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40348-72-9

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40348-72-9 Usage

Description

Methyl 2-hydroxy-4-methylvalerate, also known as methyl 2-hydroxy-4-methylpentanoate, is an organic compound with a sweet, fruity, and musty odor. It is found in guanabana and is characterized by its unique chemical properties that contribute to its distinct smell.

Uses

Used in Flavor Industry:
Methyl 2-hydroxy-4-methylvalerate is used as a flavoring agent for its sweet, fruity, and musty odor. It is particularly useful in the creation of artificial fruit flavors, enhancing the taste and aroma of various food and beverage products.
Used in Fragrance Industry:
In the fragrance industry, methyl 2-hydroxy-4-methylvalerate is used as a component in the formulation of perfumes and other scented products. Its sweet, fruity, and musty odor adds depth and complexity to the overall scent, making it a valuable addition to the perfumer's palette.
Used in Cosmetics Industry:
Methyl 2-hydroxy-4-methylvalerate is also utilized in the cosmetics industry, where it serves as a key ingredient in the development of lotions, creams, and other personal care products. Its pleasant odor and chemical properties make it an ideal component for enhancing the sensory experience of these products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, methyl 2-hydroxy-4-methylvalerate may be used as an active ingredient or additive in the development of medications, particularly those targeting respiratory or digestive issues. Its sweet, fruity, and musty odor can help mask unpleasant tastes, making it easier for patients to take their medication.
Overall, methyl 2-hydroxy-4-methylvalerate is a versatile compound with a wide range of applications across various industries, primarily due to its unique and appealing odor.

Check Digit Verification of cas no

The CAS Registry Mumber 40348-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,4 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40348-72:
(7*4)+(6*0)+(5*3)+(4*4)+(3*8)+(2*7)+(1*2)=99
99 % 10 = 9
So 40348-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O3/c1-5(2)4-6(8)7(9)10-3/h5-6,8H,4H2,1-3H3

40348-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-hydroxy-4-methylpentanoate

1.2 Other means of identification

Product number -
Other names Methyl 2-hydroxy-4-methylvalerate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:40348-72-9 SDS

40348-72-9Relevant articles and documents

PROCESS OF PRODUCING ALPHA-HYDROXY COMPOUNDS AND USES THEREOF

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Page/Page column 23; 24, (2019/08/29)

New process of producing alpha-hydroxy compounds from sustainable resources useful as platform chemicals, such as hydroxy analogues of amino acids or polymer precursors.

Catalytic asymmetric glyoxylate-ene reaction: A practical access to α-hydroxy esters in high enantiomeric purities

Mikami, Koichi,Terada, Masahiro,Nakai, Takeshi

, p. 3949 - 3954 (2007/10/02)

An efficient asymmetric catalysis is developed for the glyoxylate-ene reaction to afford the α-hydroxy esters of biological and synthetic importance. The key to the success is the use of the chiral titanium complex prepared in situ from (i-PrO)2TiX2 (X = Cl or Br) and the (R)- or (S)-binaphthol in the presence of molecular sieves (MS 4A). The presence of the molecular sieves (zeolite) is clarified to facilitate the alkoxy-ligand exchange reaction. Thus, the use of MS is shown to be essential for the in situ preparation step of the chiral catalyst and not for the ene reaction step. The present catalytic process is applicable to various 1,1-disubstituted olefins by the judicious choice of the dichloro or dibromo catalyst.

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