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29006-01-7

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  • 29006-01-7 Structure

  • Basic information

    1. Product Name: Methyl 4-methoxybutanoate
    2. Synonyms: 4-Methoxybutyric acid methyl ester;4-Methoxybutanoic acid methyl ester;Methyl 4-methoxybutyrate 98%;Butanoic acid, 4-methoxy-, methyl ester;Butyric acid, 4-methoxy-, methyl ester;methl,4-methoxybutyrate;METHYL 4-METHOXYBUTYRATE;METHYL 4-METHOXYBUTANOATE
    3. CAS NO:29006-01-7
    4. Molecular Formula: C6H12O3
    5. Molecular Weight: 132.16
    6. EINECS: N/A
    7. Product Categories: C6 to C7;Carbonyl Compounds;Esters
    8. Mol File: 29006-01-7.mol
    9. Article Data: 2

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 162-164 °C767 mm Hg(lit.)
    3. Flash Point: 130 °F
    4. Appearance: /
    5. Density: 0.969 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 3.1mmHg at 25°C
    7. Refractive Index: n20/D 1.408(lit.)
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: Methyl 4-methoxybutanoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl 4-methoxybutanoate(29006-01-7)
    12. EPA Substance Registry System: Methyl 4-methoxybutanoate(29006-01-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 10
    3. Safety Statements: 16
    4. RIDADR: UN 3272 3/PG 3
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 29006-01-7(Hazardous Substances Data)

29006-01-7 Usage

Description

Methyl 4-methoxybutanoate, an organic compound with the chemical formula C6H12O3, is a colorless liquid characterized by a fruity odor. It is recognized for its stability, low volatility, and low toxicity, which contribute to its safety in a variety of consumer applications.

Uses

Used in Flavoring Industry:
Methyl 4-methoxybutanoate is used as a flavoring agent for its distinctive fruity scent, enhancing the taste and aroma profiles of food and beverages.
Used in Industrial Processes:
In various industries, Methyl 4-methoxybutanoate serves as a solvent, facilitating numerous processes due to its ability to dissolve a wide range of substances.
Used in Pharmaceutical Synthesis:
Methyl 4-methoxybutanoate is utilized as an intermediate in the synthesis of pharmaceuticals, playing a crucial role in the production of various medicinal compounds.
Used in Organic Compound Synthesis:
Methyl 4-methoxybutanoate is also employed in the synthesis of other organic compounds, highlighting its versatility in chemical reactions and its importance in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 29006-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29006-01:
(7*2)+(6*9)+(5*0)+(4*0)+(3*6)+(2*0)+(1*1)=87
87 % 10 = 7
So 29006-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O3/c1-8-5-3-4-6(7)9-2/h3-5H2,1-2H3

29006-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-methoxybutanoate

1.2 Other means of identification

Product number -
Other names 4-Methoxy-buttersaeure-methylester

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:29006-01-7 SDS

29006-01-7Relevant articles and documents

Upgrading biomass-derived furans via acid-catalysis/hydrogenation: The remarkable difference between water and methanol as the solvent

Hu, Xun,Westerhof, Roel J. M.,Wu, Liping,Dong, Dehua,Li, Chun-Zhu

, p. 219 - 224 (2018/04/16)

In methanol 5-hydroxymethylfurfural (HMF) and furfuryl alcohol (FA) can be selectively converted into methyl levulinate via acidcatalysis, whereas in water polymerization dominates. The hydrogenation of HMF, furan and furfural with the exception of FA is

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