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30833-53-5

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30833-53-5 Usage

Description

Isobutyl hydrogen phthalate is a phthalic acid monoester that is obtained by the formal condensation of one of the carboxy groups of phthalic acid with the hydroxy group of isobutanol. It is a white solid and is known as a phthalate metabolite.

Uses

Isobutyl hydrogen phthalate is used as a plasticizer in the manufacturing of various plastic products, such as vinyl flooring, adhesives, and films. It enhances the flexibility, workability, and durability of the materials.
Used in the Plastics Industry:
Isobutyl hydrogen phthalate is used as a plasticizer for [improving the flexibility, workability, and durability of plastic materials] because of its ability to increase the mobility of polymer chains and reduce the glass transition temperature.
Additionally, isobutyl hydrogen phthalate may be used in other industries, such as the automotive and construction industries, for similar purposes, enhancing the properties of materials used in those sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 30833-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30833-53:
(7*3)+(6*0)+(5*8)+(4*3)+(3*3)+(2*5)+(1*3)=95
95 % 10 = 5
So 30833-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c1-8(2)7-16-12(15)10-6-4-3-5-9(10)11(13)14/h3-6,8H,7H2,1-2H3,(H,13,14)

30833-53-5SDS

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 2-(2-methylpropoxycarbonyl)benzoic acid

1.2 Other means of identification

Product number -
Other names Phthalsaeure-monoisobutylester

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:30833-53-5 SDS

30833-53-5Relevant articles and documents

Palladium-Catalyzed Carboxylate-Assisted Ethoxycarboxylation of Aromatic Acids to Synthesize Monoethyl Phthalate Derivatives with Ethyl Bromodifluoroacetate

Tao, Na,Wang, Jie,Yuan, Chunchen,Zeng, Runsheng,Zhao, Ying-Sheng

, p. 8607 - 8610 (2019/11/03)

A novel and efficient approach for direct carbonation of aromatic acids with ethyl bromodifluoroacetate as the carbonyl source is reported. A broad range of substrates bearing various functional groups were tolerated, leading to monoalkyl phthalate derivatives in moderate to good yields.

Practical selective monohydrolysis of bulky symmetric diesters: Comparing with sonochemistry

Shi, Jianjun,Zhao, Tian,Niwayama, Satomi

, p. 6815 - 6820 (2018/10/20)

The conditions of the practical selective monohydrolysis of symmetric diesters we previously reported have been modified and applied to selective monohydrolysis of bulky symmetric diesters. While ultrasound is generally considered effective for two-phase reactions, its effect actually turned out to be rather marginal. Instead, use of a larger proportion of a polar aprotic co-solvent, DMSO, and aqueous KOH helped enhance the reaction rates and improve the yields of the half-esters. The reactions are simple, mild and practical without special devices.

Ecotoxicity and biodegradation of phthalate monoesters

Scholz, Norbert

, p. 921 - 926 (2007/10/03)

Little is known about the fate and the effects of phthalic acid monoesters. Various of these monoesters ranging from n-butyl to isononyl monoester have been evaluated in respect to their biodegradation behaviour and their acute aquatic toxicity. All esters are readily biodegradable, achieving degradation rates of 90% and more. The acute toxicity values strongly depend on the carbon chain length of the alcohol moiety. The short chain specimen have LC/EC 50 around and above 100 mg/l, with values levelling off to around 30 mg/l for the isononyl monoester.

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