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595-86-8

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595-86-8 Usage

Appearance

Pale yellow, crystalline solid

Explosiveness

Highly explosive

Toxicity

Toxic

Uses

a. Production of explosives
b. Propellant in rocket fuel
c. Reagent in organic synthesis reactions

Regulation

Tightly regulated and strictly controlled

Health hazards

a. Severe skin irritation
b. Severe eye irritation
c. Respiratory system issues
d. Digestive system issues

Safety precautions

Handle and store with extreme caution, follow all safety protocols to prevent accidents and exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 595-86-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 595-86:
(5*5)+(4*9)+(3*5)+(2*8)+(1*6)=98
98 % 10 = 8
So 595-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H3N3O6/c1-2(3(6)7,4(8)9)5(10)11/h1H3

595-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trinitroethane

1.2 Other means of identification

Product number -
Other names Trinitroaethan

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:595-86-8 SDS

595-86-8Relevant articles and documents

INTERPHASE ANALYSIS IN THE CHEMISTRY OF ALIPHATIC NITRO COMPOUNDS. 1. ALKYLATION OF ALKALI METAL SALTS OF TRINITROMETHANE UNDER INTERPHASE CATALYSIS CONDITIONS IN SOLID PHASE-LIQUID SYSTEMS

Shevelev, S. A.,Dalinger, L. I.,Vinogradov, V. M.,Fainzil'berg, A. A.

, p. 1647 - 1650 (1990)

Methylation of trinitromethane salts was studied under interphase catalysis conditions in a solid phase (a trinitromethane salt)-liquid (methyl iodide) system in the presence of interphase transfer catalysts - onium salts, cyclic and acyclic polyethers.The dependence of the yield of the methylation product - 1,1,1-trinitroethane - on the nature of the catalyst was also investigated, and based on this, catalysts were found, in whose presence the methylation process is realized more effectively than under homogeneous conditions.

REACTION OF DINITROMETHYL COMPOUNDS WITH XENON DIFLUORIDE IN VARIOUS SOLVENTS

Tselinskii, I. V.,Mel'nikov, A. A.,Trubitsin, A. E.

, p. 1485 - 1487 (2007/10/02)

The products from the reaction of xenon difluoride with the potassium salts of a series of dinitromethyl compounds ( dinitromethane, trinitromethane, 1,1-dinitroethane, phenyldinitromethane) in methylene chloride, carbon tetrachloride, and acetonitrile were investigated.On the basis of the data from analysis by GLC and UV spectroscopy it was found that in most cases the reaction takes place with the participation of solvent molecules.The proposed reaction mechanism includes a stage of one-electron oxidation of the anion of the dinitromethyl compound by the XeF2 molecule to a dinitromethyl radical.

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