| Identification | More | [Name]
19-Norethindrone acetate | [CAS]
51-98-9 | [Synonyms]
17a-ethynyl-19-nortestosterone 17b-acetate
17ALPHA-ETHYNYL-17BETA-HYDROXY-19-NOR-4-ANDROSTEN-3-ONE 17-ACETATE
17ALPHA-ETHYNYL-19-NORTESTOSTERONE 17BETA-ACETATE
17ALPHA-ETHYNYL-19-NORTESTOSTERONE ACETATE
17-hydroxy-19-nor-17a-4-pregnen-20-yn-3-one acetate
17-HYDROXY-19-NOR-17ALPHA-4-PREGNEN-20-YN-3-ONE ACETATE
19-NOR-17ALPHA-ETHYNYLTESTOSTERONE ACETATE
19-NORESTHISTERONE ACETATE
19-NORETHINDRONE ACETATE
19-NORETHISTERONE 17-ACETATE
19-NORETHISTERONE ACETATE
4-ESTREN-17ALPHA-ETHYNYL-17BETA-OL-3-ONE 17-ACETATE
4-ESTREN-17-ALPHA-ETHYNYL-17-BETA-OL-3-ONE ACETATE
ACETIC ACID 17-ETHYNYL-13-METHYL-3-OXO-2,3,6,7,8,9,10,11,12,13,14,15,16,17-TETRADECAHYDRO-1H-CYCLOPE
NORETHINDRONE ACETATE
NORETHISTERONE ACETATE
(17-alpha)-17-(Acetyloxy)-19-norpregn-4-en-20-yn-3-one
(17α)-17-(acetyloxy)-19-norpregn-4-en-20-yn-3-one
17-acetoxy-19-nor-17-alpha-pregn-4-en-20-yn-3-on
17-acetoxy-19-nor-17-alpha-pregn-4-en-20-yn-3-one | [EINECS(EC#)]
200-132-0 | [Molecular Formula]
C22H28O3 | [MDL Number]
MFCD04039850 | [Molecular Weight]
340.46 | [MOL File]
51-98-9.mol |
| Chemical Properties | Back Directory | [Melting point ]
161-162° | [Boiling point ]
416.25°C (rough estimate) | [density ]
1.1236 (rough estimate) | [refractive index ]
-34 ° (C=1, Dioxane) | [storage temp. ]
2-8°C | [solubility ]
Practically insoluble in water, freely soluble in methylene chloride, soluble in alcohol. | [form ]
neat | [color ]
Crystals from Me2CO/hexane | [Water Solubility ]
3.162mg/L(10 ºC) | [Merck ]
6697 | [Major Application]
pharmaceutical small molecule | [InChI]
InChI=1/C22H28O3/c1-4-22(25-14(2)23)12-10-20-19-7-5-15-13-16(24)6-8-17(15)18(19)9-11-21(20,22)3/h1,13,17-20H,5-12H2,2-3H3/t17-,18+,19+,20-,21-,22-/s3 | [InChIKey]
IMONTRJLAWHYGT-ZCPXKWAGSA-N | [SMILES]
C[C@]12CC[C@]3([H])[C@@]4([H])CCC(=O)C=C4CC[C@@]3([H])[C@]1([H])CC[C@]2(C#C)OC(=O)C |&1:1,4,6,16,18,22,r| | [CAS DataBase Reference]
51-98-9(CAS DataBase Reference) | [NIST Chemistry Reference]
Norethindrone acetate(51-98-9) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R40:Limited evidence of a carcinogenic effect.
R48:Danger of serious damage to health by prolonged exposure. | [Safety Statements ]
S36/37:Wear suitable protective clothing and gloves . | [WGK Germany ]
3
| [RTECS ]
RC8965000
| [HS Code ]
29372390 | [Storage Class]
6.1D - Non-combustible acute toxic Cat.3
toxic hazardous materials or hazardous materials causing chronic effects | [Hazard Classifications]
Aquatic Acute 1
Aquatic Chronic 1
Carc. 2
Lact.
Repr. 1A | [Safety Profile]
Suspected carcinogen with experimental tumorigenic data. Human reproductive effects by ingestion and implant routes: menstrual cycle changes, postpartum effects, and changes in fertility. A human teratogen by an unspecified route with developmental abnormalities of the urogenital system. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. Used in the treatment of menstrual dsorders and uterine bleedmg. | [Toxicity]
dlt-mus-orl 1120 mg/kg/4W MUREAV 26,535,74 |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Originator]
Norlestrin,Parke Davis ,US,1964 | [Uses]
Oral contraceptive (in combination with estrogen) | [Uses]
Progesteron. Norethindrone and acetate in combination with estrogen as contraceptive (oral). It is reasonably anticipated to be a human carcinogen. | [Definition]
ChEBI: A 3-oxo Delta4-steroid that is norethisterone in which the hydroxy group has been converted to its acetate ester. | [Manufacturing Process]
2.98 grams of 17-ethinyl-19-nor-testosterone (norethindrone) are suspended in 30 cc of acetic anhydride and a solution of 1.9 grams of p-toluenesulfonic acid in 19 cc of acetic anhydride is gradually added while cooling and stirring. Complete dissolution takes place after about one hour. After additional 30 to 60 minutes, a thick, pasty mass separates. The reaction is permitted to continue for a total period of 5 hours, whereupon water is added to the reaction mixture and the 3-enol-17-diacetate which separates after stirring for 1 to 2 hours is filtered off, washed until neutral and dried in vacuo over calcium chloride at room temperature.
In order to prepare the monoacetate, the crude diacetate is suspended in 150 cc of methanol and, after adding 1.5 cc, concentrated hydrochloric acid, heated to boiling for 15 minutes in a nitrogen atmosphere. The crude monoacetate which separates upon the addition of water after cooling is filtered off, washed and dried in vacuo over calcium chloride at room temperature. The pure 17-acetete, obtained after repeated recrystallizations from methylene chloride/hexane has a MP of 161° to 162°C.
| [Brand name]
Aygestin (Duramed); Norlutate (Parke-Davis). | [Therapeutic Function]
Chemical Name: 19-Nor-17α-pregn-4-en-20-yn-3one, 17-hydroxy-, acetate
| [General Description]
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|