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Nandrolone

CAS No.
434-22-0
Chemical Name:
Nandrolone
Synonyms
19-NORTESTOSTERONE;nortestosterone;NANDROLON;Nandrolone Base;NADROLONE;Nandrolone decanoat;C07254;NSC 3351;ndrolone;menidrabol
CBNumber:
CB5681525
Molecular Formula:
C18H26O2
Molecular Weight:
274.4
MDL Number:
MFCD00003664
MOL File:
434-22-0.mol
Last updated:2024-03-22 14:56:24

Nandrolone Properties

Melting point 120-125 °C
alpha D22 +55° (c = 0.93 in chloroform)
Boiling point 357.38°C (rough estimate)
Density 1.0528 (rough estimate)
refractive index 1.4800 (estimate)
Flash point 2℃
storage temp. Controlled Substance, -20°C Freezer
solubility Acetonitrile: 1 mg/ml; Ethanol: 1 mg/ml; Methanol: 1 mg/ml
form A crystalline solid
pka 15.06±0.40(Predicted)
color Dimorphic crystals from CH2Cl2/Et2O
Water Solubility 3.09g/L(25 ºC)
Merck 6365
BRN 2055849
InChIKey NPAGDVCDWIYMMC-IZPLOLCNSA-N
CAS DataBase Reference 434-22-0(CAS DataBase Reference)
FDA UNII 6PG9VR430D
NIST Chemistry Reference Nandrolone(434-22-0)
ATC code A14AB01,S01XA11

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Danger
Hazard statements  H351-H360FD
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
Hazard Codes  Xn,T,F
Risk Statements  20/21/22-64-40-61-60-36-11-38-19
Safety Statements  22-24/25-36/37/39-45-36/37-53-16
RIDADR  UN 1648 3 / PGII
WGK Germany  3
RTECS  KG7964000
HS Code  29372900
NFPA 704
0
3 0

Nandrolone price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich N-050 Nandrolone solution 1.0?mg/mL in acetonitrile, ampule of 1?mL, certified reference material, Cerilliant? 434-22-0 1mL $170 2024-03-01 Buy
Sigma-Aldrich BP257 Nandrolone British Pharmacopoeia (BP) Reference Standard 434-22-0 100MG $255 2024-03-01 Buy
Sigma-Aldrich 1454008 Nandrolone United States Pharmacopeia (USP) Reference Standard 434-22-0 50mg $953 2024-03-01 Buy
Cayman Chemical 21173 Nandrolone ≥98% 434-22-0 1mg $38 2024-03-01 Buy
Cayman Chemical 21173 Nandrolone ≥98% 434-22-0 5mg $93 2024-03-01 Buy
Product number Packaging Price Buy
N-050 1mL $170 Buy
BP257 100MG $255 Buy
1454008 50mg $953 Buy
21173 1mg $38 Buy
21173 5mg $93 Buy

Nandrolone Chemical Properties,Uses,Production

Chemical Properties

Crystalline Solid

Originator

Durabolin,Organon,US,1959

Uses

An anabolic steroid. Controlled substance (anabolic steroid)

Definition

ChEBI: A 3-oxo Delta4-steroid that is estr-4-en-3-one substituted by a beta-hydroxy group at position 17.

Manufacturing Process

An ice-cold solution of 1.5 grams of 19-nortestosterone and 1.5 ml of dry pyridine in 10 ml of dry benzene is prepared and a solution of 1.5 ml of β- phenylpropionyl chloride in 5 ml of dry benzene is added dropwise over a period of about 2 minutes with stirring. The resulting mixture is allowed to stand overnight under an atmosphere of nitrogen and then washed successively with cold 5% aqueous hydrochloric acid solution, cold 2.5% aqueous sodium hydroxide solution, and water. After drying over anhydrous sodium sulfate, the solvent is evaporated to give an almost colorless oil. Recrystallization from methanol gives white crystals of 19-nortestosterone 17- β-phenylpropionate, MP 91° to 92.5°C.

Therapeutic Function

Anabolic

Mechanism of action

Nandrolone facilitates formation of body muscle mass and strengthens the process of osseous tissue development. The main indications for using nandrolone, as well as other anabolic steroids, are abnormal protein anabolism, asthenia, diseases accompanied by protein loss, adrenal insufficiency, steroid diabetes, and prolonged condition of sluggishness.

Safety Profile

Experimental reproductiveeffects. When heated to decomposition it emits acridsmoke and irritating fumes.

Synthesis

Nandrolone, 17|?-hydroxyester-4-en-3-one (29.1.7), is made from estradiol (28.1.17). The phenol hydroxyl group undergoes methylation by dimethylsulfate in the presence of sodium hydroxide, forming the corresponding methyl ether (29.3.1), and then the aromatic ring is reduced by lithium in liquid ammonia, which forms an enol ether (29.3.2). Hydrolyzing this compound with a mixture of hydrochloric and acetic acids leads to the formation of a keto group, and simultaneous isomerization of the double bond from C5¨CC10 to position C4¨CC5 gives the desired nandrolone (29.3.3) [16¨C19]. Upon necessity of using it in the form of acid esters, the product is acylated by corresponding acid derivatives.

Synthesis_434-22-0

734-32-7
434-22-0
Synthesis of Nandrolone from Norandrostenedione
Global( 260)Suppliers
Supplier Tel Email Country ProdList Advantage
Zhejiang J&C Biological Technology Co.,Limited
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Capot Chemical Co.,Ltd.
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View Lastest Price from Nandrolone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Nandrolone pictures 2024-04-25 Nandrolone
434-22-0
US $20.00-10.00 / kg 1kg 98% 20 Hebei Kangcang new material Technology Co., LTD
Nandrolone pictures 2024-04-25 Nandrolone
434-22-0
US $9.00-60.00 / g 10g 99% 10 tons Hebei Kangcang new material Technology Co., LTD
Nandrolone pictures 2024-04-25 Nandrolone
434-22-0
US $230.00 / kg 1kg 99% 1000kg Wuhan Cell Pharmaceutical Co., Ltd
  • Nandrolone pictures
  • Nandrolone
    434-22-0
  • US $20.00-10.00 / kg
  • 98%
  • Hebei Kangcang new material Technology Co., LTD
  • Nandrolone pictures
  • Nandrolone
    434-22-0
  • US $9.00-60.00 / g
  • 99%
  • Hebei Kangcang new material Technology Co., LTD
  • Nandrolone pictures
  • Nandrolone
    434-22-0
  • US $230.00 / kg
  • 99%
  • Wuhan Cell Pharmaceutical Co., Ltd

Nandrolone Spectrum

17-beta-hydroxyoestr-4-en-3-one 17-HYDROXY-13-METHYL-2,6,7,8,9,10,11,12,14,15,16,17-DODECAHYDRO-1H-CYCLOPENTA[A]PHENANTHREN-3-ONE, 5-ANDROSTENEDIONE 17b-hydroxyestra-4-en-3-one 17BETA-HYDROXY-4-ESTREN-3-ONE 17BETA-HYDROXY-19-NORANDROST-4-EN-3-ONE 19-NORANDROSTENOLONE 19-NOR-4-ANDROSTEN-17-BETA-OL-3-ONE menidrabol norandrostenolon nortestonate 4-ESTREN-17BETA-OL-3-ONE NANDROLONE NORANDROSTENOLONE NORTESTOSTERONE, 19- (17beta)-estr-4-en-3-on 17-beta-hydroestr-4-en-3-one 17beta-hydroxy-19-nor-4-androsten-3-one 17-beta-hydroxy-estr-4-en-3-on 17beta-hydroxy-estr-4-en-3-on 19-nortestosterone standard solution 19-nortestosterone--dea schedule iii NANDROLON VETRANAL, 250 MG NANDROLONE, MM(CRM STANDARD) NANDROLONE, BP STANDARD NANDROLONE, 99+% NANDROLONE, USP STANDARD NORTESTOSTERONE, 19-(REAGENT / STANDARD GRADE) NandroloneCypionateBase Nandrolone(19-Nortestosterone) 17β-Hydroxyestra-4-en-3-one 19-Nortestosterone, 17b-Hydroxy-4-estren-3-one, 17β-hydroxy-19-norandrost-4-en-3-one (8R,9S,10R,13S,14S,17S)-17-hydroxy-13-methyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one (17b)-19-Nortestosterone 17b-Hydroxy-19-nor-4-androsten-3-one 17b-Hydroxyestr-4-en-3-one 17b-Nortestosterone 19-Nor-17b-hydroxy-3-ketoandrost-4-ene 4-Estren-17b-ol-3-one 4-Estren-3-one-17b-ol b-Nortestosterone d-13b-Methyl-17b-hydroxygon-4-en-3-one D4-Estren-17b-ol-3-one Estr-4-en-3-one, 17b-hydroxy- (8CI) Estr-4-en-3-one, 17-hydroxy-, (17b)- (9CI) NSC 3351 Oestrenolon 19-NORTESTOSTERONE 98+% NANDROLONE:17BETA-HYDROXYESTRA-4-EN-3-ONE (17)-17-Hydroxyestr-4-en-3-one 17β-Hydroxy-19-norandrost-4-en-3-one, 17β-Hydroxy-4-estren-3-one, 19-Norandrostenolone, 4-Estren-17β-ol-3-one, Nadrolone, Nandrolone 17β-Hydroxy-19-norandrost-4-en-3-one, 17β-Hydroxy-4-estren-3-one, 19-Norandrostenolone, 19-Nortestosterone, 4-Estren-17β-ol-3-one, Nadrolone, Nandrolone 17-Hydroxy-estr-4-en-3-one 17beta-Hydroxyestra-4-en-3-one C07254 Nandrolone BaseDecanoate & derivatives Estr-4-en-3-one,17-hydroxy-, (17b)- ndrolone