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1607-01-8

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1607-01-8 Usage

Description

Pentaerythritol dinitrate (PEDN) is a potent, high explosive organic compound with the chemical formula C5H6N4O12. It is synthesized through the reaction of pentaerythritol with a mixture of concentrated sulfuric and nitric acids. PEDN is recognized for its high oxygen content and stability, which are key factors in its applications.

Uses

Used in Propellant Industry:
Pentaerythritol dinitrate is used as an explosive component for various types of propellants. Its high energy content and stability make it a valuable ingredient in the formulation of these products.
Used in Explosive Industry:
In the explosive industry, Pentaerythritol dinitrate is used as a key ingredient in the production of different kinds of explosives. Its high oxygen content and stability contribute to the effectiveness and reliability of these explosives.
Used in Pyrotechnic Industry:
Pentaerythritol dinitrate is utilized as a component in pyrotechnics due to its explosive properties. It plays a crucial role in the creation of various pyrotechnic effects, such as fireworks and flares.
Used in Medical Applications:
Pentaerythritol dinitrate is used as a vasodilator in the treatment of angina pectoris. It aids in the relaxation of smooth muscle cells within the blood vessels, providing relief from chest pain and improving blood flow.
However, due to its explosive nature, Pentaerythritol dinitrate is categorized as a hazardous substance. It is essential to exercise proper care in its storage and handling to prevent any accidental detonation.

Check Digit Verification of cas no

The CAS Registry Mumber 1607-01-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1607-01:
(6*1)+(5*6)+(4*0)+(3*7)+(2*0)+(1*1)=58
58 % 10 = 8
So 1607-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O8/c8-1-5(2-9,3-14-6(10)11)4-15-7(12)13/h8-9H,1-4H2

1607-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pentaerythritol dinitrate

1.2 Other means of identification

Product number -
Other names -

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:1607-01-8 SDS

1607-01-8Relevant articles and documents

Method for preparing nitro compound by using graphene to catalyze nitric oxide

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Paragraph 0031; 0032, (2018/06/16)

The invention discloses a method for preparing a nitro compound by using graphene to catalyze nitric oxide. A graphene oxide carbon material is used for catalysis of a reaction of nitric oxide and a nitrification substrate such as an aromatic compound to prepare the nitro compound. The method is used for replacing a traditional nitric acid/sulfur acid method to prepare the nitro compound, so thatthe atom utilization rate of the reaction is increased, the energy is saved, and the emission is reduced; and the method has the characteristic of atom economy during industrial preparation of the nitro compound.

Synthesis and study of organic nitrates of heterofunctional series 5. * Synthesis of 3,3-bis(hydroxymethyl)oxetane mono- and dinitrates and 2,2-bis(hydroxymethyl)propane-1,3-diol (pentaerythritol) mono- and dinitrates

Korolev,Eremenko,Meshikhina,Eremenko,Aleksandrov,Konovalova,Lodygina

, p. 1859 - 1863 (2007/10/03)

New procedures were developed for the synthesis of 3,3-bis(hydroxymethyl) oxetane dinitrate (1) by O-nitration of the corresponding glycol (3) or its mononitrate (6), which were prepared by the reactions of 2,2-bis(hydroxymethyl) propane-1,3-diol (pentaerythritol) (2) mono- (4) and dinitrates (5), respectively, with alkali. A new method was devised for the synthesis of compounds 4 and 5 by the reaction of tetraol 2 with concentrated HNO 3 in dichloroethane. The structures of compounds 1 and 6 were established by X-ray diffraction analysis.

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