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68298-29-3

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68298-29-3 Usage

General Description

"(3-methylbutoxy)acetic acid" is a chemical compound with the molecular formula C8H16O3. It is a carboxylic acid with a butoxy group attached to the third carbon atom of the acetic acid molecule. This chemical is commonly used as a solvent and in the production of various products such as esters, perfumes, and pharmaceuticals. It is a clear, colorless liquid with a faint, fruity odor. (3-methylbutoxy)acetic acid is also known by other names including MBOAA and 2-(butoxymethyl)propanoic acid. It is important to handle this chemical with care and to follow safety regulations when using it due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 68298-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,9 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68298-29:
(7*6)+(6*8)+(5*2)+(4*9)+(3*8)+(2*2)+(1*9)=173
173 % 10 = 3
So 68298-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O3/c1-6(2)3-4-10-5-7(8)9/h6H,3-5H2,1-2H3,(H,8,9)

68298-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methylbutoxy)acetic acid

1.2 Other means of identification

Product number -
Other names Isopentyloxy-essigsaeure

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:68298-29-3 SDS

68298-29-3Relevant articles and documents

Synthetic method of propylene isopentoxy acetate perfume

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Paragraph 0027; 0029-0030; 0034; 0036-0037; 0041; 0043-0044, (2019/12/11)

The invention discloses a synthetic method of propylene isopentoxy acetate perfume. According to the invention, a Williamson reaction is replaced, and ethyl diazoacetate and isoamyl alcohol are subjected to an O-H insertion reaction under the catalytic action of the catalyst Rh2(OAc)4 to synthesize propylene isopentoxy acetate, so reaction time is greatly shortened; in addition, the prepared solidacid catalyst Yb-MoO3/Al2O3-ZrO2 has the advantages easy separation from a liquid-phase reaction system, no corrosion to equipment and simple aftertreatment, overcomes the problems that conventionalliquid acid corrodes equipment and acid-containing wastewater pollutes environment, and also has high selectivity; the synthetic method can be carried out at low temperature, reduces energy consumption and side reactions, and greatly improves production efficiency; the yield of the prepared propylene isopentoxy acetate perfume is as high as 98.4%; the propylene isopentoxy acetate perfume has goodheat stability, small possibility of loss of active components and good repeated use performance, and is a novel green catalytic material with great application potential.

Diaminopyrimidine derivatives as growth hormone secrectgogue receptor (GHS-R) antagonists

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Page/Page column 33, (2010/02/13)

The present invention is related to compounds of formula (I), or a therapeutically suitable salt or prodrug thereof, the preparation of the compounds, compositions containing the compounds and the use of the compounds in the prevention or treatment of disorders regulated by the action of ghrelin receptor, including Prader-Willi syndrome, eating disorder, weight gain, weight-loss maintainance following diet and exercise, obesity, and disorders associated with obesity such as noninsulin dependent diabetes mellitus.

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