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· · COA & SDS available for every product · Same-day shipping on in-stock items Phorbol - 10mM in DMSO , CAS No.17673-25-5
GRADE & PURITY 10mM in DMSO
Synonyms
AC-33956 | (1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-4a,7b,9,9a-tetrahydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-1,1a,1b,4,4a,7a,7b,8,9,9a-decahydro-5H-cyclopropa[3,4]benzo[1,2-e]azulen-5-one | (1S,2S,6R,10S,11R,13S,14R,15R)-1,6,13,14-tetrahydroxy-8-(hydroxymethy
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Phorbol is a plant-derived diterpene that is a tumor promoter through the activation of protein kinase C.
Specifications Synonyms
AC-33956 | (1aR, 1bS, 4aR, 7aS, 7bS, 8R, 9R, 9aS)-4a, 7b, 9, 9a-tetrahydroxy-3-(hydroxymethyl)-1, 1, 6, 8-tetramethyl-1, 1a, 1b, 4, 4a, 7a, 7b, 8, 9, 9a-decahydro-5H-cyclopropa[3, 4]benzo[1, 2-e]azulen-5-one | (1S, 2S, 6R, 10S, 11R, 13S, 14R, 15R)-1, 6, 13, 14-tetrahydroxy-8-(hydroxymethy
Specifications & Purity
10mM in DMSO
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4(CC(=C3)CO)O)C)O)O)O IUPAC Name (1S,2S,6R,10S,11R,13S,14R,15R)-1,6,13,14-tetrahydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyltetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dien-5-one InChIKey QGVLYPPODPLXMB-UBTYZVCOSA-N INCHI 1S/C20H28O6/c1-9-5-13-18(24,15(9)22)7-11(8-21)6-12-14-17(3,4)20(14,26)16(23)10(2)19(12,13)25/h5-6,10,12-14,16,21,23-26H,7-8H2,1-4H3/t10-,12+,13-,14-,16-,18-,19-,20-/m1/s1 Isomeric SMILES C[C@@H]1[C@H]([C@@]2([C@@H](C2(C)C)[C@H]3[C@]1([C@@H]4C=C(C(=O)[C@]4(CC(=C3)CO)O)C)O)O)O RTECS GZ0600000 UN Number 2811 Packing Group I Molecular Weight 364.43 Reaxy-Rn 41521892 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=41521892&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Lipids and lipid-like molecules Class Prenol lipids Subclass Diterpenoids Intermediate Tree Nodes Not available Direct Parent Tigliane and ingenane diterpenoids Alternative Parents Tertiary alcohols Secondary alcohols Ketones Cyclic alcohols and derivatives Polyols Primary alcohols Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic homopolycyclic compounds Substituents Tigliane diterpenoid - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Ketone - Cyclopropanol - Polyol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as tigliane and ingenane diterpenoids. These are diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane. External Descriptors Tigliane and ingenane diterpenoids Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Heat sensitive Specific Rotation[α] α20/D 102°, c = 1 in water; α20/D 118°, c = 0.4 in dioxane Boil Point(°C) 572° C at 760 mmHg (Predicted) Melt Point(°C) 250-251° C Molecular Weight 364.400 g/mol XLogP3 -0.800 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 1 Exact Mass 364.189 Da Monoisotopic Mass 364.189 Da Topological Polar Surface Area 118.000 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 753.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 8 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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