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Home > Encyclopedia > Amiloride hydrochloride

Amiloride hydrochloride

pharmaceutical raw materials
Amiloride hydrochloride structure

Amiloride hydrochloride 

structure
  • CAS No:

    2016-88-8

  • Formula:

    C6H8ClN7O.ClH

  • Chemical Name:

    Amiloride hydrochloride

  • Synonyms:

    2-Pyrazinecarboxamide,3,5-diamino-N-(aminoiminomethyl)-6-chloro-,hydrochloride (1:1);Pyrazinecarboxamide,N-amidino-3,5-diamino-6-chloro-,monohydrochloride;Pyrazinecarboxamide,3,5-diamino-N-(aminoiminomethyl)-6-chloro-,monohydrochloride;N-Amidino-3,5-diamino-6-chloropyrazinamide hydrochloride;N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride;Amiloride hydrochloride;Amipramizide;Colectril;Amiprazide;Nilurid;Amilorid hydrochloride;Amipramidine;Guanamprazine hydrochloride;Midamor;MK-870 hydrochloride;1-(3,5-Diamino-6-chloropyrazinecarboxyl)guanidine hydrochloride

  • Categories:

    Active Pharmaceutical Ingredients  >  Urinary System Drugs

Description

Pale Yellow Solid


Amiloride hydrochloride appears as crystalline solid or very light yellow powder. (NTP, 1992)


Amiloride hydrochloride appears as crystalline solid or very light yellow powder. (NTP, 1992)|Amiloride hydrochloride is a hydrochloride obtained by combining amiloride with one molar equivalent of hydrochloric acid. It has a role as a diuretic and a sodium channel blocker. It contains an amiloride(1+).|A pyrazine compound inhibiting SODIUM reabsorption through SODIUM CHANNELS in renal EPITHELIAL CELLS. This inhibition creates a negative potential in the luminal membranes of principal cells, located in the distal convoluted tubule and collecting duct. Negative potential reduces secretion of potassium and hydrogen ions. Amiloride is used in conjunction with DIURETICS to spare POTASSIUM loss. (From Gilman et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 9th ed, p705)

Amiloride hydrochloride Basic Attributes

266.09

265.025

217-958-2

7M458Q65S3

755847

2811

DTXSID2024452

29339980

Characteristics

159

2.07300

yellow powder

2.11 g/cm3

293.5 °C

628.1ºC at 760 mmHg

333.7ºC

H2O: 50 mg/mL, clear, yellow-green

Store at RT

1.08E-15mmHg at 25°C

145.7 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

Insoluble in water.

Amides and Imides

A halide- and amine-substituted aromatic compound, with amide and acidic salt components. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Safety Information

II

6.1(a)

UN 2811 6.1/PG 3

3

25-36/37/38

36-45-26

UQ2275500

T,Xi

P264, P270, P273, P280, P301+P310, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P405, P501

H301

Flash point data for this material are not available; however, it is probably combustible. (NTP, 1992)

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P273, P280, P301+P310, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P405, and P501|Aggregated GHS information provided by 189 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Fires involving this material can be controlled using a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)

Excerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]: As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2016)

SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. STORAGE PRECAUTIONS: You should store this material in a refrigerator. (NTP, 1992)

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Drug Information

A subclass of sodium channel blockers that are specific for ACID-SENSING SODIUM CHANNELS. (See all compounds classified as Acid Sensing Ion Channel Blockers.)|Agents that promote the excretion of urine through their effects on kidney function. (See all compounds classified as Diuretics.)|A subclass of sodium channel blockers that are specific for EPITHELIAL SODIUM CHANNELS. (See all compounds classified as Epithelial Sodium Channel Blockers.)

SYMPTOMS: Symptoms of exposure to this compound include headache, weakness, fatigue, back, chest, neck, shoulder or extremity pain; nausea, anorexia, vomiting, abdominal pain, hyperkalemia, paresthesias, shock, dizziness, coughing, shortness of breath, depression, nervousness, flaccid paralysis of the extremities, bradycardia, flatulence, skin rash, gas pain, constipation and dyspnea. (NTP, 1992)

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

Amidal

Amiloride hydrochloride Use and Manufacturing

Uses

Sodium channel blocker. Diuretic. It is a weak diuretic. The effect is similar to that of triamcinolone, and it is the most powerful drug among the current sodium excretion steroid potassium diuretics. Used as a weak diuretic

Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients

Computed Properties

Molecular Weight:266.09
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:265.0245633
Monoisotopic Mass:265.0245633
Topological Polar Surface Area:159
Heavy Atom Count:16
Complexity:279
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Extract from the above information

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • OLON S.P.A.

    Italy Italy
    Active
  • Minsheng Group Shaoxing Pharmaceutical Co., Ltd.

    China China
    Active
  • Jiangsu Disainuo Pharmaceutical Co., Ltd.

    China China
    Active

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