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37098-43-4

2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE is a high-energy explosive chemical compound derived from cyclohexane, featuring four hydroxyl groups and two nitro groups. Its high explosiveness makes it a critical component in the production of powerful explosives and propellants.
Used in Explosive Industry:
2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE is used as a key ingredient in the production of high-energy explosives such as RDX (royal demolition explosive) for its exceptional explosive properties.
Used in Propulsion Industry:
In the propulsion industry, 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE serves as a propellant in rocket engines, leveraging its high-energy release to generate thrust for space exploration and military applications.
Due to the compound's hazardous nature, its handling, production, and usage are subject to stringent regulations and oversight by government agencies to ensure safety and prevent unauthorized access.

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  • 37098-43-4 Structure

  • Basic information

    1. Product Name: 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE
    2. Synonyms: TIMTEC-BB SBB007697;2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE;1 4-DIDEOXY-1 4-DINITRO-NEO-INOSITOL;1,4-DIDEOXY-1,4-DINITRO-NEOINOSITOL DIHYDRATE;2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE 95%;1 4-DIDEOXY-1 4-DINITRO-NEO-INOSITOL 95%;Zinc02517024
    3. CAS NO:37098-43-4
    4. Molecular Formula: C6H10N2O8
    5. Molecular Weight: 274.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37098-43-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 521.9°Cat760mmHg
    3. Flash Point: 232.4°C
    4. Appearance: /
    5. Density: 1.85g/cm3
    6. Vapor Pressure: 4.52E-13mmHg at 25°C
    7. Refractive Index: 1.635
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE(37098-43-4)
    12. EPA Substance Registry System: 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE(37098-43-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 37098-43-4(Hazardous Substances Data)

37098-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37098-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,9 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37098-43:
(7*3)+(6*7)+(5*0)+(4*9)+(3*8)+(2*4)+(1*3)=134
134 % 10 = 4
So 37098-43-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O8/c9-3-1(7(13)14)4(10)6(12)2(5(3)11)8(15)16/h1-6,9-12H

37098-43-4SDS

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 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE

1.2 Other means of identification

Product number -
Other names 1.4-Didesoxy-1.4-dinitro-neo-inosit

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:37098-43-4 SDS

37098-43-4Relevant articles and documents

Polynitrocarbamates Derived from Nitromethane

Klap?tke, Thomas M.,Krumm, Burkhard,Reith, Thomas

, p. 1474 - 1481 (2017)

A variety of energetic compounds combining nitro with nitrocarbamate groups were synthesized. The precursors, polynitro alcohols, were obtained by the condensation of the readily available starting material nitromethane with the small aliphatic aldehydes formaldehyde and glyoxal. The conversion into carbamates was achieved with the reactive chlorosulfonyl isocyanate (CSI) and a final nitration yielded the polynitrocarbamates. The new compounds were fully characterized, including multinuclear NMR spectroscopy, vibrational analysis, mass spectrometry, differential scanning calorimetry, and elemental analysis. The energies of formation were calculated with the GAUSSIAN program package and the detonation parameters were predicted using the EXPLO5 computer code. Due to the positive oxygen balance (ΩCO) of the presented compounds, their performance data as oxidizers were determined and compared to the common oxidizer ammonium perchlorate.

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