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Sulfuric acid, mono(1-methylpropyl) ester, also known as isobutyl hydrogen sulfate, is a chemical compound with the formula C4H10O4S. It is a colorless to pale yellow liquid with a pungent odor, known for its corrosive properties and potential to cause skin, eye, respiratory, and digestive irritation upon contact or ingestion.

3004-76-0

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3004-76-0 Usage

Uses

Used in Chemical Production:
Sulfuric acid, mono(1-methylpropyl) ester is used as a raw material in the production of other chemicals, contributing to the synthesis of various compounds for different applications in the chemical industry.
Used as a Solvent:
In the chemical industry, sulfuric acid, mono(1-methylpropyl) ester is used as a solvent for various substances, facilitating their dissolution and enabling their use in different processes.
Used in Pesticide Formulations:
Sulfuric acid, mono(1-methylpropyl) ester is used as a component in pesticide formulations, enhancing their effectiveness in controlling pests and protecting crops.
Used in Consumer Products:
Although its use is limited due to its corrosive nature, sulfuric acid, mono(1-methylpropyl) ester can be found in some consumer products, where its properties are utilized for specific applications.
It is crucial to handle sulfuric acid, mono(1-methylpropyl) ester with care and use appropriate protective equipment to minimize the risk of adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 3004-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3004-76:
(6*3)+(5*0)+(4*0)+(3*4)+(2*7)+(1*6)=50
50 % 10 = 0
So 3004-76-0 is a valid CAS Registry Number.

3004-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name butan-2-yl sulfate

1.2 Other means of identification

Product number -
Other names sulfuric acid mono-sec-butyl ester

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:3004-76-0 SDS

3004-76-0Upstream product

3004-76-0Relevant academic research and scientific papers

Organic hydroperoxide formation in the acid-catalyzed heterogeneous oxidation of aliphatic alcohols with hydrogen peroxide

Liu, Qifan,Wang, Weigang,Liu, Ze,Wang, Tianhe,Wu, Lingyan,Ge, Maofa

, p. 19716 - 19724 (2014/05/20)

Organic hydroperoxides (ROOH) are reactive species which play significant roles in atmospheric processes, such as acid precipitation, hydroxyl radical cycling and secondary organic aerosol formation. Despite their observation in the atmosphere, our understanding of their formation mechanism is still incomplete. In the present work, ROOH formation was found in the acid-catalyzed heterogeneous oxidation of aliphatic alcohols with hydrogen peroxide. The kinetics and mechanism of acid-catalyzed heterogeneous oxidation of three aliphatic alcohols (2-methyl-2-butanol, 3-buten-2-ol and 2-butanol) with hydrogen peroxide were investigated. Based on the experimental results, tertiary or allyl alcohols may contribute to ROOH formation through this route while secondary alcohols may not. The kinetic experiments were conducted in a rotated wetted-wall reactor coupled to a mass spectrometer at room temperature (298 K) with 40-70 wt% H2SO4 solution. The reactive uptake coefficients were acquired for the first time. The generation and degradation mechanisms of ROOH in acidic media were proposed according to the product information. Once formed, ROOH are found to undergo two degradation pathways: the acid-catalyzed rearrangement reaction and the organic hydrogen peroxysulfate formation pathway. The newly found acid-catalyzed process may occur under certain conditions and influence particle growth in the atmosphere.

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