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CAS

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31516-52-6

Amidinourea nitrate, also known as guanidinium nitrate, is a chemical compound with the formula C2H7N4O2. It is a white crystalline solid that is soluble in water and is commonly used as a nitrogen-rich fertilizer and a component in some types of explosives. The compound is formed by the reaction of amidinourea with nitric acid, resulting in a product that contains both the amidinourea and nitrate functional groups. Amidinourea nitrate is known for its high nitrogen content, which makes it valuable in agricultural applications, and its potential use in the production of energetic materials due to its explosive properties.

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  • 31516-52-6 Structure

  • Basic information

    1. Product Name: amidinourea nitrate
    2. Synonyms: amidinourea nitrate
    3. CAS NO:31516-52-6
    4. Molecular Formula: C2H7N5O4
    5. Molecular Weight: 165.10808
    6. EINECS: 250-673-1
    7. Product Categories: N/A
    8. Mol File: 31516-52-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 350.6°Cat760mmHg
    3. Flash Point: 165.9°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 2.59E-06mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: amidinourea nitrate(CAS DataBase Reference)
    11. NIST Chemistry Reference: amidinourea nitrate(31516-52-6)
    12. EPA Substance Registry System: amidinourea nitrate(31516-52-6)

  • 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: 31516-52-6(Hazardous Substances Data)

31516-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31516-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,1 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31516-52:
(7*3)+(6*1)+(5*5)+(4*1)+(3*6)+(2*5)+(1*2)=86
86 % 10 = 6
So 31516-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N4O.HNO3/c3-1(4)6-2(5)7;2-1(3)4/h(H6,3,4,5,6,7);(H,2,3,4)

31516-52-6SDS

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 diaminomethylideneurea,nitric acid

1.2 Other means of identification

Product number -
Other names EINECS 250-673-1

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:31516-52-6 SDS

31516-52-6Upstream product

31516-52-6Downstream Products

31516-52-6Relevant articles and documents

The preparation and characterization of guanylurea nitrate and perchlorate salts

Klapoetke, Thomas M.,Sabate, Carles Miro

, p. 301 - 306 (2008)

Guanylurea nitrate (GUN) and guanylurea Perchlorate (GUP) were prepared from cyanoguanidine (CG) and concentrated nitric or perchloric acid, respectively. Both compounds were fully characterized by analytical and spectroscopic methods. Crystals of GUP were grown from water, and its crystal structure was determined by single-crystal X-ray diffraction. GUP crystallizes in the monoclinic space group P21/c with four molecules in the unit cell; different unit cell parameters are a = 8.0115(2) A, b=9.7328(2) A, c = 9.5770(2) A, and β = 105.89(1)°. The heats of combustion of both compounds were determined using oxygen bomb calorimetry. Finally, the EXPLO5 computer code was used to determine the detonation velocity (D = 5734 m s-1) and pressure (P = 10.6 GPa) of GUN as well as those of formulations with ammonium nitrate and dinitramide.

A new procedure to obtain ?-caprolactam catalyzed by a guanidinium salt

Fernández-Stefanuto,Verdía,Tojo

supporting information, p. 12830 - 12834 (2017/11/06)

A new procedure to prepare ?-caprolactam by the Beckmann rearrangement of cyclohexanone oxime is described. Treatment of the oxime with the novel salt cyanoguanidinium tosylate affords ?-caprolactam without the need of any other promoter.

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