Guanidine hydrochloride
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Guanidine hydrochloride
structure -
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CAS No:
50-01-1
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Formula:
CH5N3.ClH
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Chemical Name:
Guanidine hydrochloride
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Synonyms:
Guanidine,hydrochloride (1:1);Guanidine,monohydrochloride;Guanidinium chloride;Guanidine chloride;Guanidinium hydrochloride;Guanidine hydrochloride;Buffer AL;420-13-3;14317-32-9;15827-40-4;87667-20-7;94369-44-5;106946-18-3;139693-44-0;143504-22-7;915070-50-7;1340579-42-1
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CAS No:
Description
Guanidine HCl, the crystalline compound of strong alkalinity formed by the oxidation of guanine, is a normal product of protein metabolism and a protein denaturant.Target: OthersGuanidine HCl is the most popular protein denaturant. Analysis of unfolding transitions by Guanidine HCl provides several important parameters regarding the mechanism of conformational stability of proteins. Guanidine HCl at low concentrations refolds acid-unfolds apomyoglobin and cytochrome c, stabilizing the mo
DryPowder; DryPowder, Liquid|HYGROSCOPIC CRYSTALLINE POWDER.
Guanidine Hydrochloride is the hydrochloride salt form of guanidine, a strong basic compound with parasympathomimetic activity. Guanidine hydrochloride enhances the release of acetylcholine following a nerve impulse and potentiates acetylcholine actions on muscarinic and nicotinic receptors. It also appears to slow the rates of depolarization and repolarization of muscle cell membranes. (NCI05)|A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.
Guanidine hydrochloride Basic Attributes
95.53140
95.02500
200-002-3
3YQC9ZY4YB
0894
755884
DTXSID7058757
C47551
2925290090
Characteristics
75.89000
-1.7
DryPowder; DryPowder, Liquid
1.3 g/cm3
178 °C
132.9ºC at 760 mmHg
34.2ºC
n20/D 1.465
H2O: 2280 g/L (20 ºC)
Store at RT.
LD50 orally in Rabbit: 655.3 - 907.1 mg/kg LD50 dermal Rabbit > 2000 mg/kg
Safety Information
NONH for all modes of transport
1
R22; R36/38
S22
MF4300000
Xn
Well closed. Dry.
Stable. Hygroscopic. Incompatible with strong oxidizing agents.
P261-P280-P301 + P312 + P330-P304 + P340 + P312-P305 + P351 + P338-P337 + P313
H302 + H332-H315-H319
Combustible.
|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, and P501|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|Aggregated GHS information provided by 380 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Use foam, powder.
Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Wash away remainder with plenty of water. Personal protection: P2 filter respirator for harmful particles.
Well closed. Dry.
Evaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed.
The substance is irritating to the eyes and skin.
NO open flames.
PREVENT DISPERSION OF DUST!
Use local exhaust or breathing protection.
Protective gloves. Protective clothing.
Wear safety goggles or eye protection in combination with breathing protection.
Drug Information
Fresh air, rest.
Rinse skin with plenty of water or shower.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Chloride, Guanidinium
The substance can be absorbed into the body by ingestion.
Cough.
Redness.
Redness. Pain.
Guanidine hydrochloride Use and Manufacturing
Used in organic synthesis and pharmaceutical industry; mainly used as intermediates for medicines, important raw materials for the manufacture of sulfadiazine, sulfamethazine, sulfamethazine and folic acid; used as intermediates in medicine, pesticides, dyes and other organic synthesis body. It can be used to synthesize 2-aminopyrimidine, 2-amino-6-methylpyrimidine, 2-amino-4,6-dimethylpyrimidine, and is used to manufacture sulfadiazine, sulfamethazine, sulfamethazine and other sulfa drugs Intermediate. Guanidine hydrochloride (or guanidine nitrate) reacts with ethyl cyanoacetate to form 2,4-diamino-6-hydroxypyrimidine, which is used to synthesize folic acid, an anti-anemia drug. It can also be used as an antistatic agent for synthetic fibers. Used as an organic synthesis intermediate; used as an antistatic agent for synthetic fibers; a powerful chaotropic agent, used for protein denaturation and subsequent refolding
Flame retardants
Personal care products
100,000 - 500,000 lb
Metal treatment|Guanidine, hydrochloride (1:1): ACTIVE
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients|Cosmetics -> Buffering
Computed Properties
Molecular Weight:95.53
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:1
Exact Mass:95.0250249
Monoisotopic Mass:95.0250249
Topological Polar Surface Area:75.9
Heavy Atom Count:5
Complexity:26.3
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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