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625-74-1

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625-74-1 Usage

Description

2-Methyl-1-nitropropane, also known as tert-butyl nitrite, is an organic compound with the chemical formula C4H9NO2. It is a colorless liquid with a characteristic odor and is known for its use as a solvent and in chemical research.

Uses

Used in Chemical Research:
2-Methyl-1-nitropropane is used as a solvent for the discovery and analysis of volatile compounds released by bacterial strains. Its solvent properties allow for the efficient extraction and identification of these compounds, which can be crucial in various scientific and medical applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-methyl-1-nitropropane can be utilized as a solvent in the synthesis of various drugs and active pharmaceutical ingredients. Its ability to dissolve a wide range of substances makes it a valuable asset in the development and production of new medications.
Used in Environmental Science:
2-Methyl-1-nitropropane can also be employed in environmental science as a solvent for the extraction and analysis of pollutants and contaminants in soil, water, and air samples. This helps in the assessment of environmental quality and the development of strategies for pollution control and remediation.

Synthesis Reference(s)

Synthesis, p. 616, 1976 DOI: 10.1055/s-1976-24143

Check Digit Verification of cas no

The CAS Registry Mumber 625-74-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 625-74:
(5*6)+(4*2)+(3*5)+(2*7)+(1*4)=71
71 % 10 = 1
So 625-74-1 is a valid CAS Registry Number.

625-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-nitropropane

1.2 Other means of identification

Product number -
Other names Propane,2-methyl-1-nitro

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:625-74-1 SDS

625-74-1Relevant articles and documents

Photocatalytic degradation of imidacloprid by phosphotungstic acid supported on a mesoporous sieve MCM-41

Feng, Changgen,Li, Yanzhou,Liu, Xia

experimental part, p. 127 - 132 (2012/03/09)

Solid catalysts consisting of polyoxometalates (POM) namely phosphotungstic acid H3PW12O40 (HPW) supported on a mesoporous sieve MCM-41 have been prepared and characterized by FT-IR, X-ray diffraction, nitrogen adsorption and high resolution transmission electron microscope (HRTEM). The HPW/MCM-41 with different HPW loadings from 10 to 60 wt% possess large specific surface area and rather uniform mesopores. Keggin structure of HPW retains on the prepared composite catalysts. The photocatalytic performance of HPW/MCM-41 was examined by degradation of a durable pesticide imidacloprid. It is found that the prepared photocatalysts exhibit high activity under irradiation of 365 nm monochromatic light. For 50 mL of imidacloprid (10 mg/L), conversion of imidacloprid using 20 mg of HPW/MCM-41 with 50 wt% loading level and calcined at 300°C reaches 58.0% after 5 h irradiation. Copyright

Synthesis and Decomposition of the N-Alkyl-N-nitro-O-benzoylhydroxylamines

White, Emil H.,Reefer, John,Erickson, Ronald H.,Dzadzic, Petar M.

, p. 4872 - 4876 (2007/10/02)

Nitration of N-alkyl-O-benzoylhydroxylamines yields the correspondng N-nitro derivatives.At modest temperatures these compounds decompose to yield alkyl benzoates, alkenes, benzoic acid, and nitrous oxide.In the case of primary alkylnitrohydroxylamines, nitroalkanes and alkyl nitrates are also formed.The alkyl benzoates are products of ionic reactions since skeletal rearrangements characteristics of carbonium ions occur.The insensivity of the rates of decomposition to solvent polarity suggests that the rate-determining step is a rearrangement rather than direct ionization.

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