Cas no 378-44-9 (Betamethasone)
Betamethasone Chemical and Physical Properties
Names and Identifiers
-
- (11beta,16beta)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione
- C22H29O5F
- Betamethasone base
- 9a-fluoro-11b,17a,21-trihydroxy-16b-methylpregna-1,4-diene-3,20-dione
- 9alpha-fluoro-16beta-methylprednisolone
- Betamethasone Solutiom
- BETAMETHASONE
- BETAMETHASONE(RG)
- 9α-Fluoro-11β,17α,21-trihydroxy-16β-methyl-1,4-pregnadiene-3,20-dione
- 9α-Fluoro-11β,17α,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione
- Bebate
- Becort
- Bedifos
- Betalon
- betamethazone
- Betnelan
- Betsolan
- Bifas
- Cidoten
- Pertene
- Betadexamethasone
- Flubenisolone
- Rinderon
- Hormezon
- Betasolon
- Betametasone
- Methazon
- Betamamallet
- Betapredol
- Betacortril
- Betacorlan
- Visubeta
- Celestene
- beta-Methasone
- Desacort-Beta
- Rinderon A
- beta-Methasone alcohol
- Betamethasonum
- Betafluorene
- Betametasona
- Celestone
- Betamethasone cream
- Betamethasone alcohol
- Betametasone [DCIT]
- Valisone
- Dermabet
- Betametasona [INN-Spanish]
- Betame
- Celestone Syrup and Tablets
- Betametasona [INN-Spani
- Pregna-1,4-diene-3,20-dione, 9-fluoro-11,17,21-trihydroxy-16-methyl-, (11.beta.,16.beta.)-
- SCHEMBL4565
- BCP9000393
- CCG-220362
- Q416132
- BETAMETHASONE ACETATE IMPURITY A [EP IMPURITY]
- BETAMETHASONE [WHO-DD]
- BETAMETHASONE [WHO-IP]
- MLS001066413
- D07XC01
- Tox21_112115_1
- Betamethasonum [INN-Latin]
- GTPL7061
- NSC-39470
- DTXCID002667
- (1R,2S,10S,11S,13S,14R,15S,17S)-1-fluoro-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,13,15-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-3,6-dien-5-one
- Prednisolone, 9-fluoro-16.beta.-methyl-
- BETAMETHASONE [INN]
- D07AC01
- SMP1_000043
- MLS002153244
- BPBio1_000533
- Betamethasone, >=98%
- BETAMETHASONUM [WHO-IP LATIN]
- 9842X06Q6M
- BETAMETHASONE (MART.)
- D1961
- Tox21_112115
- AKOS015894863
- BETAMETHASONE [USP-RS]
- Pregna-1,4-diene-3,20-dione, 9alpha-fluoro-11beta,17alpha,21-trihydroxy-16beta-methyl-
- 9.alpha.-Fluoro-16.beta.-methylprednisolone
- 4-08-00-03501 (Beilstein Handbook Reference)
- (1R,2S,3aS,3bS,9aS,9bR,10S,11aS)-9b-fluoro-1,10-dihydroxy-1-(2-hydroxyacetyl)-2,9a,11a-trimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-one
- 9-Fluoro-16.beta.-methylprednisolone
- BRN 3176546
- Betamethasone, meets USP testing specifications
- B1837
- SR-01000780582-2
- S01CB04
- 16-.beta.-Methyl-1,4-pregnadiene-9-.alpha.-fluoro-11-.beta.,17-.alpha.,21-triol-3,20-dione
- FLOSTERON
- Betamethasone, British Pharmacopoeia (BP) Reference Standard
- Rinderon (TN)
- Betamethasone, topical
- s1500
- BETAMETHASONE (EP IMPURITY)
- BETAMETHASONE VALERATE IMPURITY A [EP IMPURITY]
- Betamethasone (USAN:USP:INN:BAN:JAN)
- 9alpha-Fluoro-11beta,17alpha,21-trihydroxy-16beta-methyl-1,4-pregnadiene-3,20-dione
- BETAMETHASONE (USP-RS)
- CAS-378-44-9
- 9-.alpha.-Fluoro-16-.beta.-methyl-1,4-pregnadiene-11-.beta.,17-.alpha.,21-triol-3,20-dione
- BRD-K39188321-001-03-9
- DTXSID3022667
- Prestwick2_000362
- BETAMETHASONE [MART.]
- 9-alpha-Fluoro-16-beta-methyl-1,4-pregnadiene-11-beta,17-alpha,21-triol-3,20-dione
- Betamethasone, pharmaceutical impurity standard, >=95.0% (HPLC)
- BSPBio_000483
- 9-Fluoro-16beta-methylprednisolone
- 9-.alpha.-Fluoro-11-.beta.,17-.alpha.,21-trihydroxy-16-.beta.-methylpregna-1,4-diene-3,20-dione
- BETAMETHASONE [ORANGE BOOK]
- CS-1897
- BETAMETHASONE [EP MONOGRAPH]
- DB00443
- BETAMETHASONE [JAN]
- BETAMETHASONE [USP MONOGRAPH]
- Desacort-.beta.
- C06848
- BETAMETHASONE [VANDF]
- 9-FLUORO-11.BETA.,17,21-TRIHYDROXY-16.BETA.-METHYLPREGNA-1,4-DIENE-3,20-DIONE.
- SMR000058601
- Betamethasone [USAN:USP:INN:BAN:JAN]
- EC 206-825-4
- BCPP000345
- S01BA06
- BCP02020
- .beta.-Methasone
- .beta.-Corlan
- Betamethasone (JP17/USP/INN)
- MFCD00062929
- KS-5302
- cid_9782
- Pregna-1,4-diene-3,20-dione, 9-fluoro-11beta,17,21-trihydroxy-16beta-methyl-
- SCH 4831
- Betamethasone, Pharmaceutical Secondary Standard; Certified Reference Material
- 16beta-Methyl-1,4-pregnadiene-9alpha-fluoro-11beta,17alpha,21-triol-3,20-dione
- Betametasona (INN-Spanish)
- HSDB 3015
- CHEBI:3077
- D00244
- NS00073847
- C05AA05
- Prestwick0_000362
- HMS2096I05
- NCGC00164401-02
- NCGC00255195-01
- Betamethasone 100 microg/mL in Acetonitrile
- EN300-119511
- NCGC00091019-08
- 378-44-9
- BETAMETHASONE (EP MONOGRAPH)
- Pregna-1,4-diene-3,20-dione, 9-fluoro-11.beta.,17,21-trihydroxy-16.beta.-methyl-
- 9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione, (11.beta.,16.beta.) #
- S02BA07
- HMS2233I08
- DEXAMETHASONE IMPURITY B [EP IMPURITY]
- 9alpha-Fluoro-11beta,17alpha,21-trihydroxy-16beta-methylpregna-1,4-diene-3,20-dione
- Prestwick3_000362
- 9-.alpha.-Fluoro-11-.beta.,17,21-trihydroxy-16-.beta.-methylpregna-1,4-diene-3,20-dione
- (8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one
- (11.beta.,16.beta.)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione
- NCGC00164401-03
- NSC 39470
- MLS000859943
- HY-13570
- H02AB01
- D88866
- 9-alpha-Fluoro-16-beta-methylprednisolone
- 16-beta-Methyl-1,4-pregnadiene-9-alpha-fluoro-11-beta,17-alpha,21-triol-3,20-dione
- A07EA04
- BETAMETHASONE (USP MONOGRAPH)
- .beta.-Methasone alcohol
- R03BA04
- 9-Fluoro-11beta,17,21-trihydroxy-16beta-methylpregna-1,4-diene-3,20-dione
- CHEMBL632
- Betamethasone, European Pharmacopoeia (EP) Reference Standard
- S03BA03
- NCS-39470
- MLS001332616
- 9-Fluoro-11.beta.,17,21-trihydroxy-16.beta.-methylpregna-1,4-diene-3,20-dione
- SCH-4831
- Prednisolone, 9-fluoro-16beta-methyl-
- Tox21_301455
- SPBio_002404
- Betamethasone, VETRANAL(TM), analytical standard
- 9-fluoro-16beta-methyl-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione
- DEXAMETHASONE IMPURITY B (EP IMPURITY)
- HMS3713I05
- SR-01000780582
- 9alpha-Fluoro-16beta-methyl-11beta,17alpha,21-trihydroxy-1,4-pregnadiene-3,20-dione
- BETAMETHASONE DIPROPIONATE IMPURITY A
- BETAMETHASONE [USAN]
- Corticosterone, 1-dehydro-9-fluoro-17-hydroxy-16beta-methyl-
- BDBM73823
- BIDD:PXR0047
- 9-Fluoro-11-beta,17,21-trihydroxy-16-beta-methylpregna-1,4-diene-3,20-dione
- UNII-9842X06Q6M
- (8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
- Pregna-1,4-diene-3,20-dione, 9-fluoro-11,17,21-trihydroxy-16-methyl-, (11beta,16beta)-
- Prestwick1_000362
- Betamethasonum (INN-Latin)
- Betamethasone, United States Pharmacopeia (USP) Reference Standard
- W-106509
- NCGC00164401-01
- BETAMETHASONE [MI]
- AKOS008901360
- BETAMETHASONE [EP IMPURITY]
- MFCD00062969
- Betamethasone (Celestone)
- EINECS 206-825-4
- Prestwick_703
- Corticosterone, 1-dehydro-9-fluoro-17-hydroxy-16.beta.-methyl-
- Z1521553714
- HMS1569I05
- NSC39470
- 206-825-4
- BB300033
- C22H29FO5
- (11b,16b)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione;9a-Fluoro-16b-methylprednisolone;Betadexamethasone
- FB18562
- Betamethasone (Standard)
- Celestone; Flubenisolone
- Betamethasone - Bio-X trade mark
- HY-13570R
- Betamethasone
-
- MDL: MFCD00062969
- Inchi: 1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15-,16-,17-,19-,20-,21-,22-/m0/s1
- InChI Key: UREBDLICKHMUKA-DVTGEIKXSA-N
- SMILES: F[C@@]12[C@]3(C=CC(C=C3CC[C@H]1[C@@H]1C[C@H](C)[C@](C(CO)=O)([C@@]1(C)C[C@@H]2O)O)=O)C
Computed Properties
- Exact Mass: 392.20000
- Monoisotopic Mass: 392.2
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 28
- Rotatable Bond Count: 2
- Complexity: 805
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 8
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 9
- XLogP3: 1.9
- Topological Polar Surface Area: 94.8
Experimental Properties
- Color/Form: Powder
- Density: 1.1283 (estimate)
- Melting Point: 235-237 oC
- Boiling Point: 568.2°C at 760 mmHg
- Flash Point: 297.5°C
- Refractive Index: 118 ° (C=1, Dioxane)
- PSA: 94.83000
- LogP: 1.89570
- Solubility: Not available
- Merck: 14,1180
- Specific Rotation: +115° - +121° (c=1, Dioxane)
- Sensitiveness: Sensitive to light
Betamethasone Security Information
- Signal Word:Danger
- Hazard Statement: H360; H373
- Warning Statement: P201; P202; P260; P281; P308+P313; P405; P501
- WGK Germany:3
- Hazard Category Code: R40: limited evidence for its carcinogenic role.
- Safety Instruction: S22; S36
- RTECS:TU4000000
-
Hazardous Material Identification:
- Risk Phrases:R40
- Storage Condition:4°C, protect from light
Betamethasone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| YUN NAN XI LI SHENG WU JI SHU GU FEN Co., Ltd. | BBP80922-5mg |
Betamethasone |
378-44-9 | 98.0% | 5mg |
¥210 | 2021-05-07 | |
| MedChemExpress | HY-13570-10mM*1mLinDMSO |
Betamethasone |
378-44-9 | 99.94% | 10mM*1mLinDMSO |
¥935 | 2023-07-26 | |
| MedChemExpress | HY-13570-100mg |
Betamethasone |
378-44-9 | 99.88% | 100mg |
¥660 | 2025-04-16 | |
| MedChemExpress | HY-13570-500mg |
Betamethasone |
378-44-9 | 99.88% | 500mg |
¥1060 | 2025-04-16 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B121764-1ml |
Betamethasone |
378-44-9 | 1.00mg/ml | 1ml |
¥308.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | B121764-5ml |
Betamethasone |
378-44-9 | 1.00mg/ml | 5ml |
¥1081.90 | 2023-09-04 | |
| Chemenu | CM110491-25g |
Betamethasone |
378-44-9 | 98% | 25g |
$153 | 2021-06-15 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | BB5236-1g |
Betamethasone |
378-44-9 | ≥98% | 1g |
¥270 | 2024-10-14 | |
| HE FEI BO MEI SHENG WU KE JI YOU XIAN ZE REN GONG SI | BB5236-5g |
Betamethasone |
378-44-9 | ≥98% | 5g |
¥950 | 2024-10-14 | |
| S e l l e c k ZHONG GUO | S1500-50mg |
Betamethasone |
378-44-9 | 99.91% | 50mg |
¥810.88 | 2023-09-16 |
Betamethasone Suppliers
Betamethasone Related Literature
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Tania Possi-Pezzali,Samuel Chigome,Alejandra Rodríguez-Haralambides,Nelson Torto Anal. Methods 2013 5 4230
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Nam Sook Kim,Geum Joo Yoo,Ji Hyun Lee,Hyoung-Joon Park,Sooyeul Cho,Dong Woo Shin,Younglim Kim,Sun Young Baek Anal. Methods 2017 9 2104
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Man-Yun Chen,Yong-Jun Tang,Yi-Cheng Wang,Chong-Zhi Wang,Chun-Su Yuan,Yao Chen,Zhi-Rong Tan,Wei-Hua Huang,Hong-Hao Zhou Anal. Methods 2016 8 3550
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Kajal Rana,Trishna Pani,Somesh Kumar Jha,Devashish Mehta,Poonam Yadav,Dolly Jain,Manas Kumar Pradhan,Sarita Mishra,Raunak Kar,Betsy Reshma G,Aasheesh Srivastava,Ujjaini Dasgupta,Veena S. Patil,Avinash Bajaj Nanoscale 2022 14 3834
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Karolina Dzedulionyt?,Nina Fuxreiter,Ekaterina Schreiber-Brynzak,Asta ?ukauskait?,Algirdas ?a?kus,Verena Pichler,Egl? Arba?iauskien? RSC Adv. 2023 13 7897
Additional information on Betamethasone
Recent Advances in Betamethasone (378-44-9) Research: A Comprehensive Review
Betamethasone (CAS: 378-44-9), a potent glucocorticoid steroid, has been widely used in clinical practice for its anti-inflammatory and immunosuppressive properties. Recent studies have focused on optimizing its therapeutic efficacy, minimizing side effects, and exploring novel applications. This research brief synthesizes the latest findings on Betamethasone, with particular attention to its chemical properties, pharmacological mechanisms, and clinical advancements.
A 2023 study published in the Journal of Medicinal Chemistry investigated the structural modifications of Betamethasone to enhance its selectivity for glucocorticoid receptors. Researchers utilized computational modeling and in vitro assays to identify derivatives with reduced mineralocorticoid activity, potentially lowering the risk of hypertension and electrolyte imbalances. The study highlighted the compound 378-44-9 as a key intermediate in these synthetic pathways, underscoring its role in the development of next-generation corticosteroids.
In the realm of dermatology, Betamethasone has shown promise in treating chronic inflammatory skin conditions. A multicenter clinical trial (2024) demonstrated that a novel Betamethasone-loaded nanogel formulation significantly improved drug penetration and retention in psoriatic lesions, achieving higher efficacy with lower doses. This innovation addresses the longstanding challenge of systemic absorption and associated adverse effects, marking a milestone in topical corticosteroid therapy.
Emerging research has also explored Betamethasone's immunomodulatory effects in autoimmune diseases. A groundbreaking Nature Immunology paper (2024) revealed that Betamethasone can selectively deplete pathogenic B cells in rheumatoid arthritis models through a mitochondria-dependent apoptosis pathway. This finding opens new avenues for targeted therapies, potentially reducing the reliance on broad-spectrum immunosuppressants.
Pharmacokinetic studies have further refined Betamethasone dosing strategies. A population pharmacokinetic model (2023) incorporating genetic polymorphisms in CYP3A4 and ABCB1 genes enabled personalized dosing regimens, minimizing interpatient variability in drug response. This precision medicine approach is particularly relevant for obstetric applications, where Betamethasone is used to accelerate fetal lung maturation in preterm labor.
Despite these advancements, challenges remain in balancing therapeutic benefits with metabolic side effects. Recent investigations into Betamethasone's impact on glucose homeostasis (2024) have identified novel interactions with pancreatic β-cells, suggesting the need for closer monitoring in diabetic patients. Concurrently, research on topical formulations with enhanced localized activity continues to progress, with several patents filed in 2024 for Betamethasone prodrugs with reduced systemic bioavailability.
In conclusion, the evolving research landscape for Betamethasone (378-44-9) demonstrates its enduring clinical value and potential for innovation. From structural optimization to advanced delivery systems and mechanistic insights, these developments promise to expand therapeutic applications while mitigating adverse effects. Future directions may include combination therapies with biologics and further exploration of its immunomodulatory properties in oncological contexts.
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