticals and other chemicals. This versatile compound possesses properties that make it suitable for a wide range of applications and is considered relatively safe when handled and used properly.

70216-75-0

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70216-75-0 Usage

Uses

Used in Solvent Applications:
4,4-Diethoxybutan-1-ol is used as a solvent in various industries for its ability to dissolve a wide range of substances, making it a valuable component in the formulation of products such as paints, coatings, and adhesives.
Used in Flavor and Fragrance Industry:
DEB is used as a flavor and fragrance ingredient due to its mild, floral odor, contributing to the creation of various scents and flavors in products like perfumes, cosmetics, and food items.
Used in Pharmaceutical Production:
4,4-Diethoxybutan-1-ol is utilized in the production of pharmaceuticals, where it serves as a key component in the synthesis of various medications, highlighting its importance in the development of new drugs.
Used in Chemical Production:
DEB is employed in the production of other chemicals, showcasing its versatility and applicability in the chemical industry for creating a diverse range of products.

Check Digit Verification of cas no

The CAS Registry Mumber 70216-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,1 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70216-75:
(7*7)+(6*0)+(5*2)+(4*1)+(3*6)+(2*7)+(1*5)=100
100 % 10 = 0
So 70216-75-0 is a valid CAS Registry Number.

70216-75-0Downstream Products

70216-75-0Relevant academic research and scientific papers

Catalytic asymmetric transacetalization

Coric, Ilija,Vellalath, Sreekumar,List, Benjamin

supporting information; experimental part, p. 8536 - 8537 (2010/08/06)

A catalytic enantioselective transacetalization has been developed. The chiral phosphoric acid TRIP was demonstrated to be an efficient and highly enantioselective catalyst for the activation of O, O-acetals. The reaction enables the asymmetric synthesis of acetals with the acetal carbon as the only stereogenic center.

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