Product Name

  • Name

    Methylprednisolone

  • EINECS 201-476-4
  • CAS No. 83-43-2
  • Article Data19
  • CAS DataBase
  • Density 1.28 g/cm3
  • Solubility 0.12g/L(25 oC)
  • Melting Point 228-237 °C (dec.)
  • Formula C22H30O5
  • Boiling Point 571.8 °C at 760 mmHg
  • Molecular Weight 374.477
  • Flash Point 313.7 °C
  • Transport Information
  • Appearance White to off-white crystalline powder
  • Safety 22-36-26
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 83-43-2 (Methylprednisolone)
  • Hazard Symbols IrritantXi
  • Synonyms Pregna-1,4-diene-3,20-dione,11b,17,21-trihydroxy-6a-methyl- (7CI,8CI);11b,17,21-Trihydroxy-6a-methylpregna-1,4-diene-3,20-dione;6a-Methyl-11b,17a,21b-trihydroxy-1,4-pregnadiene-3,20-dione;6a-Methylprednisolone;Besonia;Duralone;M-Prednisol;Medorol;Medralone;Medrol;Metastab;Metilbetasone;Metrisone;NSC 19987;Prednol;Promacortine;Suprametil;Urbason;Urbasone;Wyacort;Methylphenisolone;
  • PSA 94.83000
  • LogP 1.80360

Synthetic route

methylprednisolone acetate
53-36-1

methylprednisolone acetate

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Hydrolysis;
With potassium hydroxide In methanol; dichloromethane at 10 - 15℃; for 0.333333h; Inert atmosphere;
(20Ξ)-11β-hydroxy-6α-methyl-17,20;20,21-bis-methylenedioxy-pregna-1,4-dien-3-one
117888-35-4

(20Ξ)-11β-hydroxy-6α-methyl-17,20;20,21-bis-methylenedioxy-pregna-1,4-dien-3-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
With formic acid
methylprednisolone acetate
53-36-1

methylprednisolone acetate

A

Methylprednisolone
83-43-2

Methylprednisolone

B

17α-acetoxy-11β,21-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione
86401-94-7

17α-acetoxy-11β,21-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione

Conditions
ConditionsYield
With aq. buffer In N,N-dimethyl-formamide at 25℃; Rate constant; Mechanism; pH dependence;
17α-acetoxy-11β,21-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione
86401-94-7

17α-acetoxy-11β,21-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione

A

Methylprednisolone
83-43-2

Methylprednisolone

B

methylprednisolone acetate
53-36-1

methylprednisolone acetate

Conditions
ConditionsYield
With aq. buffer In N,N-dimethyl-formamide at 25℃; Rate constant; Mechanism; pH dependence;
6α-methylprednisolone-21-hydrogen succinate
2921-57-5

6α-methylprednisolone-21-hydrogen succinate

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
With tetramethyl ammoniumhydroxide; tetrazolium blue In ethanol Rate constant; Ambient temperature; reaction of corticosteroids and their hemisuccinate esters with blue tetrazolium under USP assay conditions, hydrolysis of esters, effect of water content, kinetic study by HPLC;
With water In acetonitrile at 25℃; Rate constant;
In water at 25℃; Rate constant; rate constants for hydrolysis;
6α-methylprednisolone-21-hydrogen succinate
2921-57-5

6α-methylprednisolone-21-hydrogen succinate

A

Methylprednisolone
83-43-2

Methylprednisolone

B

6α-methylprednisolone 17-hemisuccinate
77074-42-1

6α-methylprednisolone 17-hemisuccinate

Conditions
ConditionsYield
With aq. buffer In N,N-dimethyl-formamide at 25℃; Rate constant; Mechanism; pH dependence;
6α-methylprednisolone 17-hemisuccinate
77074-42-1

6α-methylprednisolone 17-hemisuccinate

A

Methylprednisolone
83-43-2

Methylprednisolone

B

6α-methylprednisolone-21-hydrogen succinate
2921-57-5

6α-methylprednisolone-21-hydrogen succinate

Conditions
ConditionsYield
With aq. buffer In N,N-dimethyl-formamide at 25℃; Rate constant; Mechanism; pH dependence;
6α-methylprednisolone 21-hemiadipate
85847-50-3

6α-methylprednisolone 21-hemiadipate

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
With water In acetonitrile at 25℃; Rate constant;
6α-methylprednisolone 21-hemisuberate
85847-51-4

6α-methylprednisolone 21-hemisuberate

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
With water In acetonitrile at 25℃; Rate constant;
17,21-dihydroxy-pregn-4-ene-3,11,20-trione
53-06-5, 10007-36-0, 15779-07-4, 35446-72-1, 104713-00-0

17,21-dihydroxy-pregn-4-ene-3,11,20-trione

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 9 steps
1: aqueous hydrochloric acid; chloroform
2: benzene; toluene-4-sulfonic acid
3: peroxybenzoic acid; benzene / Behandeln unter Ausschluss von Licht, Behandeln des Reaktionsprodukts mit Ameisensaeure und Erwaermen des danach isolierten Reaktionsprodukts mit wss.-methanol. Kalilauge
4: toluene-4-sulfonic acid
5: benzene; diethyl ether
6: pyridine; thionyl chloride / Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether und Benzol
7: acetone; toluene-4-sulfonic acid
8: acetic acid; tert-butyl alcohol; selenium dioxide
9: aqueous formic acid
View Scheme
11β,21-dihydroxy-6α-methyl-pregna-4,17(20)c-dien-3-one
3386-04-7, 14423-17-7

11β,21-dihydroxy-6α-methyl-pregna-4,17(20)c-dien-3-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: Dehydrierung durch Septomyxa affinis und anschliessende Acetylierung
2: diacetoxy-phenyl-iodan; OsO4; tert-butyl alcohol / Reagens 4: Pyridin
3: Hydrolysis
View Scheme
21-acetoxy-11β-hydroxy-6α-methyl-pregna-1,4,17(20)c-trien-3-one
1968-76-9

21-acetoxy-11β-hydroxy-6α-methyl-pregna-1,4,17(20)c-trien-3-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: diacetoxy-phenyl-iodan; OsO4; tert-butyl alcohol / Reagens 4: Pyridin
2: Hydrolysis
View Scheme
(20Ξ)-11β-hydroxy-6α-methyl-17,20;20,21-bis-methylenedioxy-pregn-4-en-3-one
123292-91-1

(20Ξ)-11β-hydroxy-6α-methyl-17,20;20,21-bis-methylenedioxy-pregn-4-en-3-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: acetic acid; tert-butyl alcohol; selenium dioxide
2: aqueous formic acid
View Scheme
17α,20;20,21-bismethylenedioxypregn-4-ene-3,11-dione
3607-68-9

17α,20;20,21-bismethylenedioxypregn-4-ene-3,11-dione

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 8 steps
1: benzene; toluene-4-sulfonic acid
2: peroxybenzoic acid; benzene / Behandeln unter Ausschluss von Licht, Behandeln des Reaktionsprodukts mit Ameisensaeure und Erwaermen des danach isolierten Reaktionsprodukts mit wss.-methanol. Kalilauge
3: toluene-4-sulfonic acid
4: benzene; diethyl ether
5: pyridine; thionyl chloride / Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether und Benzol
6: acetone; toluene-4-sulfonic acid
7: acetic acid; tert-butyl alcohol; selenium dioxide
8: aqueous formic acid
View Scheme
(20Ξ)-17,20;20,21-bis-methylenedioxy-5α-pregnane-3,6,11-trione
55701-21-8

(20Ξ)-17,20;20,21-bis-methylenedioxy-5α-pregnane-3,6,11-trione

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: toluene-4-sulfonic acid
2: benzene; diethyl ether
3: pyridine; thionyl chloride / Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether und Benzol
4: acetone; toluene-4-sulfonic acid
5: acetic acid; tert-butyl alcohol; selenium dioxide
6: aqueous formic acid
View Scheme
(20Ξ)-3,3-ethanediyldioxy-6-methyl-17,20;20,21-bis-methylenedioxy-pregn-5-en-11β-ol

(20Ξ)-3,3-ethanediyldioxy-6-methyl-17,20;20,21-bis-methylenedioxy-pregn-5-en-11β-ol

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetone; toluene-4-sulfonic acid
2: acetic acid; tert-butyl alcohol; selenium dioxide
3: aqueous formic acid
View Scheme
6-methyl-11-oxo-3-pyrrolidino-pregna-3,5,17(20)c-trien-21-oic acid methyl ester
1968-77-0

6-methyl-11-oxo-3-pyrrolidino-pregna-3,5,17(20)c-trien-21-oic acid methyl ester

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: LiAlH4; diethyl ether / Behandeln des Reaktionsprodukts mit wss.-methanol.Alkalilauge
2: Dehydrierung durch Septomyxa affinis und anschliessende Acetylierung
3: diacetoxy-phenyl-iodan; OsO4; tert-butyl alcohol / Reagens 4: Pyridin
4: Hydrolysis
View Scheme
(8′S,9′S,10′R,13′S,14′S,17′R)-10′,13′-dimethyl-1′,2′,4′,7′,8′,9′,10′,12′,13′,14′,15′,16′-dodecahydro-11′H-trispiro[[1,3]dioxolane-2,3′-cyclopenta[a]phenanthrene-17′,4''-[1,3]dioxolane-5'',4'''-[1,3]dioxolan]-11′-one
52248-40-5

(8′S,9′S,10′R,13′S,14′S,17′R)-10′,13′-dimethyl-1′,2′,4′,7′,8′,9′,10′,12′,13′,14′,15′,16′-dodecahydro-11′H-trispiro[[1,3]dioxolane-2,3′-cyclopenta[a]phenanthrene-17′,4''-[1,3]dioxolane-5'',4'''-[1,3]dioxolan]-11′-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1: peroxybenzoic acid; benzene / Behandeln unter Ausschluss von Licht, Behandeln des Reaktionsprodukts mit Ameisensaeure und Erwaermen des danach isolierten Reaktionsprodukts mit wss.-methanol. Kalilauge
2: toluene-4-sulfonic acid
3: benzene; diethyl ether
4: pyridine; thionyl chloride / Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether und Benzol
5: acetone; toluene-4-sulfonic acid
6: acetic acid; tert-butyl alcohol; selenium dioxide
7: aqueous formic acid
View Scheme
(20Ξ)-3,3-ethanediyldioxy-6β-hydroxy-6α-methyl-17,20;20,21-bis-methylenedioxy-5α-pregnan-11-one
123885-50-7

(20Ξ)-3,3-ethanediyldioxy-6β-hydroxy-6α-methyl-17,20;20,21-bis-methylenedioxy-5α-pregnan-11-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: pyridine; thionyl chloride / Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether und Benzol
2: acetone; toluene-4-sulfonic acid
3: acetic acid; tert-butyl alcohol; selenium dioxide
4: aqueous formic acid
View Scheme
(20Ξ)-3,3-ethanediyldioxy-17,20;20,21-bis-methylenedioxy-5α-pregnane-6,11-dione
107157-45-9

(20Ξ)-3,3-ethanediyldioxy-17,20;20,21-bis-methylenedioxy-5α-pregnane-6,11-dione

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: benzene; diethyl ether
2: pyridine; thionyl chloride / Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether und Benzol
3: acetone; toluene-4-sulfonic acid
4: acetic acid; tert-butyl alcohol; selenium dioxide
5: aqueous formic acid
View Scheme
HYCp45

HYCp45

A

C16H27NO11

C16H27NO11

B

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
With sodium hydroxide In water-d2 at 37℃; pH=7.0;
C26H42O6

C26H42O6

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1.1: sulfuric acid / tetrahydrofuran / pH 2 - 3
2.1: D-glucose; potassium dihydrogenphosphate / water; methanol / 50 h
3.1: iodine; calcium oxide / methanol; dichloromethane
3.2: 2 h / 45 - 50 °C
4.1: potassium hydroxide / methanol; dichloromethane / 0.33 h / 10 - 15 °C / Inert atmosphere
View Scheme
11β,17-dihydroxy-6α-methyl-pregn-4-ene-3,20-dione
7055-53-0

11β,17-dihydroxy-6α-methyl-pregn-4-ene-3,20-dione

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: D-glucose; potassium dihydrogenphosphate / water; methanol / 50 h
2.1: iodine; calcium oxide / methanol; dichloromethane
2.2: 2 h / 45 - 50 °C
3.1: potassium hydroxide / methanol; dichloromethane / 0.33 h / 10 - 15 °C / Inert atmosphere
View Scheme
17-hydroxy-pregn-4-ene-3,11,20-trione
1882-82-2

17-hydroxy-pregn-4-ene-3,11,20-trione

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 8 steps
1.1: trimethyloxosulfonium bromide; orthoformic acid triethyl ester / 5 h
2.1: sodium tetrahydroborate / tetrahydrofuran / 12 h
3.1: phthalic anhydride; dihydrogen peroxide / ethyl acetate / 6 h
4.1: magnesium / tetrahydrofuran / 4 h
5.1: sulfuric acid / tetrahydrofuran / pH 2 - 3
6.1: D-glucose; potassium dihydrogenphosphate / water; methanol / 50 h
7.1: iodine; calcium oxide / methanol; dichloromethane
7.2: 2 h / 45 - 50 °C
8.1: potassium hydroxide / methanol; dichloromethane / 0.33 h / 10 - 15 °C / Inert atmosphere
View Scheme
3,3;20,20-bis-ethanediyldioxy-17-hydroxy-pregn-5-en-11-one
74332-34-6

3,3;20,20-bis-ethanediyldioxy-17-hydroxy-pregn-5-en-11-one

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1.1: sodium tetrahydroborate / tetrahydrofuran / 12 h
2.1: phthalic anhydride; dihydrogen peroxide / ethyl acetate / 6 h
3.1: magnesium / tetrahydrofuran / 4 h
4.1: sulfuric acid / tetrahydrofuran / pH 2 - 3
5.1: D-glucose; potassium dihydrogenphosphate / water; methanol / 50 h
6.1: iodine; calcium oxide / methanol; dichloromethane
6.2: 2 h / 45 - 50 °C
7.1: potassium hydroxide / methanol; dichloromethane / 0.33 h / 10 - 15 °C / Inert atmosphere
View Scheme
3,3;20,20-bis-ethanediyldioxy-pregn-5-ene-11β,17-diol
41870-77-3

3,3;20,20-bis-ethanediyldioxy-pregn-5-ene-11β,17-diol

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1.1: phthalic anhydride; dihydrogen peroxide / ethyl acetate / 6 h
2.1: magnesium / tetrahydrofuran / 4 h
3.1: sulfuric acid / tetrahydrofuran / pH 2 - 3
4.1: D-glucose; potassium dihydrogenphosphate / water; methanol / 50 h
5.1: iodine; calcium oxide / methanol; dichloromethane
5.2: 2 h / 45 - 50 °C
6.1: potassium hydroxide / methanol; dichloromethane / 0.33 h / 10 - 15 °C / Inert atmosphere
View Scheme
C25H38O7

C25H38O7

Methylprednisolone
83-43-2

Methylprednisolone

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: magnesium / tetrahydrofuran / 4 h
2.1: sulfuric acid / tetrahydrofuran / pH 2 - 3
3.1: D-glucose; potassium dihydrogenphosphate / water; methanol / 50 h
4.1: iodine; calcium oxide / methanol; dichloromethane
4.2: 2 h / 45 - 50 °C
5.1: potassium hydroxide / methanol; dichloromethane / 0.33 h / 10 - 15 °C / Inert atmosphere
View Scheme
Methylprednisolone
83-43-2

Methylprednisolone

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

2-((6S,8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-6,10,13-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl methanesulfonate
51474-81-8

2-((6S,8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-6,10,13-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl methanesulfonate

Conditions
ConditionsYield
With pyridine at 0 - 10℃;95%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃;81%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃;
ethyl orthoacetate
58924-88-2

ethyl orthoacetate

Methylprednisolone
83-43-2

Methylprednisolone

A

6α-methylprednisolone 17α,21-ethyl orthoacetate

6α-methylprednisolone 17α,21-ethyl orthoacetate

B

17α,21-diacetoxy-11β-hydroxy-6α-methyl-1,4-pregnadiene-3,20-dione
86413-24-3

17α,21-diacetoxy-11β-hydroxy-6α-methyl-1,4-pregnadiene-3,20-dione

Conditions
ConditionsYield
With sodium carbonate; toluene-4-sulfonic acid In N-methyl-acetamide; water; ethyl acetateA 92.5%
B n/a
methyl orthovalerate
856317-97-0

methyl orthovalerate

Methylprednisolone
83-43-2

Methylprednisolone

A

6α-methylprednisolone 17α,21-methyl orthovalerate

6α-methylprednisolone 17α,21-methyl orthovalerate

B

11β,21-dihydroxy-6α-methyl-17α-valeroyloxy-1,4-pregnadiene-3,20-dione
86413-38-9

11β,21-dihydroxy-6α-methyl-17α-valeroyloxy-1,4-pregnadiene-3,20-dione

Conditions
ConditionsYield
With sodium carbonate; toluene-4-sulfonic acid In N-methyl-acetamide; water; ethyl acetateA n/a
B 91.7%
methyl orthoisovalerate

methyl orthoisovalerate

Methylprednisolone
83-43-2

Methylprednisolone

A

6α-methylprednisolone 17α,21-methyl orthoisovalerate

6α-methylprednisolone 17α,21-methyl orthoisovalerate

B

11β,21-dihydroxy-17α-isovaleryloxy-6α-methyl-1,4-pregnadiene-3,20-dione
86413-32-3

11β,21-dihydroxy-17α-isovaleryloxy-6α-methyl-1,4-pregnadiene-3,20-dione

Conditions
ConditionsYield
With sodium carbonate; toluene-4-sulfonic acid In N-methyl-acetamide; water; ethyl acetateA 82.8%
B n/a
3-sulfopropanoic acid
44826-45-1

3-sulfopropanoic acid

Methylprednisolone
83-43-2

Methylprednisolone

21-<<3-sulfo-1-oxopropyl>oxy>-11β,17-dihydroxy-6α-methylpregna-1,4-diene-3,20-dione

21-<<3-sulfo-1-oxopropyl>oxy>-11β,17-dihydroxy-6α-methylpregna-1,4-diene-3,20-dione

Conditions
ConditionsYield
With pyridine; dicyclohexyl-carbodiimide for 16h;70%
Methylprednisolone
83-43-2

Methylprednisolone

17α,21-dihydroxy-6α-methylpregna-1,4-diene-3,11,20-trione
111264-84-7, 91523-05-6

17α,21-dihydroxy-6α-methylpregna-1,4-diene-3,11,20-trione

Conditions
ConditionsYield
With pyridine; N-bromoacetamide
Methylprednisolone
83-43-2

Methylprednisolone

11β,17α-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione
6870-94-6

11β,17α-dihydroxy-6α-methyl-1,4-pregnadiene-3,20-dione

Conditions
ConditionsYield
ueber mehrere Stufen;

Methylprednisolone Consensus Reports

Reported in EPA TSCA Inventory.

Methylprednisolone Specification

1. Introduction of Methylprednisolone
Methylprednisolone is one kind of white to off-white crystalline powder. And its IUPAC name is also called(6S,8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one. It belongs to the classes of Miscellaneous Biochemicals; Biochemistry; Hydroxyketosteroids; Steroids; Intermediates & Fine Chemicals; Pharmaceuticals. It is sparingly soluble in alcohol, in dioxane, and in methanol, slightly soluble in acetone, and in chloroform, and very slightly soluble in ether. It is practically insoluble in water.

The Classification Code of this chemical is Adrenal Cortex Hormones; Anti-Inflammatory Agents; Anti-inflammatory; Antiemetics; Autonomic Agents; Central Nervous System Agents; Drug / Therapeutic Agent; Gastrointestinal Agents; Glucocorticoid; Glucocorticoids; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Human Data; Immunosuppressant; Neuroprotective agents; Peripheral Nervous System Agents; Protective Agents.

2. Properties of Methylprednisolone
Physical properties about Methylprednisolone are:
(1)ACD/LogP: 1.99; (2) # of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.99; (4)ACD/LogD (pH 7.4): 1.99; (5)ACD/BCF (pH 5.5): 19.06; (6)ACD/BCF (pH 7.4): 19.06; (7)ACD/KOC (pH 5.5): 287.01; (8)ACD/KOC (pH 7.4): 287.01; (9)#H bond acceptors: 5; (10)#H bond donors: 3; (11)#Freely Rotating Bonds: 5; (12)Polar Surface Area: 61.83 Å2; (13)Index of Refraction: 1.602; (14)Molar Refractivity: 100.08 cm3; (15)Molar Volume: 291.4 cm3; (16)Surface Tension: 58.1 dyne/cm; (17)Density: 1.28 g/cm3; (18)Flash Point: 313.7 °C; (19)Enthalpy of Vaporization: 98.47 kJ/mol; (20)Boiling Point: 571.8 °C at 760 mmHg; (21)Vapour Pressure: 1.86E-15 mmHg at 25°C; (22)Refractive index: 82 ° (C=1, Dioxane); (23)Melting Point: 228-237°C.

3. Structure Descriptors of Methylprednisolone
You can still convert the following datas into molecular structure:
(1)SMILES: O=C\1\C=C/[C@]4(/C(=C/1)[C@@H](C)C[C@@H]2[C@@H]4[C@@H](O)C[C@@]3([C@@](O)(C(=O)CO)CC[C@@H]23)C)C;
(2)InChI: InChI=1/C22H30O5/c1-12-8-14-15-5-7-22(27,18(26)11-23)21(15,3)10-17(25)19(14)20(2)6-4-13(24)9-16(12)20/h4,6,9,12,14-15,17,19,23,25,27H,5,7-8,10-11H2,1-3H3/t12-,14-,15-,17-,19+,20-,21-,22-/m0/s1;
(3)InChIKey: VHRSUDSXCMQTMA-PJHHCJLFBP
(4)Canonical SMILES : CC1CC2C3CCC(C3(CC(C2C4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O
(5)Isomeric SMILES: C[C@H]1C[C@H]2[C@@H]3CC[C@@]([C@]3(C[C@@H]([C@@H]2[C@@]4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O

4. Toxicity of Methylprednisolone
The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 2292mg/kg (2292mg/kg)   Drugs in Japan Vol. 6, Pg. 832, 1982.
rat LD50 oral > 4gm/kg (4000mg/kg)   Drugs in Japan Vol. 6, Pg. 832, 1982.
women TDLo intravenous 20mg/kg/45M-C (20mg/kg) CARDIAC: ARRHYTHMIAS (INCLUDING CHANGES IN CONDUCTION) Journal of Rheumatology. Vol. 13, Pg. 477, 1986.
women TDLo intravenous 60mg/kg/3D-I (60mg/kg) CARDIAC: PULSE RATE INCREASE WITHOUT FALL IN BP

VASCULAR: BP LOWERING NOT CHARACTERIZED IN AUTONOMIC SECTION
Annals of Internal Medicine. Vol. 99, Pg. 282, 1983.
women TDLo parenteral 2400ug/kg (2.4mg/kg) CARDIAC: CHANGE IN RATE

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION
British Journal of Anesthesia. Vol. 69, Pg. 422, 1992.

5. Physical Properties of Methylprednisolone

Physical Property Value Units Temp (deg C) Source
Melting Point 232.5 deg C   EXP
log P (octanol-water) 1.820 (none)   EST
Water Solubility 120 mg/L 25 EXP
Atmospheric OH Rate Constant 7.39E-11 cm3/molecule-sec 25 EST

6. Uses of Methylprednisolone
this chemical can be used as a glucocorticoid. And it is used for rheumatoid arthritis, collagen diseases, allergic disease, ophthalmic disease, lymphatic leukemia, soft tissue inflammation and hemolytic anemia. It can be used for Bio-Research.

7. Safety information of Methylprednisolone
Hazard Codes: XiXi
Risk Statements: 36/37/38
36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 22-36-26
22: Do not breathe dust.
36: Wear suitable protective clothing.
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 2
RTECS: TU4146000
F: 8-10-23
When you are using this chemical, please be cautious about it as the following:
Moderately toxic by intraperitoneal route. A steroid hormone. Human systemic effects include arrhythmias, blood pressure lowering, heart rate changes, increased body temperature, pulse rate increase, respiratory depression. When heated to decomposition it emits acrid smoke and irritating fumes. Wear suitable protective clothing, gloves and eye/face protection when you are using it. Do not breathe dust. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. Store it at temperature of 0-6°C.

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