Cas no 78821-43-9 (Epibrassinolide)

Epibrassinolide is a plant hormone with potent biological activities. It exhibits strong antifungal and antibacterial properties, making it valuable in agricultural applications. This compound is highly effective in promoting plant growth and enhancing crop yield, while being safe for the environment. Its unique structure allows for optimal bioavailability, ensuring consistent and reliable performance in various agricultural settings.
Epibrassinolide structure
Epibrassinolide structure
Product Name:Epibrassinolide
CAS No:78821-43-9
MF:C28H48O6
MW:480.677129745483
MDL:MFCD00133310
CID:60034
PubChem ID:24894426
Update Time:2025-06-24

Epibrassinolide Chemical and Physical Properties

Names and Identifiers

    • epibrassinolide
    • Brassinolide
    • 24-Epibrassinolide
    • 24-Epicastasterone
    • 24-epi-brassinolide
    • .(22R,23R,24R)-2
    • 24-(R)-EPIBRASSINOLIDE
    • 3.24-EPIBRASSINOLIDE
    • 4-Epicastasterone
    • B1105
    • BP55
    • BRASSINOLIDE(BR)
    • Brassinolide(epibrassinolide,Homobrassinolide)
    • CH09964 EPIBRASSINOLIDE
    • Epibrassinolide(24-Epibrassinolide)
    • 22R,23R,24R-2α,3α,22,23-Tetrahydroxy-B-homo-7-oxa-5α-ergostan-6-one
    • 22R,23R,24R-2a,3a,22,23-Tetrahydroxy-B-homo-7-oxa-5a-ergostan-6-one
    • CHOLESTAN-6-ONE DERIV
    • NSC325611
    • NSC325306
    • Epibrassinolide R
    • 10-(3,4-dihydroxy-5,6-dimethylheptan-2-yl)-5,6-dihydroxy-7a,9a-dimethylhexadecahydro-3h-benzo[c]indeno[5,4-e]oxepin-3-one
    • 5-Chloro-2-[(5R)-5-methyl-4-[5-methyl-2-(2H-1,2,3-triazol-2-y
    • (1S,2R,4R,5S,7S,11S,12S,15R,16S)-15-[(2S,3R,4R,5R)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-4,5-dihydroxy-2,16-dimethyl-9-oxatetracyclo[9.7.0.02,7.012,16]octadecan-8-one
    • Epibrassinolide, >=85%
    • 24(R)-Epibrassinolide
    • Q27103283
    • 78821-43-9
    • 3H-Benz[c]indeno[5,4-e]oxepin-3-one, 10-[(1S,2R,3R,4R)-2,3-dihydroxy-1,4,5-trimethylhexyl]hexadecahydro-5,6-dihydroxy-7a,9a-dimethyl-, (3aS,5S,6R,7aR,7bS,9aS,10R,12aS,12bS)-
    • CHEMBL563853
    • (22R,23R,24R)-2alpha,3alpha,22,23-Tetrahydroxy-b-homo-7-oxa-5alpha-ergostan-6-one
    • 2,3,22,23-Tetrahydroxy-24-methyl-B-homo-7-oxacholestan-6-one
    • 1ST40091
    • HY-N0848
    • Sunergist ebr
    • UNII-49CN25465Y
    • CHEBI:27722
    • 49CN25465Y
    • SCHEMBL1614884
    • B-HOMO-7-OXAERGOSTAN-6-ONE, 2,3,22,23-TETRAHYDROXY-, (2.ALPHA.,3.ALPHA.,5.ALPHA.,22R,23R)-
    • 6H-Benz(C)indeno(5,4-E)oxepin-6-one, 1-(2,3-dihydroxy-1,4,5-trimethylhexyl)hexadecahydro-8,9-dihydroxy-10a,12a-dimethyl-, (1R-(1alpha(1S*,2R*,3R*,4R*),3abeta,3balpha,6abeta,8beta,9beta,10aalpha,10bbeta,12aalpha))-
    • (1R,3aS,3bS,6aS,8S,9R,10aR,10bS,12aS)-1-((1S,2R,3R,4R)-2,3-Dihydroxy-1,4,5-trimethylhexyl)hexadecahydro-8,9-dihydroxy-10a,12a-dimethyl-6H-benz(C)indeno(5,4-E)oxepin-6-one
    • AKOS027250811
    • (22R,23R)-2alpha,3alpha,22,23-tetrahydroxy-7a-homo-7-oxa-5alpha-ergostan-6-one
    • Brassin lactone
    • LMST01140002
    • B-1105
    • CS-3129
    • AS-76479
    • Epi Brassinolide, 90%
    • B-HOMO-7-oxaergostan-6-one, 2,3,22,23-tetrahydroxy-, (2alpha,3alpha,5alpha,22R,23R)-
    • MFCD00133310
    • 6H-BENZ(C)INDENO(5,4-E)OXEPIN-6-ONE, 1-(2,3-DIHYDROXY-1,4,5-TRIMETHYLHEXYL)HEXADECAHYDRO-8,9-DIHYDROXY-10A,12A-DIMETHYL-, (1R-(1.ALPHA.(1S*,2R*,3R*,4R*),3A.BETA.,3B.ALPHA.,6A.BETA.,8.BETA.,9.BETA.,10A.ALPHA.,10B.BETA.,12A.ALPHA.))-
    • (22R,23R,24R)-2.ALPHA.,3.ALPHA.,22,23-TETRAHYDROXY-B-HOMO-7-OXA-5.ALPHA.-ERGOSTAN-6-ONE
    • s8870
    • 24-Epibrassinolide;B1105;BP55
    • (1R,3aS,3bS,6aS,8S,9R,10aR,10bS,12aS)-1-[(1S,2R,3R,4R)-2,3-Dihydroxy-1,4,5-trimethylhexyl]hexadecahydro-8,9-dihydroxy-10a,12a-dimethyl-6H-benz[c]indeno[5,4-e]oxepin-6-one (ACI)
    • B-Homo-7-oxaergostan-6-one, 2,3,22,23-tetrahydroxy-, (2α,3α,5α,22R,23R)- (ZCI)
    • (22R,23R,24R)-2α,3α,22,23-Tetrahydroxy-B-homo-7-oxa-5α-ergostan-6-one
    • 6H-Benz[c]indeno[5,4-e]oxepin-6-one, 1-(2,3-dihydroxy-1,4,5-trimethylhexyl)hexadecahydro-8,9-dihydroxy-10a,12a-dimethyl-, [1R-[1α(1S*,2R*,3R*,4R*),3aβ,3bα,6aβ,8β,9β,10aα,10bβ,12aα]]-
    • B 1105
    • BP 55
    • Epin
    • DA-52938
    • 24-Epi Brassinolide, 90%
    • 72962-43-7
    • IXVMHGVQKLDRKH-QHBHMFGVSA-N
    • DTXSID10705357
    • Epibrassinolide
    • MDL: MFCD00133310
    • Inchi: 1S/C28H48O6/c1-14(2)15(3)24(31)25(32)16(4)18-7-8-19-17-13-34-26(33)21-11-22(29)23(30)12-28(21,6)20(17)9-10-27(18,19)5/h14-25,29-32H,7-13H2,1-6H3/t15-,16+,17+,18-,19+,20+,21-,22+,23-,24-,25-,27-,28-/m1/s1
    • InChI Key: IXVMHGVQKLDRKH-QHBHMFGVSA-N
    • SMILES: C[C@@]12[C@@H]([C@H](C)[C@@H](O)[C@H](O)[C@H](C)C(C)C)CC[C@H]1[C@@H]1COC(=O)[C@H]3C[C@@H]([C@@H](C[C@]3(C)[C@H]1CC2)O)O

Computed Properties

  • Exact Mass: 480.34500
  • Monoisotopic Mass: 480.345
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 34
  • Rotatable Bond Count: 5
  • Complexity: 755
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 13
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 107
  • Molecular Weight: 480.7
  • XLogP3: 4.8

Experimental Properties

  • Density: 1.141
  • Melting Point: 256 oC
  • Boiling Point: 633.7 oC at 760 mmHg
  • Flash Point: 633.7 oC at 760 mmHg
  • Refractive Index: 1.535
  • PSA: 107.22000
  • LogP: 3.39000

Epibrassinolide Security Information

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Epibrassinolide Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Trifluoroacetic anhydride ,  Hydrogen peroxide Solvents: Chloroform ,  Water
Reference
Improved synthesis of 24-epibrassinolide from ergosterol
McMorris, Trevor C.; Patil, Prakash A., Journal of Organic Chemistry, 1993, 58(8), 2338-9

Production Method 2

Reaction Conditions
1.1 Reagents: 2,2,2-Trifluoroethaneperoxoic acid Solvents: Dichloromethane ,  Water ;  3 h, 0 °C
Reference
The Baeyer-Villiger oxidation of ketones and aldehydes
Krow, Grant R., Organic Reactions (Hoboken, 1993, 43,

Production Method 3

Reaction Conditions
1.1 Reagents: 2,2,2-Trifluoroethaneperoxoic acid Solvents: Dichloromethane
Reference
Steroids. Part CCCLXXIII. New method of preparation of brassinosteroids
Kohout, Ladislav, Collection of Czechoslovak Chemical Communications, 1994, 59(2), 457-60

Production Method 4

Reaction Conditions
1.1 Reagents: Trifluoroacetic acid Solvents: Methyl chloride
Reference
Biological Activity of Brassinosteroids - Direct Comparison of Known and New Analogs in planta
Wendeborn, Sebastian; Lachia, Mathilde; Jung, Pierre M. J.; Leipner, Joerg; Brocklehurst, David; et al, Helvetica Chimica Acta, 2017, 100(2),

Production Method 5

Reaction Conditions
1.1 Reagents: Hydrogen peroxide Solvents: Trifluoroacetic anhydride
Reference
The improved synthesis of epibrassinolide and its application in agriculture
Cheprakov, A. V.; Filatov, M. A.; Lukashev, N. V.; Beletskaya, I. P.; Malevannaya, N. N., Biotechnology, 2006, 41, 41-45

Production Method 6

Reaction Conditions
1.1 Reagents: 2,2,2-Trifluoroethaneperoxoic acid Solvents: Dichloromethane
Reference
Preparation of brassinosteroids
, Czech Republic, , ,

Epibrassinolide Raw materials

Epibrassinolide Preparation Products

Epibrassinolide Suppliers

Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
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(CAS:78821-43-9)24-Epi Brassinolide
Order Number:LE12043;LE8405338
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:06
Price ($):discuss personally
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Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:78821-43-9)24-Epi Brassinolide
LE12043;LE8405338
Purity:99%/99%
Quantity:25KG,200KG,1000KG/25KG,200KG,1000KG
Price ($):Inquiry/Inquiry
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