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ALDOSTERONE

ALDOSTERONE Structure
CAS No.
52-39-1
Chemical Name:
ALDOSTERONE
Synonyms
Reichstein;LECTROCORTIN;REICHSTEIN X;μ100 97% (CP);ALD ELISA;NSC 73856;Aldocorten;Aldocortin
CBNumber:
CB8431679
Molecular Formula:
C21H28O5
Molecular Weight:
360.45
MOL File:
52-39-1.mol
Modify Date:
2024/2/27 22:18:11

ALDOSTERONE Properties

Melting point 170-172°C
alpha D23 +152.2° (anhydr; c = 2 in acetone); D25 +161° (c = 0.1 in chloroform)
Boiling point 412.46°C (rough estimate)
Density 1.28
refractive index 1.6120 (estimate)
Flash point 2℃
storage temp. Sealed in dry,Room Temperature
solubility Acetone (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka 12.98±0.10(Predicted)
form Crystalline Powder
color White
Water Solubility 51.18mg/L(37 ºC)
Merck 13,224
BRN 3224996
CAS DataBase Reference 52-39-1(CAS DataBase Reference)
EPA Substance Registry System Aldosterone (52-39-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H302+H312+H332-H319
Precautionary statements  P210-P280-P305+P351+P338
Hazard Codes  Xi,Xn,F
Risk Statements  36/37/38-36-20/21/22-11
Safety Statements  22-24/25-36-26-36/37-16
RIDADR  UN 1648 3 / PGII
WGK Germany  3
RTECS  TU4523000
22-24-25
HS Code  29372900
NFPA 704
1
1 1

ALDOSTERONE price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) A9477 Aldosterone ≥95% (HPLC) 52-39-1 5MG ₹10586.85 2022-06-14 Buy
Sigma-Aldrich(India) A9477 Aldosterone ≥95% (HPLC) 52-39-1 25MG ₹40030.85 2022-06-14 Buy
Sigma-Aldrich(India) A9477 Aldosterone ≥95% (HPLC) 52-39-1 100MG ₹103367.93 2022-06-14 Buy
Sigma-Aldrich(India) A-096 Aldosterone solution 100?μg/mL in acetonitrile, ampule of 1?mL, certified reference material, Cerilliant? 52-39-1 1ML ₹23514.4 2022-06-14 Buy
Product number Packaging Price Buy
A9477 5MG ₹10586.85 Buy
A9477 25MG ₹40030.85 Buy
A9477 100MG ₹103367.93 Buy
A-096 1ML ₹23514.4 Buy

ALDOSTERONE Chemical Properties,Uses,Production

Description

Aldosterone is a mineralocorticosteroid that takes part in the regulation of electrolytic balance in the organism. Aldosterone lowers excretion of sodium ions from the body, thus increasing their reabsorption and increasing secretion of potassium ions in renal tubules. Being a competitive antagonist of aldosterone, spironlactone blocks aldosterone receptors, thus increasing excretion of sodium, chloride, and corresponding equivalents of water with urine, thus retaining the amount of potassium ions in the organism. Spironolactone is used both individually as well as in combination with thiazides, since it lowers kaliuresis caused by thiazide diuretics.

Chemical Properties

White Solid

Uses

Labelled Aldosterone. Aldosterone is an adrenocortical steroid which exerts regulatory influence on metabolism of electrolytes and water. Biologically active aldosterone isomer; a mineralocorticoid pr oduced by the adrenal cortex that induces urinary excretion of K+ and renal reabsorptioon of Na+. Exists as an equilibrium mixture of the aldehyde and the hemiacetal.

Definition

ChEBI: A pregnane-based steroidal hormone produced by the outer-section (zona glomerulosa) of the adrenal cortex in the adrenal gland, and acts on the distal tubules and collecting ducts of the kidney to cause the conservation of sodium, secretion of potassium, i creased water retention, and increased blood pressure. The overall effect of aldosterone is to increase reabsorption of ions and water in the kidney.

Health Hazard

Aldosterone(Aldocortin; electrocortin; mineralocorticoid; 18-oxocorticosterone): (1)Maintenance of normal electrolyte blood balances;(2)Prolongs survival of adrenalectomized animals;(3)Accelerates gluconeogenesis;(4)Regulates kidney function.

Purification Methods

Crystallise aldosterone from aqueous acetone. It exists in solution as an equilibrium mixture of free aldehyde and its cyclic hemiacetal, favouring the hemiacetal. The 21-acetate crystallises from Me2CO/Et2O or CH2Cl2/EtOAc and has m 198-199o, [] D +121.7o (c 0.7, CHCl3). [Barton et al. J Chem Soc Perkin Trans 1 2243 1975, Beilstein 8 IV 3491.]

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