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34564-38-0

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34564-38-0 Usage

Functional groups

Acetoxy, bromo, and nitro

Category

Organic compound

Usage

Reagent in organic synthesis

Applications

Synthesis of pharmaceutical compounds and production of fine chemicals

Hazardous nature

Considered a hazardous chemical

Handling and storage

Should be handled and stored with caution

Check Digit Verification of cas no

The CAS Registry Mumber 34564-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,6 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34564-38:
(7*3)+(6*4)+(5*5)+(4*6)+(3*4)+(2*3)+(1*8)=120
120 % 10 = 0
So 34564-38-0 is a valid CAS Registry Number.

34564-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-acetyloxy-2-bromo-2-nitropropyl) acetate

1.2 Other means of identification

Product number -
Other names 2-bromo-1,3-diacetoxy-2-nitro-propane

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:34564-38-0 SDS

34564-38-0Downstream Products

34564-38-0Relevant articles and documents

Simultaneous in-cell derivatization pressurized liquid extraction for the determination of multiclass preservatives in leave-on cosmetics

Sanchez-Prado, Lucia,Lamas, J. Pablo,Lores, Marta,Garcia-Jares, Carmen,Llompart, Maria

experimental part, p. 9384 - 9392 (2011/09/20)

An effective one-step sample preparation methodology for the determination of multiclass preservatives in cosmetics has been developed, applying, for the first time to this kind of matrix, pressurized liquid extraction (PLE) and a very simple, cheap, and fast derivatization procedure: acetylation with acetic anhydride and pyridine. A multifactorial experimental design has been used to evaluate and optimize the main experimental parameters potentially affecting the extraction process. In the final conditions the sample was mixed with Florisil as the dispersing sorbent and extracted with ethyl acetate for 15 min at 120 °C. One of the main goals of this work was to demonstrate the possibility of carrying out direct cosmetic preservative acetylation by simply adding the derivatization reagents into the PLE cell. The extract was then analyzed by GC/MS without any further cleanup or concentration step. The accuracy, precision, linearity, and detection limits (LODs) were evaluated to assess the performance of the proposed method. Quantitative recoveries were obtained, and relative standard deviation values were lower than 10% in all cases. The obtained LODs ranged from 0.000004% to 0.0001% (w/w), values far below the established restrictions in the European Cosmetics Regulation, making this multicomponent analytical method suitable for routine control. Finally, several cosmetic products such as moisturizing and antiwrinkle creams and lotions, hand creams, sunscreen and after-sun creams, baby lotions, and hair care products were analyzed. All the samples contained several of the target cosmetic ingredients, in some cases at quite high concentrations, although the actual European Cosmetics Regulation was fulfilled in all cases.

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