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Home > Biochemical Engineering > Chinese Herbs > 10-Deacetylbaccatin III for Sale > BEST QUALITY SUPPLYER MOST PROFESSIONAL 10-Deacetylbaccatin III (32981-86-5) IN bulk
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BEST QUALITY SUPPLYER MOST PROFESSIONAL 10-Deacetylbaccatin III (32981-86-5) IN bulk

Unit Price: Get Latest Price
CAS No.:

32981-86-5

Grade:

Pharmaceutical Grade

Content:

99%

Port:

Durban

Brand:

Custom

Packaging:

As per customer requirement

Price valid (until):

2024-05-27

Company Type:
Distributor
Location:
South Africa
Qualification:
Main Products:

Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

  • Product Description

  • Seller Information

  • Description


      Product Detail  


                                                                                      1. Chemical Structure: 10-Deacetylbaccatin III is a natural product, a precursor of paclitaxel (Taxol), which is a well-known anticancer drug. It is a complex diterpenoid compound with a molecular formula of C29H36O10.

                                                                                      2. Isolation: 10-Deacetylbaccatin III is isolated from the needles of the Taxus species, primarily Taxus baccata (European yew) and Taxus brevifolia (Pacific yew), as well as other Taxus species.

                                                                                      3. Biological Importance: It plays a crucial role as a precursor in the semi-synthesis of paclitaxel, a potent chemotherapy medication used to treat various cancers, including breast, ovarian, and lung cancers.

                                                                                      4. Chemical Transformation: Through chemical synthesis or semi-synthesis, 10-Deacetylbaccatin III can be converted into paclitaxel by acetylation at the C10 position, leading to the formation of the key pharmacophore of paclitaxel.

                                                                                      5. Medicinal Uses: While 10-Deacetylbaccatin III itself is not used directly as a medication, its conversion into paclitaxel makes it invaluable in the pharmaceutical industry for the production of paclitaxel-based chemotherapy drugs.

                                                                                      6. Anticancer Activity: Paclitaxel, derived from 10-Deacetylbaccatin III, acts by stabilizing microtubules in cancer cells, preventing their breakdown during cell division, and ultimately leading to cell death. This mechanism makes paclitaxel highly effective against rapidly dividing cancer cells.

                                                                                      7. Semi-Synthesis of Paclitaxel: The semi-synthesis of paclitaxel from 10-Deacetylbaccatin III involves several chemical steps, including acetylation at the C10 position, oxidation of the C9 position, and other modifications to yield the final product.

                                                                                      8. Pharmaceutical Importance: Paclitaxel and its derivatives, produced from 10-Deacetylbaccatin III, are among the most widely used chemotherapy agents worldwide and are essential in the treatment of various types of cancer.

                                                                                      9. Research and Development: Ongoing research is focused on developing more efficient and sustainable methods for the production of paclitaxel and its derivatives from 10-Deacetylbaccatin III, as well as exploring its potential in the treatment of other diseases.

                                                                                      10. Natural Source: The Taxus species, from which 10-Deacetylbaccatin III is obtained, are cultivated or harvested for their bark, leaves, and needles, which contain valuable compounds used in cancer treatment and research.

                                                                                      11. Chemical Characterization: The structure of 10-Deacetylbaccatin III has been elucidated through various spectroscopic techniques, including nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.

                                                                                      12. Synthetic Biology: Advances in synthetic biology and genetic engineering have enabled the production of 10-Deacetylbaccatin III and its derivatives through microbial fermentation or plant cell culture, providing alternative sources for its production.

                                                                                      13. Market Demand: Given the significant demand for paclitaxel and its derivatives in the pharmaceutical industry, 10-Deacetylbaccatin III remains a valuable natural product with a substantial market value.

                                                                                      14. Regulatory Considerations: The production and use of 10-Deacetylbaccatin III and its derivatives are subject to regulatory oversight by health authorities to ensure their safety, efficacy, and quality in pharmaceutical applications.

                                                                                      15. Future Prospects: As research continues to unravel the therapeutic potential of paclitaxel and explore new avenues for its use in cancer treatment and other diseases, the importance of 10-Deacetylbaccatin III as a precursor will likely continue to grow, driving further innovation in drug development and production processes.

    Items Specifications
    Chemical Name 10-Deacetylbaccatin III
    CAS Number 32981-86-5
    Chemical Formula C29H36O10
    Molecular Weight 544.59 g/mol
    Appearance White to off-white crystalline powder
    Odor Odorless
    Melting Point 235-237°C
    Boiling Point Not available
    Solubility in Water Insoluble
    Solubility in Organic Solvents Soluble in organic solvents such as methanol, ethanol, chloroform, and acetone
    pH (aqueous solution) Not applicable
    Density Not available
    Flash Point Not applicable
    Storage Conditions Store in a cool, dry place away from heat and light. Keep container tightly closed. Protect from moisture.
    Biological Sources 10-Deacetylbaccatin III is a naturally occurring taxane diterpenoid compound found in the needles of various species of yew trees, particularly Taxus baccata, Taxus brevifolia, and Taxus cuspidata.
    Pharmacological Uses 10-Deacetylbaccatin III is a precursor in the semi-synthesis of paclitaxel (Taxol), a widely used anticancer medication. It is used as a starting material in the pharmaceutical industry for the synthesis of paclitaxel and other taxane-based anticancer drugs.
    Commercial Preparations 10-Deacetylbaccatin III is primarily used as an intermediate in the synthesis of paclitaxel (Taxol) and other taxane-based pharmaceuticals. It is not typically available as a standalone medication or dietary supplement.


      Product Detail  


    Shop High Quality 99% Purity of 10-Deacetylbaccatin III CAS NO 32981-86-5-Detailed Image 1Shop High Quality 99% Purity of 10-Deacetylbaccatin III CAS NO 32981-86-5-Detailed Image 2Shop High Quality 99% Purity of 10-Deacetylbaccatin III CAS NO 32981-86-5-Detailed Image 3Shop High Quality 99% Purity of 10-Deacetylbaccatin III CAS NO 32981-86-5-Detailed Image 4Shop High Quality 99% Purity of 10-Deacetylbaccatin III CAS NO 32981-86-5-Detailed Image 5Shop High Quality 99% Purity of 10-Deacetylbaccatin III CAS NO 32981-86-5-Detailed Image 6

    Basic Info
    Product Name:

    10-Deacetylbaccatin III

    Other Name:

    7,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one,12b-(acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dodecahydro-4,6,9,11-tetrahydroxy-4a,8,13,13-tetramethyl-,(2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-;Tax-11-en-9-one,5β,20-epoxy-1,2α,4,7β,10β,13α-hexahydroxy-,4-acetate 2-benzoate;7,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one,12b-(acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dodecahydro-4,6,9,11-tetrahydroxy-4a,8,13,13-tetramethyl-,[2aR-(2aα,4β,4aβ,6β,9α,11α,12α,12aα,12bα)]-;(2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-12b-(Acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dodecahydro-4,6,9,11-tetrahydroxy-4a,8,13,13-tetramethyl-7,11-methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one;10-Deacetylbaccatin III;10-Desacetylbaccatin III;NSC 251677;10β-Deacetylbaccatin III;10-Deacetylbaccatin;115509-92-7

    CAS No.:

    32981-86-5

    Molecular Formula:

    C29H36O10

    InChIKeys:

    InChIKey=YWLXLRUDGLRYDR-ZHPRIASZSA-N

    Molecular Weight:

    544.59

    Exact Mass:

    544.59

    EC Number:

    418-680-6

    NSC Number:

    251677

    HScode:

    29329990

    Categories:

    Chinese Herbs

    Characteristics
    PSA:

    160

    XLogP3:

    1.08180

    Appearance:

    white Powder

    Density:

    1.2007 (rough estimate)

    Melting Point:

    221-223 °C @ Solvent: Ethanol

    Boiling Point:

    717℃

    Flash Point:

    >110°(230°F)

    Refractive Index:

    1.624

    Water Solubility:

    H2O: INsoluble ;methanol: soluble , clear, colorless (5 mg + 0.1 mL MeOH)

    Storage Conditions:

    2-8°C

    Specific rotation:

    -44.5 º (c=1, methanol 25 ºC)

    Hazard Identification

    Classification of the substance or mixture

    Skin irritation, Category 2

    Eye irritation, Category 2

    Germ cell mutagenicity, Category 1B

    Carcinogenicity, Category 1A

    Specific target organ toxicity – repeated exposure, Category 2

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Danger

    Hazard statement(s)

    H315 Causes skin irritation

    H319 Causes serious eye irritation

    H335 May cause respiratory irritation

    H340 May cause genetic defects

    H350 May cause cancer

    H373 May cause damage to organs through prolonged or repeated exposure

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    P203 Obtain, read and follow all safety instructions before use.

    P260 Do not breathe dust/fume/gas/mist/vapours/spray.

    Response

    P302+P352 IF ON SKIN: Wash with plenty of water/...

    P321 Specific treatment (see ... on this label).

    P332+P317 If skin irritation occurs: Get medical help.

    P362+P364 Take off contaminated clothing and wash it before reuse.

    P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

    P318 IF exposed or concerned, get medical advice.

    P319 Get medical help if you feel unwell.

    Storage

    P405 Store locked up.

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Distributor

    Main Products:

    Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

    Location:

    13 PROTEA PARK MILKWOOD STREET RANGEVIEW GAUTENG 1739

    Payment Terms:

    TT against copy of documents,TT against B/L draft before shipment

    Average lead Time:

    60

    Total Annual Revenue:

    $1 million-$2.5 million

    Total Employees:

    11-50

    Year of Establishment:

    2012

  • Country Product Purchase Quantity Date Posted
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