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3,5-Diethyl-4-hydroxybenzaldehyde, commonly known as vanillin, is an organic compound with the molecular formula C10H12O3. It is a white to light yellow crystalline powder that exhibits a sweet, creamy, and vanilla-like odor. Vanillin is a versatile compound that is naturally derived from vanilla beans and can also be synthesized from other precursors. It possesses antioxidant and antimicrobial properties and is being studied for its potential health benefits, such as reducing inflammation and improving cholesterol levels.

69574-07-8

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69574-07-8 Usage

Uses

Used in Food and Beverage Industry:
3,5-Diethyl-4-hydroxybenzaldehyde is used as a flavoring agent in the food and beverage industry for its characteristic sweet and vanilla-like aroma. It imparts a pleasant taste and scent to various food products, making it a popular choice for manufacturers.
Used in Perfumery:
In the perfume industry, 3,5-diethyl-4-hydroxybenzaldehyde is used as a fragrance ingredient for its distinctive vanilla scent. It is incorporated into perfumes and other scented products to provide a warm and comforting aroma.
Used in Pharmaceutical Production:
3,5-Diethyl-4-hydroxybenzaldehyde is used in the production of pharmaceuticals due to its antioxidant and antimicrobial properties. It can be incorporated into medications to enhance their effectiveness and provide additional health benefits.
Used in Antioxidant Applications:
As an antioxidant, 3,5-diethyl-4-hydroxybenzaldehyde is used to protect against oxidative stress and damage in various applications. Its ability to neutralize free radicals can help prevent cellular damage and support overall health.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, 3,5-diethyl-4-hydroxybenzaldehyde is used in applications where controlling the growth of microorganisms is essential. It can be incorporated into products such as cleaning agents, sanitizers, and preservatives to maintain cleanliness and prevent the spread of bacteria and other pathogens.
Used in Health and Nutrition Research:
3,5-Diethyl-4-hydroxybenzaldehyde is being studied for its potential health benefits, such as its ability to reduce inflammation and improve cholesterol levels. Researchers are exploring its use in the development of nutraceuticals and dietary supplements to promote overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 69574-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69574-07:
(7*6)+(6*9)+(5*5)+(4*7)+(3*4)+(2*0)+(1*7)=168
168 % 10 = 8
So 69574-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-3-9-5-8(7-12)6-10(4-2)11(9)13/h5-7,13H,3-4H2,1-2H3

69574-07-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Diethyl-4-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3,5-diethyl-4-hydroxy-benzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69574-07-8 SDS

69574-07-8Relevant academic research and scientific papers

Peroxynitrite generation from a NO-releasing nitrobenzene derivative in response to photoirradiation

Ieda, Naoya,Nakagawa, Hidehiko,Horinouchi, Taeko,Peng, Tao,Yang, Dan,Tsumoto, Hiroki,Suzuki, Takayoshi,Fukuhara, Kiyoshi,Miyata, Naoki

, p. 6449 - 6451 (2011/06/27)

Photocontrollable ONOO- generation from a nitrobenzene derivative was demonstrated. The designed compound released NO in response to photoirradiation, and the resulting semiquinone reduced molecular oxygen to generate O2-; reaction of the two generated ONOO -, as confirmed with an ONOO- fluorescent probe, HKGreen-3.

PROCESS FOR THE PREPARATION OF HYDROQUINONES

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Page/Page column 18-19, (2011/11/01)

The invention relates to a process for the preparation of a hydroquinone compound of formula (I) wherein R2, R3, R5 and R6 have the meaning according to claim 1, with the steps of formylating a substituted phenol and oxidising the resulting substituted 4-hydroxy- benzaldehyde under acidic conditions to the corresponding hydroquinone of formula (I). Another object of the invention concerns the intermediate 2,3,5-trimethyl-4-hydroxy- benzaldehyde for synthesis of 2,3,5-trimethyl-hydroquinone (TMHQ) and (dl)cc-tocopherol.

NOVEL THIOPHENE DERIVATIVES

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Page/Page column 73, (2010/02/15)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

HYDROGENATED BENZO (C) THIOPHENE DERIVATIVES AS IMMUNOMODULATORS

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Page/Page column 45, (2010/11/24)

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

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