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616-51-3

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616-51-3 Usage

Physical state

Colorless liquid

Odor

Fruity

Applications

a. Solvent in industrial applications
b. Formulation of paints, coatings, and lacquers
c. Consumer products (nail polish, nail polish removers)
d. Artificial fruit flavorings and fragrances

Properties

a. Low toxicity
b. Low volatility
c. Flammability

Safety

Considered a safer alternative to other solvents due to its low toxicity and low volatility

Appearance

Colorless liquid with a fruity odor

Molecular structure

A branched-chain ester derived from isobutanol and acetic acid

Chemical classification

Ester

Boiling point

Approximately 126-127°C (259-260.6°F)

Density

Approximately 0.868 g/cm3 at 20°C (68°F)

Solubility

Soluble in most organic solvents, slightly soluble in water

Production

Synthesized through the esterification reaction between isobutanol and acetic acid

Environmental impact

Generally considered to have a low environmental impact due to its low volatility and low toxicity

Regulatory status

Subject to various regulations and guidelines depending on the specific application and industry

Storage

Should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames

Health hazards

Prolonged exposure may cause irritation to the eyes, skin, and respiratory system

Precautions

Use appropriate personal protective equipment (PPE) and follow safety guidelines when handling 1,2,2-trimethylpropyl acetate

Disposal

Dispose of in accordance with local, national, and international regulations for hazardous materials.

Check Digit Verification of cas no

The CAS Registry Mumber 616-51-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 616-51:
(5*6)+(4*1)+(3*6)+(2*5)+(1*1)=63
63 % 10 = 3
So 616-51-3 is a valid CAS Registry Number.

616-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,2-trimethylpropyl acetate

1.2 Other means of identification

Product number -
Other names -

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:616-51-3 SDS

616-51-3Downstream Products

616-51-3Relevant articles and documents

Asymmetric transesterification of secondary alcohols catalyzed by feruloyl esterase from Humicola insolens

Hatzakis, Nikos S.,Smonou, Ioulia

, p. 325 - 337 (2007/10/03)

A new asymmetric transesterification of secondary alcohols catalyzed by feruloyl esterase from Humicola insolens has been found. Although alcohols are not the natural substrates for this enzyme, a high R enantioselectivity was observed. Stereochemical studies showed that variations in substrate structure lead to strong variations in enantioselectivity. The highest enantioselectivities are obtained when the β-carbon of the secondary alcohol is tertiary or quaternary.

The Influence of Steric Effects on the Selectivity of Radical CC Bond Formation Reactions

Giese, Bernd,Harnisch, Hanna,Luening, Ulrich

, p. 1345 - 1351 (2007/10/02)

Bulky substituents R1 and R2 at radical 5 decrease the rate of addition to diethyl fumarate to a larger extent than to methyl acrylate (Table 1).The comparison with H-abstraction, which is only slightly influenced by steric effects, shows that 5e (R2 = t-C4H9) reacts at least 235 times slower with diethyl fumarate than 5a (R2 = CH3) (Table 2).Therefore, the stereoselectivity of cyclic radicals 1 (n = 1,2) increases if the CC bond formation reaction is carried out with diethyl fumarate instead of methyl acrylate.

RATIO OF POLAR AND RADICAL PROCESSES IN THERMAL TRANSFORMATIONS OF PEROXIDES. I. EFFECT OF THE LENGTH AND BRANCHING OF THE CHAIN IN THE ALKYL SUBSTITUENT AT THE α-CARBON ATOM OF THE ACYL GROUP

Stankevich, A. I.,Zyat'kov, I. P.,Lazareva, A. M.,El'nitskii, A. P.

, p. 1543 - 1548 (2007/10/02)

Acetyl 2-methylpropionyl, acetyl 2-methylbutyryl, acetyl 2-methyloctanoyl, acetyl 2,3-dimethylbutyryl, and acetyl 2,3,3-trimethylbutyryl peroxides are transformed thermally under the investigated experimental conditions with the formation of the corresponding acyl alkyl carbonates and radical products.The ratio of the polar and radical processes is affected by the length and branching of the chain in the hydrocarbon substituent at the α-carbon atom of the acyl group.

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