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19-Norethindrone acetate

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Name

19-Norethindrone acetate

EINECS 200-132-0
CAS No. 51-98-9 Density 1.14 g/cm3
PSA 43.37000 LogP 4.06330
Solubility 3.162mg/L(10 oC) Melting Point 161-162°
Formula C22H28O3 Boiling Point 454.7 °C at 760 mmHg
Molecular Weight 340.463 Flash Point 197.1 °C
Transport Information N/A Appearance N/A
Safety 36/37 Risk Codes 40-48
Molecular Structure Molecular Structure of 51-98-9 (19-Norethindrone acetate) Hazard Symbols HarmfulXn
Synonyms

19-Nor-17a-pregn-4-en-20-yn-3-one,17-hydroxy-, acetate (6CI,8CI);17-Acetoxy-19-nor-17a-pregn-4-en-20-yn-3-one;17a-Ethinyl-19-nortestosteroneacetate;17a-Ethinyl-4-estrene-17b-ol-acetate-3-one;17b-Acetoxy-17a-ethinyl-4-estren-3-one;17b-Hydroxy-19-nor-17a-pregn-4-en-20-yn-3-one acetate;19-Norethynyltestosterone acetate;Aygestin;Estalis;Gynovlane;Milli-Anovlar;Milligynon;Miniphase;NSC 22844;Norethindrone 17-acetate;Norethindrone acetate;Norethynyltestosteroneacetate;Norlutate;Norlutin acetate;Orlutate;Primolut-Nor;19-Norpregn-4-en-20-yn-3-one,17-(acetyloxy)-, (17a)-;

Article Data 25

19-Norethindrone acetate Synthetic route

68-22-4

norethisterone

64-19-7

acetic acid

51-98-9

norethisterone acetate

Conditions
ConditionsYield
With sodium carbonate; trifluoroacetic anhydride In benzene for 0.5h; Ambient temperature;96.5%
Stage #1: acetic acid With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In chloroform at 20℃; for 0.5h; Inert atmosphere;
Stage #2: norethisterone With dmap In chloroform for 18h; Inert atmosphere; Reflux;
93%
With dmap; dicyclohexyl-carbodiimide In chloroform at 20℃;91.6%
In trifluoroacetic acid90%
With benzenesulfonyl chloride In pyridine for 48h;79%
68-22-4

norethisterone

75-36-5

acetyl chloride

51-98-9

norethisterone acetate

Conditions
ConditionsYield
With pyridine; dmap In 1,2-dichloro-ethane at 0℃;92%
68-22-4

norethisterone

108-24-7

acetic anhydride

51-98-9

norethisterone acetate

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 50℃;91%
scandium tris(trifluoromethanesulfonate) In acetonitrile86%
With dmap In toluene at 80 - 90℃; for 3h;28 g
2205-78-9

3,17-diacetoxy-19-nor-17βH-pregna-3,5-dien-20-yne

51-98-9

norethisterone acetate

Conditions
ConditionsYield
With tetrahydrofuran; potassium hydroxide
With hydrogenchloride
68-22-4

norethisterone

51-98-9

norethisterone acetate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: methanol.KOH; THF
View Scheme
Multi-step reaction with 2 steps
1: acetic anhydride; toluene-4-sulfonic acid
2: tetrahydrofuran; methanol
View Scheme
methanolic potassium hydroxide

methanolic potassium hydroxide

ether-light petroleum ether

ether-light petroleum ether

2205-78-9

3,17-diacetoxy-19-nor-17βH-pregna-3,5-dien-20-yne

51-98-9

norethisterone acetate

Conditions
ConditionsYield
In tetrahydrofuran; methanol
In tetrahydrofuran; methanol
111-87-5

octanol

51-98-9

norethisterone acetate

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: ammonium chloride; lithium / tetrahydrofuran; ethanol; ammonia; water
2: aluminum isopropoxide; sodium sulfate / methanol; water; cyclohexanone; toluene
3: 1,4-dioxane; methanol; (2S)-N-methyl-1-phenylpropan-2-amine hydrate; ISOPROPYLAMIDE
4: hydrogenchloride / methanol; water
5: acetic anhydride; toluene-4-sulfonic acid
6: tetrahydrofuran; methanol
View Scheme
1091-93-6

3-methoxy-17-hydroxyestra-2,5(10)-diene

51-98-9

norethisterone acetate

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: aluminum isopropoxide; sodium sulfate / methanol; water; cyclohexanone; toluene
2: 1,4-dioxane; methanol; (2S)-N-methyl-1-phenylpropan-2-amine hydrate; ISOPROPYLAMIDE
3: hydrogenchloride / methanol; water
4: acetic anhydride; toluene-4-sulfonic acid
5: tetrahydrofuran; methanol
View Scheme
17976-32-8

3-methoxyestra-2,5(10)-dien-17-one

51-98-9

norethisterone acetate

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 1,4-dioxane; methanol; (2S)-N-methyl-1-phenylpropan-2-amine hydrate; ISOPROPYLAMIDE
2: hydrogenchloride / methanol; water
3: acetic anhydride; toluene-4-sulfonic acid
4: tetrahydrofuran; methanol
View Scheme
19357-36-9

3-methoxy-19-nor-17βH-pregna-2,5(10)-dien-20-yn-17-ol

51-98-9

norethisterone acetate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: hydrogenchloride / methanol; water
2: acetic anhydride; toluene-4-sulfonic acid
3: tetrahydrofuran; methanol
View Scheme

19-Norethindrone acetate Consensus Reports

IARC Cancer Review: Animal Limited Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 21 (1979),p. 441.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Sufficient Evidence IMEMDT    IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 6 (1974),p. 179.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) . EPA Genetic Toxicology Program.

19-Norethindrone acetate Specification

1. Introduction of 19-Norethindrone acetate
19-Norethindrone acetate is one kind of white or almost white crystalline. The IUPAC name of this chemical is [(8R,9S,10R,13S,14S,17R)-17-ethynyl-13-methyl-3-oxo-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl] acetate. We can also call it "Norethindrone Acetate". It belongs to Active Pharmaceutical Ingredients;Acetylenes;Biochemistry;Functionalized Acetylenes;Hydroxyketosteroids;Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone. Solubility: Insoluble in cold water, hot water. Besides, it should be stored in a closed cool and dry place.

2. Properties of 19-Norethindrone acetate
Physical properties about 19-Norethindrone acetate are:
(1)ACD/LogP: 3.99; (2)ACD/LogD (pH 5.5): 3.99; (3)ACD/LogD (pH 7.4): 3.99; (4)ACD/BCF (pH 5.5): 632.47; (5)ACD/BCF (pH 7.4): 632.47; (6)ACD/KOC (pH 5.5): 3520.35; (7)ACD/KOC (pH 7.4): 3520.35; (8)#H bond acceptors: 3; (9)#Freely Rotating Bonds: 2; (10)Polar Surface Area: 43.37 Å2; (11)Index of Refraction: 1.555; (12)Molar Refractivity: 95.13 cm3; (13)Molar Volume: 296.1 cm3; (14)Polarizability: 37.71×10-24cm3; (15)Surface Tension: 46.1 dyne/cm; (16)Density: 1.14 g/cm3; (17)Flash Point: 197.1 °C; (18)Enthalpy of Vaporization: 71.43 kJ/mol; (19)Boiling Point: 454.7 °C at 760 mmHg; (20)Vapour Pressure: 1.87E-08 mmHg at 25°C.

3. Structure Descriptors of 19-Norethindrone acetate
(1)SMILES: O=C4\C=C3/[C@@H]([C@H]2CC[C@]1([C@@H](CC[C@]1(C#C)OC(=O)C)[C@@H]2CC3)C)CC4
(2)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-/m0/s1
(3)InChIKey: IMONTRJLAWHYGT-ZCPXKWAGBE
(4)Std. InChI: InChI=1S/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-/m0/s1
(5)Std. InChIKey: IMONTRJLAWHYGT-ZCPXKWAGSA-N

4. Physical Properties of 19-Norethindrone acetate

Physical Property Value Units Temp (deg C) Source
Melting Point 161.5 deg C   EXP
log P (octanol-water) 3.990 (none)   EST
Water Solubility 5.35 mg/L 25 EXP
Atmospheric OH Rate Constant 1.10E-10 cm3/molecule-sec 25 EST

5. Safety Information of 19-Norethindrone acetate
Risk Codes:40-48
40: Limited evidence of a carcinogenic effect
41: Risk of serious damage to eyes
42: May cause sensitization by inhalation
43: May cause sensitization by skin contact
44: Risk of explosion if heated under confinement
45: May cause cancer
46: May cause heritable genetic damage
48: Danger of serious damage to health by prolonged exposure
Safety Statements 36/37
36: Wear suitable protective clothing
37: Wear suitable gloves
Hence, When you are using this chemical, please be cautious about it as the following: It is danger of serious damage to health by prolonged exposure. When you are using it, wear suitable protective clothing and gloves.

6. Use of 19-Norethindrone acetate
19-Norethindrone acetate can be used as progesterone medicines for irregular menstruation, uterine functional bleeding, endometriosis proge. Norethindrone and acetate in combination with estrogen as contraceptive (oral). It is reasonably anticipated to be a human carcinogen.

7. Preparation of 19-Norethindrone acetate
Norethindrone and Acetic anhydride can used to produce 19-Norethindrone acetate under the consideration of DMAP.

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