AMINOGUANIDINE BICARBONATE
Aminoguanidine bicarbonate is the most commonly used form of aminoguanidine in clinical trials.
Aminoguanidine bicarbonate’s role in combating diabetic vascular dysfunction highlights its clinical relevance in managing diabetes.
Aminoguanidine bicarbonate is a pharmaceutical drug that has been used for the treatment of chronic renal failure and congestive heart failure.
CAS Number: 2582-30-1
EC Number: 219-956-7
Molecular Formula: C2H8N4O3
Molecular Weight: 136.11
Synonyms: aminoguanidinium hydrogen carbonate, Aminoguanidine hicarbonate, 1-aminoguanidine carbonate, Aminoguanidine bicarbonate, GUANYLHYDRAZINE BICARBONATE, Aminoguanidine bicarbonate, Aminoguanidine carbonic acid, 1-Aminoguanidine bicarbonate, Aminoguanidine hydrogen carbonate, 1-AMINOGUANIDINE HYDROGEN CARBONATE, aminoguanidinium hydrogen carbonate, 1-AMINOGUANIDINIUM HYDROGEN CARBONATE, Aminoguanidine bicarbonate CRYSTALLINE, 1-AMINOGUANIDINIUM HYDROGEN CARBONATE OE, Aminoguanidine hydrogencarbonate, Guanylhydrazine hydrogencarbonate, Aminoguanidine bicarbonate, 2582-30-1, Aminoguanidine hydrogen carbonate, 2200-97-7, Aminoguanidinium bicarbonate, 2-aminoguanidine;carbonic acid, Aminoguanidine carbonate, Aminoguanidine carbonate (1:1), Aminoguanidium hydrogen carbonate, Aminoguanidinium hydrogen carbonate, N1-Aminoguanidine carbonate (1:1), Aminoguanidine hydrogencarbonate, MFCD00012949, BA 51-090222, NSC7887, N”-aminoguanidine; carbonic acid, amino(diaminomethylidene)azanium;hydrogen carbonate, AMINOGUANIDINE; CARBONIC ACID, 1-Aminoguanidine bicarbonate, AMINOGUANIDINECARBONATE, 2-aminoguanidine,carbonic acid, Hydrazinecarboximidamide carbonate, NSC 7887, EINECS 219-956-7, Amino guanidine bicarbonate, Guanidine, amino-, hydrogen carbonate, Ba 51-090222 (VAN), N(sup 1)-Aminoguanidine carbonate (1:1), AI3-52138, Guanylhydrazine hydrogencarbonate, UNII-X2151435R9, aminoguandine bicarbonate, EC 219-956-7, SCHEMBL40128, CH6N4.H2CO3, 1-aminoguanidine; carbonic acid, DTXSID2062537, Aminoguanidine bicarbonate, 97%, Amino guanidine hydrogen carbonate, 1-aminoguanidine carbonic acid salt, HB0111, AKOS015894487, AKOS015901290, hydrazinecarboximidamide bicarbonate salt, hydrazinecarboximidamide carbonic acid salt, LS-12944, A0307, F87308, Q27293343, [amino(hydrazinyl)methylidene]azanium hydrogen carbonate, F0001-0859, Carbonic acid compound with hydrazinecarboximidamide (1:1), 2-Aminoguanidinium hydrogen carbonate, Aminoguanidine hydrocarbonate, Aminoguanidine hydrogencarbonate, Aminoguanidinium hydrogen carbonate, Guanylhydrazine hydrogen carbonate, Aminoguanidine bicarbonate, aminoguanidine hydrogen carbonate, aminoguanidinium bicarbonate, aminoguanidine hydrocarbonate, aminoguanidine carbonate 1:1, aminoguanidium hydrogen carbonate, n1-aminoguanidine carbonate 1:1, aminoguanidine hydrogencarbonate, aminoguanidinebicarbonate, hydrazinecarboximidamide carbonate, Carbonic Acid, compd. with Aminoguanidine, Aminoguanidine bicarbonate, Aminoguanidine Hydrogen Carbonate, Hydrazinecarboximidamide Carbonate, 1-Aminoguanidine bicarbonate, Aminoguanidine bicarbonate, Aminoguanidine Carbonate, Aminoguanidine Hydrogen, Aminoguanidine hydrogencarbonate, Guanylhydrazine hydrogencarbonate, Aminoguanidine hydrogencarbonate, Guanylhydrazine hydrogencarbonate, AMINOGUANIDINE HYDROGEN CARBONATE, hydrazinecarboxiMidaMide carbonate, AMINOGUANADINE BICARBONATE, aminoguanidinium hydrogen carbonate, ABGC, 1-AMinoguanidi, AMINOGUANIDINE HCO3, Aminoguanidine bicar, uanidine bicarbonate, Ceramides 100403-19-8, Aminoguanidine hydrogen carbonate, aminoguanidinium hydrogen carbonate, Aminoguanidine hicarbonate, carbonic acid – carbonohydrazonic diamide (1:1), 1-aminoguanidine carbonate, Aminoguanidine carbonic acid, Amino guanidine bicarbonate,
Aminoguanidine bicarbonate is a pharmaceutical drug that has been used for the treatment of chronic renal failure and congestive heart failure.
Aminoguanidine bicarbonate has also been studied for its potential use in Alzheimer’s disease.
Aminoguanidine bicarbonate is the most commonly used form of aminoguanidine in clinical trials.
Aminoguanidine bicarbonate can be synthesized by reacting malonic acid with hydrochloric acid and copper metal hydroxide, which produces copper complexes and Aminoguanidine bicarbonate.
Aminoguanidine bicarbonate inhibits the production of inflammatory cytokines, such as tumor necrosis factor-α and interleukins, and activates endothelial nitric oxide synthase, leading to vasodilation and inhibition of platelet aggregation.
Aminoguanidinium bicarbonate or Aminoguanidine bicarbonate is a chemical compound used as precursor for the preparation of aminoguanidine compounds.
Aminoguanidine bicarbonate has the chemical formula C2H8N4O3.
Aminoguanidine bicarbonate, also referred to as Aminoguanidine hydrogen carbonate, is an organic compound with the molecular formula C2H8N4O3.
Aminoguanidine bicarbonate has a wide range of applications in the pharmaceutical and specialty chemical industries.
The potential of Aminoguanidine bicarbonate to shield cells from adenovirus-induced chromosomal damage showcases Aminoguanidine bicarbonate prowess in cellular defense mechanisms, promising to bolster the immune response against viral infections.
Acting as an inhibitor of NOS, Aminoguanidine bicarbonate exerts control over the intricate nitric oxide synthesis process, paving the way for therapeutic interventions in conditions where excess nitric oxide could cause detrimental effects.
Significantly, Aminoguanidine bicarbonate’s role in combating diabetic vascular dysfunction highlights Aminoguanidine bicarbonate clinical relevance in managing diabetes.
By mitigating vascular impairments associated with diabetes, Aminoguanidine bicarbonate contributes to the preservation of cardiovascular health, potentially reducing the risk of severe complications stemming from diabetic-related vascular issues.
Beyond Aminoguanidine bicarbonate’s biological effects, Aminoguanidine bicarbonate emerges as an indispensable resource in the realm of chemical synthesis.
As a foundational building block for diverse pharmaceuticals, Aminoguanidine bicarbonate empowers researchers and manufacturers to create innovative drugs targeting a wide range of medical conditions.
Additionally, Aminoguanidine bicarbonate’s application in pesticide production fortifies agricultural practices, ensuring enhanced crop protection and improved yields.
Furthermore, Aminoguanidine bicarbonate’s relevance in the production of dyes and foaming agents underscores Aminoguanidine bicarbonate’s significance in the industrial sector.
Aminoguanidine bicarbonate’s unique properties make it an ideal candidate for creating vibrant and durable dyes, catering to various industries such as textiles, cosmetics, and more.
Simultaneously, Aminoguanidine bicarbonate’s capacity as a foaming agent plays a crucial role in the production of numerous consumer products, ranging from personal care items to industrial materials.
Aminoguanidine bicarbonate has chemical structure H2NC(=NH)NHNH2·H2CO3.
Aminoguanidine bicarbonate appears as white crystalline powder.
Aminoguanidine bicarbonate is hygroscopic in nature.
Aminoguanidine bicarbonate or Aminoguanidine hydrogen carbonate or Guanylhydrazine hydrogencarbonate is White crystalline powder, negligibly soluble in water, insoluble in alcohol and other acids.
Aminoguanidine bicarbonate can be used as a raw material for the synthesis of medicines, pesticides, dyes, photographic chemicals and foaming agents.
Aminoguanidine bicarbonate Amino guanidine bicarbonate is used as a drug intermediate.
Aminoguanidine bicarbonate, also known as Aminoguanidine hydrogen carbonate, is an organic compound with the molecular formula C2H8N4O3, highly valued for Aminoguanidine bicarbonate’s applications in the pharmaceutical industry.
In the pharmaceutical sector, Aminoguanidine bicarbonate’s remarkable capabilities shine through.
Aminoguanidine bicarbonate showcases its prowess in cellular defense mechanisms, safeguarding cells from adenovirus-induced chromosomal damage and bolstering the immune response against viral infections.
Additionally, as an effective inhibitor of NOS (nitric oxide synthase), this compound plays a crucial role in controlling the intricate nitric oxide synthesis process.
As a result, Aminoguanidine bicarbonate opens up avenues for therapeutic interventions in conditions where excessive nitric oxide levels could lead to harmful effects.
One of the most significant clinical applications of Aminoguanidine bicarbonate lies in managing diabetes.
By mitigating vascular impairments associated with diabetes, Aminoguanidine bicarbonate actively contributes to preserving cardiovascular health, potentially reducing the risk of severe complications arising from diabetic-related vascular issues.
However, Aminoguanidine bicarbonate’s primary role in the pharmaceutical industry is Aminoguanidine bicarbonate’s utility as a foundational building block for a diverse range of pharmaceuticals.
This unique characteristic empowers researchers and manufacturers to create innovative drugs that target a wide spectrum of medical conditions.
Aminoguanidine bicarbonate is versatility as a raw material plays a pivotal role in advancing drug development and therapeutic solutions, making Aminoguanidine bicarbonate an indispensable resource in the pursuit of better healthcare.
Aminoguanidine bicarbonate is a white solid, slightly soluble in water .
Aminoguanidine bicarbonate is an inhibitor of NOS (nitric oxide synthase).
Aminoguanidine bicarbonate is a white to off-white crystalline powder.
Aminoguanidine bicarbonate is almost insoluble in water, alcohol and other acids.
Aminoguanidine bicarbonate is a chemical compound used as precursor for the preparation of aminoguanidine compounds.
Aminoguanidine bicarbonate has the chemical formula C2H8N4O3.
Aminoguanidine bicarbonate, also known as aminoguanidinium hydrogen carbonate, is a chemical compound used as a precursor for the preparation of aminoguanidine compounds .
Aminoguanidine bicarbonate has the chemical formula C2H8N4O3 .
Aminoguanidine bicarbonate is a white solid, slightly soluble in water .
Aminoguanidine bicarbonate is an inhibitor of NOS (nitric oxide synthase).
Aminoguanidine bicarbonate is an inhibitor of NOS (nitric oxide synthase).
Aminoguanidine bicarbonate, also known as Aminoguanidine hydrogen carbonate, is an organic compound with the molecular formula C2H8N4O3, esteemed for its versatile applications in the specialty chemical industry.
Aminoguanidine bicarbonate, also referred to as Aminoguanidine hydrogen carbonate, is an organic compound with the molecular formula C2H8N4O3.
Aminoguanidine bicarbonate is a chemical compound with the formula CH6N4·H2CO3.
Aminoguanidine bicarbonate is a white crystalline powder that is soluble in water.
Aminoguanidine bicarbonate is a strong nucleophile and a powerful reducing agent.
Aminoguanidine bicarbonate is also a useful reagent for the synthesis of heterocycles.
Uses of Aminoguanidine Bicarbonate:
Aminoguanidine bicarbonate is of practical importance because of its use in dyes, dispersants, explosives and other commercial applications.
Aminoguanidine bicarbonate is used in the synthesis of antitumor agents and antileukemic activity.
Aminoguanidine bicarbonate is also used in the synthesis of neuraminidase inhibitors in the inhibition of influenze.
Aminoguanidine bicarbonate is an inhibitor of NOS (nitric oxide synthase).
Aminoguanidine bicarbonate is used to study the effect of addition of polyamines to rat embryo cell cultures infected with adenovirus type 5.
Synthesis of heterocycles:
Aminoguanidine bicarbonate serves as a reagent for the synthesis of heterocyclic compounds like 1,2,4-triazoles, which have various biological and industrial applications.
Inhibition of nitric oxide synthase:
Aminoguanidine bicarbonate is used to investigate the role of NO in various physiological and pathological processes by inhibiting NOS activity.
Inhibition of advanced glycation end-product (AGE) formation: Aminoguanidine bicarbonate is employed to study the role of AGEs in diabetes, aging, and other conditions.
Wound healing:
Research suggests that Aminoguanidine bicarbonate improves wound healing in diabetic rats by preserving collagen ultrastructure and restoring TGF-β1 expression.
Pulmonary fibrosis:
Studies indicate that aminoguanidine exhibits potential therapeutic effects in preventing pulmonary fibrosis by reducing collagen deposition and hydroxyproline content in the lungs.
Anticonvulsant activity:
Certain derivatives synthesized from Aminoguanidine bicarbonate demonstrate potent anticonvulsant activity, offering potential therapeutic applications in epilepsy.
Energetic materials:
Aminoguanidine bicarbonate serves as a precursor for the synthesis of high-nitrogen-content energetic materials, which find applications in propellants, explosives, and pyrotechnics.
Aminoguanidine is a pharmaceutical drug that has been used for the treatment of chronic renal failure and congestive heart failure.
Aminoguanidine bicarbonate has also been studied for its potential use in Alzheimer’s disease. Aminoguanidine bicarbonate is the most commonly used form of aminoguanidine in clinical trials.
Aminoguanidine bicarbonate can be synthesized by reacting malonic acid with hydrochloric acid and copper metal hydroxide, which produces copper complexes and Aminoguanidine bicarbonate.
Aminoguanidine bicarbonate inhibits the production of inflammatory cytokines, such as tumor necrosis factor-α and interleukins, and activates endothelial nitric oxide synthase, leading to vasodilation and inhibition of platelet aggregation.
Aminoguanidine bicarbonate is an inhibitor of NOS (nitric oxide synthase).
Molecular Structure Analysis of Aminoguanidine Bicarbonate:
Condensation reactions:
Aminoguanidine bicarbonate can react with aldehydes and ketones to form imines, with carboxylic acids to form amides, and with esters to form amidines.
Cyclization reactions:
Aminoguanidine bicarbonate can be used to synthesize heterocycles such as 1,2,4-triazoles.
Nitration reactions:
Aminoguanidine bicarbonate can be nitrated to form nitroguanidine.
Action Mechanism of Aminoguanidine Bicarbonate:
Inhibition of nitric oxide synthase (NOS):
Aminoguanidine bicarbonate acts as an inhibitor of NOS, particularly inducible NOS (iNOS), by competing with L-arginine for the enzyme’s active site.
This inhibition reduces NO production and its downstream effects.
Inhibition of advanced glycation end-product (AGE) formation:
Aminoguanidine bicarbonate interferes with the formation of AGEs, which are implicated in diabetic complications and other pathological conditions.
Aminoguanidine bicarbonate acts as a nucleophile, trapping reactive carbonyl compounds that contribute to AGE formation.
Antioxidant activity:
Aminoguanidine bicarbonate demonstrates antioxidant properties by scavenging reactive oxygen species (ROS) and protecting cells from oxidative stress.
Typical Properties of Aminoguanidine Bicarbonate:
Aminoguanidine bicarbonate is a white fine crystalline powder.
Soft, practically insoluble in water.
Aminoguanidine bicarbonate is insoluble in alcohol and other acids.
Aminoguanidine bicarbonate is unstable when heated, and gradually decomposes when it exceeds 50°C, turns red when Aminoguanidine bicarbonate is heated to 100°C.
In an oil bath, and decomposes completely when Aminoguanidine bicarbonate is heated to 171-173°C.
Aminoguanidine bicarbonate is a white solid, slightly soluble in water.
Aminoguanidine bicarbonate has a density of 1.56 g/cm3 at 20 °C.
Aminoguanidine bicarbonate decomposes when boiled.
Chemical:
Addition of an equimolar amount of freebase aminoguanidine to Aminoguanidine bicarbonate will yield aminoguanidinium carbonate.
Aminoguanidine bicarbonate will react with acids to yield their respective salts.
X-ray analysis has shown that solid Aminoguanidine bicarbonate is actually a zwitterionic molecule, 2-guanidinium-1-aminocarboxylate monohydrate.
Physical:
Aminoguanidinium bicarbonate is a white solid, slightly soluble in water.
Recrystallization from hot water is possible, but some decomposition always occurs and reprecipitation tends to be slow and incomplete.
Biochem/Physiol Actions of Aminoguanidine Bicarbonate:
Aminoguanidine bicarbonate protects the cells infected with adenovirus from chromosomal damage.
Aminoguanidine is a specific and highly effective inhibitor of diamine oxidase present in fetal calf serum.
Synthesis of Aminoguanidine Bicarbonate:
A synthesis method of Aminoguanidine bicarbonate includes reacting an acidic aqueous hydrazine hydrate solution with calcium cyanamide in an elevated temperature to produce an aminoguanidine solution, recovering the solution, and reacting therewith an alkali metal bicarbonate to produce relatively high purity Aminoguanidine bicarbonate.
Synthesis Analysis:
Aminoguanidine bicarbonate can be synthesized by reacting hydrazine hydrate with cyanamide in the presence of carbon dioxide.
The reaction is typically carried out in water at a temperature of 70-80°C.
Aminoguanidine bicarbonate is then isolated by filtration and recrystallized from water.
Aminoguanidine bicarbonate can be prepared by reacting calcium cyanamide with hydrazine sulfate.
Aminoguanidine bicarbonate can also be easily prepared by reducing nitroguanidine with zinc powder.
Another method involves adding zinc powder to a stirred suspension of nitroguanidine in ammonium sulfate solution.
Molecular Structure Analysis:
The molecular weight of Aminoguanidine bicarbonate is 136.1099 g/mol.
The IUPAC Standard InChI name of Aminoguanidine bicarbonate is InChI=1S/CH6N4.CH2O3/c2-1(3)5-4;2-1(3)4/h4H2, (H4,2,3,5); (H2,2,3,4).
Chemical Reactions Analysis:
Aminoguanidine bicarbonate will react with acids to yield their respective salts.
Addition of an equimolar amount of freebase aminoguanidine to Aminoguanidine bicarbonate will yield aminoguanidinium carbonate.
Preparation of Aminoguanidine Bicarbonate:
Aminoguanidine bicarbonate can be prepared by reacting calcium cyanamide with hydrazine sulfate.
Aminoguanidine bicarbonate can also be easily prepared by reducing nitroguanidine with zinc powder.
Diachrynic used this route obtaining a great yield:
41.14 g zinc powder (629 mmol, 3.3 molar eq.) are weighed and put to the side.
Into a reaction flask of at least 500 mL are put 20.00 g nitroguanidine (192 mmol, 1 molar eq.) and 47.62 g of ammonium sulfate (360 mmol, 1.88 molar eq.) in 285 mL of water.
The suspension is stirred and not everything dissolves, this is expected.
The reaction flask is immersed in an ice bath and equipped with magnetic stirring and a thermometer.
Stirring is started.
Once the solution reaches 10 °C the addition of small spatulas of zinc powder at a time is started.
Monitor the exotherm and don’t add too much at once, however the reaction is fairly easy to control.
3-4 spatulas of zinc can be added at a time, making the temperature jump up by 5-8°C.
The reaction was kept between 5-15°C, leaning to the latter temperature.
The complete addition of zinc took about 1 hour, during which the ice bath was refilled just once.
Afterwards the reaction was left stirring at about 15 °C for a further 30 minutes.
The pH rose to about 8-9.
Using a fritted vacuum filter the zinc oxide sludge was removed, Aminoguanidine bicarbonate filtered fairly easily.
The yellow colored filtrate is put into a flask with magnetic stirring, and 8.57 g of 25% ammonia solution (126 mmol, 0.66 molar eq.) are added as well as 28.57 g of sodium bicarbonate (340 mmol, 0.94 molar eq.) with stirring, Aminoguanidine bicarbonate dissolves after a short while.
The solution is left standing for 12 h during which the Aminoguanidine bicarbonate slowly precipitates.
Afterwards Aminoguanidine bicarbonate is vacuum filtered off and air dried.
Yield of Aminoguanidine bicarbonate: 15.700 g (115 mmol, 60% based on nitroguanidine)
Handling And Storage of Aminoguanidine Bicarbonate:
Conditions for safe storage, including any incompatibilities:
Storage conditions:
Tightly closed.
Dry.
Storage class:
Storage class (TRGS 510): 13:
Non Combustible Solids
Stability And Reactivity of Aminoguanidine Bicarbonate:
Reactivity:
No data available
Chemical stability:
Aminoguanidine bicarbonate is chemically stable under standard ambient conditions (room temperature).
Possibility of hazardous reactions:
No data available
Conditions to avoid:
hygroscopic
no information available
First Aid Measures of Aminoguanidine Bicarbonate:
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.
Consult a physician.
In case of eye contact:
After eye contact:
Rinse out with plenty of water.
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
Fire Fighting Measures of Aminoguanidine Bicarbonate:
Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.
Accidental Release Measures of Aminoguanidine Bicarbonate:
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.
Exposure Controls/Personal Protection of Aminoguanidine Bicarbonate:
Personal protective equipment:
Eye/face protection:
Use equipment for eye protection.
Safety glasses:
Skin protection:
Handle with gloves.
Wash and dry hands.
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Body Protection:
protective clothing
Respiratory protection:
Recommended Filter type: Filter type P2
Control of environmental exposure:
Do not let product enter drains.
Identifiers of Aminoguanidine Bicarbonate:
CAS Number: 2582-30-1
EC Number: 219-956-7
MDL number: MFCD00012949
Linear Formula: NH2NHC(=NH)NH2 · H2CO3
Molecular Formula: CH6N4.CH2O3 / C2H8N4O3
CBNumber: CB4114194
Molecular Formula: C2H8N4O3
Molecular Weight: 136.11
MDL Number: MFCD00012949
MOL File: 2582-30-1.mol
CAS Number: 2582-30-1
Molecular Weight: 136.11 g/mol
Beilstein: 3569869
EC Number: 219-956-7
Hill Formula: C₂H₈N₄O₃
Chemical Formula: CH₆N₄ * H₂CO₃
HS Code: 2928 00 90
Storage Temperature: Store below +30°C
Solubility: 2.7 g/L in H2O at 20 °C
pKa: 6.19 at 20 °C
Bulk Density: 700 kg/m³
Chemical Name: Aminoguanidine bicarbonate
IUPAC Name: 2-aminoguanidine; carbonic acid
SMILES: C(=NN)(N)N.C(=O)(O)O
Canonical SMILES: C(=N[NH3+])([NH3+])N.C(=O)([O-])[O-]
Isomeric SMILES: C(=N/[NH3+])([NH3+])/N.C(=O)([O-])[O-]
InChI: InChI=1/CH6N4.CH2O3/c2-1(3)5-4;2-1(3)4/h4H2,(H4,2,3,5);(H2,2,3,4)/p-2
CAS Number: 2582-30-1
Molecular Weight: 136.11 g/mol
Beilstein: 3569869
EC Number: 219-956-7
MDL number: MFCD00012949
Properties of Aminoguanidine Bicarbonate:
Exact Mass: 136.05964013 g/mol
Monoisotopic Mass: 136.05964013 g/mol
Topological Polar Surface Area: 148 Ų
Heavy Atom Count: 9
Complexity: 67.9
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: 2
Compound Is Canonicalized: Yes
Physical State: Crystalline powder
Color: Yellow
Odor: Odorless
Melting Point/Freezing Point: Melting point/range: 170 – 172 °C (decomposition)
Initial Boiling Point and Boiling Range: No data available
Flammability (solid, gas): Aminoguanidine bicarbonate is not flammable.
Upper/Lower Flammability or Explosive Limits: No data available
Flash Point: No data available
Autoignition Temperature: No data available
Decomposition Temperature: No data available
pH: 8.9 at 5 g/l at 20 °C
Viscosity:
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water Solubility: 5 g/l at 25 °C – soluble
Partition Coefficient (n-octanol/water): No data available
Vapor Pressure: No data available
Density: 1.56 g/cm³ at 20 °C
Relative Density: No data available
Relative Vapor Density: No data available
Particle Characteristics: No data available
Explosive Properties: No data available
Oxidizing Properties: None
Other Safety Information: No data available
InChIKey: OTXHZHQQWQTQMW-UHFFFAOYSA-N
BRN: 3569869
Refractive Index: Not available
Specific Gravity: Not available
Hazard Class: Not available
DOT Name: Not available
PubChem CID: 164944
Grade: For synthesis
Assay: 95.00 to 100.00%
Food Chemicals Codex Listed: No
Solubility Information: Solubility in water: Assay Percent Range: 98.5%
Formula Weight: 136.11 g/mol
Percent Purity: 98.50%