PRODUCTS

CYANOGUANIDINE

Cyanoguanidine is used in the manufacture of fertilizers, pharmaceuticals, explosives, oil well drilling muds, and dyestuffs.
Cyanoguanidine is widely used as an industrial intermediate for producing melamine, guanidine derivatives, pharmaceuticals, epoxy curing agents, fertilizers, explosives, and specialty chemicals.
In agriculture, Cyanoguanidine serves as a nitrification inhibitor.

CAS Number: 461-58-5
EC Number: 207-312-8
Molecular Formula: C₂H₄N₄
Molecular Weight: 84.08 g/mol

SYNONYMS:
Cyanoguanidine, Dicyandiamide, Dicyanodiamide, DCD, DICY, N-Cyanoguanidine, 1-Cyanoguanidine, 2-Cyanoguanidine, Guanidine-1-carbonitrile, Guanidine, N-cyano-, Didin, Dicy, DCD, Cyanoguanidine, Dicyanodiamide, N′′-Cyanoguanidine, Cyanoguanidine, Dicyandiamide, Dicyanodiamide, N-cyanoguanidine, 1-cyanoguanidine, Guanidine-1-carbonitrile, Didin, DCD, Dicy, Dicyandiamide, CYANOGUANIDINE, 461-58-5, Dicyanodiamide, N-Cyanoguanidine, 1-Cyanoguanidine, Pyroset DO, Dicyandiamido, Dicyandiamin, Epicure DICY 7, Epicure DICY 15, Araldite HT 986, Bakelite VE 2560, Araldite XB 2879B, Araldite XB 2979B, ACR-H 3636, XB 2879B, DTXSID1020354, AI3-14632, M9B1R0C16H, NSC-2031, J3.635H, DTXCID50354, CHEBI:147423, RefChem:129060, 207-312-8, 2-Cyanoguanidine, Guanidine, cyano-, Metformin EP Impurity A, 3-cyanoguanidine, Guanidine-1-carbonitrile, NSC 2031, MFCD00008066, Guanidine, N-cyano-, NSC2031, aminocyanocarboxamidine, DCD, Dicyandiamin [German], Guanidine-15N3, cyano-15N-, CAS-461-58-5, CCRIS 3478, HSDB 2126, Cyanoguanidine Metformin Related Compound A USP, EINECS 207-312-8, UNII-M9B1R0C16H, Dicyanadiamide, Dicyanediamide, cyano-guanidine, 1-cyano-guanidine, Cyanamide metabolite, Dicyandiamide, 99%, Dyhard 100S, Adeka EH 3636AS, Dicyanodiamide M.P. RS, Adeka EH 3636, Metformin impurity A CRS, DICYANODIAMIDE [MI], EC 207-312-8, SCHEMBL15222, SCHEMBL36859, CYANOGUANIDINE [HSDB], NCN=C(NH2)2, SCHEMBL291941, SCHEMBL315661, SCHEMBL705160, orb1705665, SCHEMBL4650690, CHEMBL3183942, SCHEMBL30886672, MSK6601, Tox21_201513, Tox21_302730, BBL009709, EBC-13140, SBB028162, STL141074, AKOS000118777, AKOS005208673, CCG-214839, FC20647, NCGC00249058-01, NCGC00256355-01, NCGC00259063-01, 157480-33-6, BP-31003, CS-0015691, NS00003801, ST50409136, EN300-21430, D78355, T20390, F358292, Q905401, F0001-1248, METFORMIN HYDROCHLORIDE IMPURITY A [EP IMPURITY], Z203045078, InChI=1/C2H4N4/c3-1-6-2(4)5/h(H4,4,5,6, Cyanoguanidine, >=95.0% (HPLC), pharmaceutical impurity standard, Metformin impurity A, European Pharmacopoeia (EP) Reference Standard, 26591-10-6, 2-, cyanoguanidine, dicyandiamide, hexadecanoyl CoA, palmitoyl CoA, palmitoyl coenzyme A, palmitoyl-(carbonyl-14C)-coenzyme A, palmitoyl-CoA, palmityl-CoA, N-Cyanoguanidine, 1-Cyanoguanidine, 2-Cyanoguanidine, CGNA, Dicyandiamide, Dicyanodiamide, Didin, Epicure DICY, Guanidine, cyano-, Cyanoguanidine, Dicyanodiamide, N-Cyanoguanidine, Pyroset DO, 1-Cyanoguanidine, 2-Cyanoguanidine, Guanidine-1-carbonitrile, NCN=C(NH2)2, Dicyanediamide, Dicyandiamin, ACR-H 3636, Araldite HT 986, Araldite XB 2879B, Araldite XB 2979B, Bakelite VE 2560, Epicure DICY 15, Epicure DICY 7, Guanidine, N-cyano-, NSC 2031, XB 2879B, CYANOGUANIDINE, DICY, DICYANODIAMIDE, DCD, N-Cyanoguanidine, 1-CYANOGUANIDINE, 2-Cyanoguanidine, Metformin impurity A, Metformin EP Impurity A, DSEP

Cyanoguanidine is a guanidine in which one of the amino hydrogens of guanidine itself is substituted by a cyano group.
Cyanoguanidine has a role as a nitrification inhibitor, a fertilizer, an explosive, a curing agent and a flame retardant.
Cyanoguanidine is a nitrile and a member of guanidines.

Cyanoguanidine is a nitrile derived from guanidine.
Cyanoguanidine is a dimer of cyanamide, from which it can be prepared.
Cyanoguanidine is an important nitrogen-rich organic compound belonging to the guanidine and nitrile families.

Cyanoguanidine is more commonly known as Dicyandiamide (DCD) and is the dimerization product of cyanamide.
Cyanoguanidine also functions as a nitrification inhibitor in agriculture, helping improve nitrogen-use efficiency and reduce environmental nitrogen losses.
Cyanoguanidine is a white crystalline nitrogen-rich compound containing two amino groups, one imino nitrogen, and one nitrile group.

Cyanoguanidine is nearly planar in the solid state, and X-ray crystallographic studies confirm that its electronic structure allows resonance stabilization throughout the guanidine portion of the molecule.
Raman spectroscopy also shows that dissolved Cyanoguanidine exists as an equilibrium mixture of amino and imino tautomers, which contributes to its chemical versatility.

USES and APPLICATIONS of CYANOGUANIDINE:
Cyanoguanidine is widely used as an industrial intermediate for producing melamine, guanidine derivatives, pharmaceuticals, epoxy curing agents, fertilizers, explosives, and specialty chemicals.
Because of its high nitrogen content, good thermal stability, and reactive amino and cyano functional groups, Cyanoguanidine is one of the most versatile nitrogen-containing building blocks used in chemical manufacturing.

Cyanoguanidine is used in the manufacture of fertilizers, pharmaceuticals, explosives, oil well drilling muds, and dyestuffs.
Cyanoguanidine has numerous industrial applications because it functions as both a reactive intermediate and a functional additive.
One of Cyanoguanidine's largest industrial uses is the production of melamine, which is widely used in laminates, adhesives, coatings, and molded plastics.

Another major application of Cyanoguanidine is as an epoxy resin curing agent.
Dicyandiamide-cured epoxy systems are widely used in electronic circuit boards, structural adhesives, powder coatings, and composite materials because they provide long storage life before curing and excellent mechanical properties after curing.

In agriculture, Cyanoguanidine serves as a nitrification inhibitor.
Cyanoguanidine slows the microbial conversion of ammonium into nitrate, reducing nitrogen losses through leaching and improving fertilizer efficiency.

Additional industrial applications of Cyanoguanidine include: Pharmaceutical intermediates, Barbiturate synthesis, Guanidine derivative production, Explosive formulations (historically), Nitrocellulose stabilizer, Oil well drilling chemicals, Dye manufacture, Textile chemicals, PVC stabilizer systems, Specialty organic synthesis.
Cyanoguanidine has also been used in the manufacture of acetoguanamine and benzoguanamine through condensation reactions with nitriles.

-Epoxy curing applications of Cyanoguanidine:
One of the most important modern applications is epoxy technology.
Cyanoguanidine acts as a latent curing agent, meaning that epoxy formulations remain stable during storage but cure rapidly when heated.

Advantages include:
Long shelf life
Controlled curing
Excellent adhesion
High mechanical strength
Good electrical insulation
Chemical resistance
Heat resistance

These properties make DICY-cured epoxies particularly valuable for:
Printed circuit boards
Automotive structural adhesives
Aerospace composites
Industrial bonding
Powder coatings

-Agricultural applications of Cyanoguanidine:
Cyanoguanidine has become increasingly important in modern agriculture.
As a nitrification inhibitor, Cyanoguanidine temporarily suppresses soil bacteria responsible for converting ammonium into nitrate.
This provides several benefits:

Improved nitrogen-use efficiency
Reduced nitrate leaching
Lower groundwater contamination risk
Reduced nitrous oxide emissions
Longer fertilizer effectiveness
Improved crop nitrogen availability
The compound may also form naturally during the decomposition of calcium cyanamide fertilizers in soil.

-Pharmaceutical applications of Cyanoguanidine:
Cyanoguanidine is an important pharmaceutical intermediate.
Cyanoguanidine participates in the synthesis of:

Biguanides
Guanidine derivatives
Barbiturates
Specialty heterocyclic compounds
One particularly well-known connection is that Cyanoguanidine is recognized as Metformin Impurity A in pharmaceutical reference standards because of its relationship to biguanide chemistry.

-Industrial characteristics of Cyanoguanidine:
Commercial production typically begins with cyanamide, which undergoes controlled base-catalyzed dimerization to form Cyanoguanidine.
Industrial characteristics include:

High production efficiency
Good storage stability
Easy crystallization
High purity availability
Excellent compatibility with industrial formulations
Low manufacturing cost
Large-scale commercial availability
Its combination of low cost and chemical versatility has made Cyanoguanidine one of the world's most important nitrogen-rich intermediates.

CHEMICAL REACTIVITY of CYANOGUANIDINE:
One of the most valuable characteristics of Cyanoguanidine is its broad synthetic versatility.
Cyanoguanidine undergoes reactions including:
Condensation with nitriles
Cyclization reactions
Guanidine formation
Melamine synthesis
Biguanide formation
Polymer crosslinking
Epoxy curing reactions
The nitrile group provides an additional reactive site while the amino groups participate readily in condensation chemistry.

BENEFITS AND ADVANTAGES of CYANOGUANIDINE:
Cyanoguanidine offers numerous technical advantages.
Cyanoguanidine's high nitrogen content makes it valuable for chemical synthesis.
Cyanoguanidine's reactive amino and nitrile groups allow participation in many industrial reactions.
Cyanoguanidine's latent curing behavior provides exceptional storage stability for epoxy systems.

Major advantages of Cyanoguanidine include:
High nitrogen content
Excellent thermal stability
Low volatility
Good water solubility
Versatile synthetic intermediate
Effective epoxy curing behavior
Long storage life
Improved fertilizer efficiency
Broad industrial compatibility
Cost-effective production

ALTERNATIVE PARENTS of CYANOGUANIDINE:
*Propargyl-type 1,3-dipolar organic compounds
*Carboximidamides
*Organopnictogen compounds
*Imines
*Hydrocarbon derivatives

SUBSTITUENTS of CYANOGUANIDINE:
*Guanidine
*Organic 1,3-dipolar compound
*Propargyl-type 1,3-dipolar organic compound
*Carboximidamide
*Organopnictogen compound
*Hydrocarbon derivative
*Imine
*Aliphatic acyclic compound

CHEMICAL PROPERTIES of CYANOGUANIDINE:
Cyanoguanidine is chemically stable under normal storage conditions but contains highly reactive amino and cyano groups that participate in numerous industrial synthesis reactions.
Important chemical characteristics of Cyanoguanidine include:

Stable crystalline nitrogen-rich compound
Contains one nitrile functional group
Contains guanidine functionality
Nearly planar molecular structure
Exists in tautomeric equilibrium in solution
Strong hydrogen-bonding capability
Low volatility
High thermal stability before decomposition

Cyanoguanidine is incompatible with:
Strong acids
Strong oxidizing agents
Strong bases under certain conditions
Rather than boiling normally, Cyanoguanidine undergoes decomposition when heated to sufficiently high temperatures.

MOLECULAR STRUCTURE AND CHARACTERISTICS of CYANOGUANIDINE:
The molecular structure of Cyanoguanidine consists of two carbon atoms and four nitrogen atoms arranged around a guanidine framework containing a terminal nitrile group.
One particularly interesting characteristic is that Cyanoguanidine is isomeric with ammonium dicyanamide.
Heating ammonium dicyanamide can convert it into Cyanoguanidine through a solid-state rearrangement involving a zwitterionic intermediate.
X-ray crystallography confirms that Cyanoguanidine is almost completely planar, allowing electron delocalization across the guanidine portion of the structure.

Structural characteristics of Cyanoguanidine include:
Planar molecular geometry
Conjugated nitrogen system
Strong intermolecular hydrogen bonding
Resonance stabilization
Amino-imino tautomerism
High nitrogen content (approximately two-thirds of the molecular weight)
These structural features make Cyanoguanidine highly useful as a synthetic intermediate.

THERMAL CHARACTERISTICS of CYANOGUANIDINE:
Cyanoguanidine possesses excellent thermal stability compared with many other nitrogen-rich compounds.
The relatively high melting point allows Cyanoguanidine to withstand numerous industrial processing conditions before decomposition begins.
When heated further, decomposition occurs instead of simple boiling.

Thermal decomposition may generate:
Ammonia
Nitrogen-containing gases
Cyanamide-related fragments
Carbon-containing decomposition products
This controlled decomposition behavior contributes to several industrial applications of Cyanoguanidine, including epoxy curing systems.

SOLUBILITY BEHAVIOR of CYANOGUANIDINE:
Cyanoguanidine exhibits moderate water solubility while remaining much less hydrophobic than many organic intermediates.
Cyanoguanidine dissolves readily in:
Water
Acetone
Ethanol
Its negative Log P value indicates that Cyanoguanidine strongly prefers aqueous environments over nonpolar organic phases.
These solubility properties of Cyanoguanidine are important in fertilizer formulations, resin chemistry, and pharmaceutical manufacturing.

PRODUCTION AND USE of CYANOGUANIDINE:
Cyanoguanidine is produced by treating cyanamide with base.
Cyanoguanidine is produced in soil by decomposition of cyanamide.

A variety of useful compounds are produced from Cyanoguanidine, guanidines and melamine.
For example, acetoguanamine and benzoguanamine are prepared by condensation of cyanoguanidine with the nitrile:
(H2N)2C=NCN + PhCN → 1,3-(H2N)-5-Ph(C3N3)

Cyanoguanidine is also used as a nitrification inhibitor in stabilized nitrogen fertilizers.
Cyanoguanidine is used in the adhesive industry as a curing agent for epoxy resins.

Formerly, Cyanoguanidine was used as a fuel in some explosives, and may be used as a stabilizer for nitrocellulose.
Cyanoguanidine was patented for use in the synthesis of methylphenobarbital.

CHARACTERISTICS of CYANOGUANIDINE:
Cyanoguanidine is a white crystalline, nitrogen-rich guanidine derivative that combines excellent thermal stability with remarkable synthetic versatility.
Its reactive amino and nitrile groups make Cyanoguanidine one of the most important industrial intermediates used in the production of melamine, guanidine compounds, pharmaceuticals, epoxy curing systems, and agricultural nitrification inhibitors.

Cyanoguanidine's greatest strengths are high nitrogen content, low volatility, good thermal stability, latent epoxy-curing behavior, and broad industrial applicability.
These characteristics have made Dicyandiamide an essential chemical in polymer manufacturing, agriculture, pharmaceuticals, specialty chemicals, and advanced adhesive technologies.

CHEMISTRY of CYANOGUANIDINE:
The structure has been confirmed by X-ray crystallography.
The molecule is planar with two primary amine groups attached to an imino nitrile.

According to Raman spectroscopy measurements, solutions also contain a tautomer, (H2N)HN=CN(H)CN.
Cyanoguanidine is isomeric to ammonium dicyanamide, from which it may be prepared by heating in a closed vessel.
The reaction proceeds via a zwitterionic intermediate, analogous to the Wöhler synthesis of urea from ammonium cyanate.

Cyanoguanidine, also known as DICY or adeka eh 3636, belongs to the class of organic compounds known as guanidines.
Guanidines are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.
Based on a literature review a significant number of articles have been published on cyanoguanidine.

PHYSICAL and CHEMICAL PROPERTIES of CYANOGUANIDINE:
Chemical Name: Cyanoguanidine
Common Name: Dicyandiamide (DCD)
IUPAC Name: N-Cyanoguanidine
CAS Number: 461-58-5
EC Number: 207-312-8
Molecular Formula: C₂H₄N₄
Molecular Weight: 84.08 g/mol
PubChem CID: 10005
ChemSpider ID: 9611
Chemical Class: Guanidine derivative, Nitrile, Nitrogen-rich organic compound

Appearance: White crystalline powder or crystals
Physical State: Solid
Physical State: Solid
Appearance: White crystalline powder or crystals
Color: White
Odor: Practically odorless
Molecular Formula: C₂H₄N₄
Molecular Weight: 84.08 g/mol
Melting Point: 208–211°C
Boiling Point: Approximately 252°C (decomposes)
Density: 1.40 g/cm³
Bulk Density: Approximately 400 kg/m³

Vapor Pressure: 0.001 Pa at 20°C
Refractive Index: 1.626
Water Solubility: 32 g/L at 20°C
Solubility in Acetone: Soluble
Solubility in Ethanol: Soluble
Storage Temperature: 2–8°C recommended
pKa: Approximately 0.73 (predicted)
Log P: −1.0 to −1.5
Henry's Law Constant: 4.3 × 10⁴ mol/(m³·Pa)
Linear Formula: NH2C(=NH)NHCN
CAS Number: 461-58-5

Molecular Weight: 84.08
UNSPSC Code: 12352100
NACRES: NA.22
PubChem Substance ID: 24894150
EC Number: 207-312-8
Beilstein/REAXYS Number: 605637
MDL Number: MFCD00008066
Assay: 99%
Form: powder
Chemical Formula: C2H4N4
Molar Mass: 84.082 g·mol−1

Appearance: White crystals
Density: 1.4 g/cm3
Melting Point: 209.5 °C (409.1 °F; 482.6 K)
Boiling Point: 252 °C (486 °F; 525 K)
Solubility in Water: 41.3 g/L[1]
Solubility in Acetone: soluble
Solubility in Ethanol: soluble
Log P: −1.5 (est)[2]
Henry's Law Constant (kH): 2.25×10−10 (atm·m3)/mol
Acidity (pKa): 14.8[1]
Basicity (pKb): 14.4[1]
Magnetic Susceptibility (χ): −44.55×10−6 cm3/mol

Physical State: solid (20 °C, 1.013 hPa)
Color: colourless
Odor: odourless
Odor Threshold: Not applicable
Melting Point/Range: 208 - 211 °C
Method: lit.
Boiling Point: No data available
Flammability: No data available
Upper Explosion Limit/Upper Flammability Limit: No data available
Lower Explosion Limit/Lower Flammability Limit: No data available
Flash Point: No data available
Autoignition Temperature: No data available

Decomposition temperature: > 170 °C
pH : No data available
Viscosity, dynamic : No data available
Viscosity, kinematic : No data available
Flow time : No data available
Water solubility : No data available
Partition coefficient: noctanol/water: Pow: 0,1 (20 °C)
log Pow: -1 (20 °C)
pH: 7,4
Method: OECD Test Guideline 107
GLP: yes
Bioaccumulation is not expected.

Vapor pressure : No data available
Relative density : No data available
Density : 1,4 g/cm3 (20 °C)
Relative vapour density : No data available
Explosives : Not classified as explosive.
Oxidizing properties : none
Burning rate : No data available
Evaporation rate : No data available
Molecular weight : 84,08 g/mol
Molecular Weight: 84.08 g/mol
XLogP3: -1.2

Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 2
Rotatable Bond Count: 0
Exact Mass: 84.043596145 Da
Monoisotopic Mass: 84.043596145 Da
Topological Polar Surface Area: 88.2 Å²
Heavy Atom Count: 6
Formal Charge: 0
Complexity: 100
Isotope Atom Count: 0

Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Other (deleted CASRN): 125148-58-5
ECHA EINECS - REACH Pre-Reg: 207-312-8
FDA UNII: M9B1R0C16H
Nikkaji Web: J3.635H
Beilstein Number: 605637

MDL: MFCD00008066
XlogP3: -1.20 (est)
Molecular Weight: 84.08188000
Formula: C2 H4 N4
Appearance: white crystalline powder (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 211.00 °C. @ 760.00 mm Hg
Boiling Point: 229.00 to 230.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.068000 mmHg @ 25.00 °C. (est)

Flash Point: 32.00 °F. TCC (0.00 °C.) (est)
logP (o/w): -1.150
Soluble in: water, 4.13E+04 mg/L @ 25 °C (exp)
Chemical Formula: C2H4N4
Average Molecular Weight: 84.082
Monoisotopic Molecular Weight: 84.043596145
IUPAC Name: N-cyanoguanidine
Traditional Name: 2-cyanoguanidine
CAS Registry Number: Not Available
SMILES: NC(=N)NC#N

InChI Identifier: InChI=1S/C2H4N4/c3-1-6-2(4)5/h(H4,4,5,6)
InChI Key: QGBSISYHAICWAH-UHFFFAOYSA-N
Melting Point: 208-211 °C (lit.)
Boiling Point: 144.35°C (rough estimate)
Density: 1.40
Bulk Density: 400kg/m3
Vapor Pressure: 0.001 Pa at 20°C
Refractive Index: 1.6260 (estimate)
Storage Temperature: 2-8°C
Solubility: H₂O : 0.1 g/mL, clear
pKa: 0.73±0.70 (Predicted)
State of Matter: Crystalline Powder
Color: White

Biological Source: rabbit
Water Solubility: 32 g/L (20 ºC)
Merck: 14,3092
BRN: 605637
Henry's Law Constant: 4.3×10 4 mol/(m 3 Pa) at 25℃, HSDB (2015)
Stability: Stable. Incompatible with strong acids, strong oxidizing agents, strong bases.
InChI: 1S/C2H4N4/c3-1-6-2(4)5/h(H4,4,5,6)
InChIKey: QGBSISYHAICWAH-UHFFFAOYSA-N
SMILES: NC(=N)NC#N
LogP: -1 at 20℃
CAS Database: 461-58-5 (CAS DataBase Reference)
NIST Chemical Information: Dicyandiamide (461-58-5)
EPA Chemical Information: Dicyanodiamides (461-58-5)

FIRST AID MEASURES of CYANOGUANIDINE:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available

ACCIDENTAL RELEASE MEASURES of CYANOGUANIDINE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of CYANOGUANIDINE:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of CYANOGUANIDINE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of CYANOGUANIDINE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.

STABILITY and REACTIVITY of CYANOGUANIDINE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Possibility of hazardous reactions:
No data available

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