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Home > Products >  Carboplatin

Carboplatin CAS NO.41575-94-4

  • Min.Order: 10 Gram
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Keywords

  • Carboplatin
  • 41575-94-4
  • C6H12N2O4Pt

Quick Details

  • ProName: Carboplatin
  • CasNo: 41575-94-4
  • Molecular Formula: C6H12N2O4Pt
  • Appearance: White crystal
  • Application: Pharmaceutical
  • DeliveryTime: within 3-7 day
  • PackAge: As required
  • Port: shanghai or other
  • ProductionCapacity: 5 Metric Ton/Month
  • Purity: 99%
  • Storage: keep in dry and cool condition
  • Transportation: by sea or by air
  • LimitNum: 10 Gram

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Details

Carboplatin Basic information
Description References
Product Name: Carboplatin
Synonyms: cbdca;cis-(1,1-cyclobutanedicarboxylato)diammineplatinum(ii);diammine-1,1-cyclobutanedicarboxylateplatinumi;nsc-241240;SP-4-2)-Diammine[1,1-cyclobutanedicar-boxylato-(2-)O,O’]platinum;cis-(1,1-cyclobutanedicarboxylato)diammineplatinum;diammine(1,1-cyclobutanedicarboxylato)platinum;1,1-CYCLOBUTANEDICARBOXYLATODIAMMINEPLATINUM(II) CARBOPLATIN
CAS: 41575-94-4
MF: C6H12N2O4Pt
MW: 371.25
EINECS: 255-446-0
Product Categories: -;Pharmaceutical material and intermeidates;Active Pharmaceutical Ingredients;Antitumors for Research and Experimental Use;Biochemistry;Classes of Metal Compounds;Cyclobutanes & Cyclobutenes;Pt (Platinum) Compounds;Simple 4-Membered Ring Compounds;Transition Metal Compounds;Intermediates & Fine Chemicals;Pharmaceuticals;anti-cancer;metal-ammine complexes;Inhibitors;API;NEMAZINE;Anti cancer;Anti can
Mol File: 41575-94-4.mol
Carboplatin Structure
 
Carboplatin Chemical Properties
Melting point  228-230°C
storage temp.  Store at RT
solubility  Sparingly soluble in water, very slightly soluble in acetone and in ethanol (96 per cent).
form  crystal
color  white
Water Solubility  Soluble in water.
Merck  14,1822
Stability: Stable. Incompatible with strong oxidizing agents.
EPA Substance Registry System Platinum, diammine[1,1-cyclobutanedi( carboxylato-.kappa.O)(2-)]-, (SP-4-2)-(41575-94-4)
 
Safety Information
Hazard Codes  T
Risk Statements  46-61-20/21/22-42/43-20/21
Safety Statements  53-22-26-36/37/39-45
RIDADR  2811
WGK Germany  3
RTECS  TP2300000
HS Code  28439000
Hazardous Substances Data 41575-94-4(Hazardous Substances Data)
Toxicity LD50 in mice (mg/kg): 150 i.p., 140 i.v.; in rats (mg/kg): 85 i.v. (Lelieveld)
Carboplatin Usage And Synthesis
Description Carboplatin (Brand name: Paraplatin) is a kind of chemotherapy medication used for the treatment of a series of cancers. It can be used for the treatment of various kinds of cancers including ovarian cancer, lung cancer, head and neck cancer, brain cancer, and neuroblastoma. Moreover, it may also be used for treating some types of testicular cancer. Carboplatin belongs to a kind of alkylating agent. It takes effect through three major mechanisms: (1) Attach the alkyl groups to the DNA bases, further causing DNA fragmentation so that DNA replication is inhibited; (2) Cause DNA damage through inducing the formation of cross-links which prevents DNA from being separated for synthesis or transcription; (3) Induce mispairing of the nucleotides leading to mutations.
References #
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Description Carboplatin is a second generation, platinum-containing antineoplastic agent with significantly reduced nephro-, neuro-, and ototoxicity in comparison to cisplatin. It is effective in the treatment of advanced ovarian carcinoma of epithelial origin and small cell carcinoma of the lung.
Chemical Properties White Crystals
Originator Johnson Matthey (United Kingdom)
Uses anthelmintic
Uses antitumor agent,
Uses Analog of Cisplatin with reduced nephrotoxicity. Antineoplastic
Indications Carboplatin (Paraplatin) is an analogue of cisplatin. Its plasma half-life is 3 to 5 hours, and it has no significant protein binding. Renal excretion is the major route of drug elimination.
Despite its lower chemical reactivity, carboplatin has antitumor activity that is similar to that of cisplatin against ovarian carcinomas, small cell lung cancers, and germ cell cancers of the testis. Most tumors that are resistant to cisplatin are cross-resistant to carboplatin.
The major advantage of carboplatin over cisplatin is a markedly reduced risk of toxicity to the kidneys, peripheral nerves, and hearing; additionally, it produces less nausea and vomiting. It is, however, more myelosuppressive than cisplatin. Other adverse effects include anemia, abnormal liver function tests, and occasional allergic reactions.
Brand name Paraplatin (Bristol-Myers Squibb).
General Description Carboplatin is available in 50-, 150-, and 450-mg vials for IVadministration in the treatment of ovarian cancer, bladdercancer, germ cell tumors, head and neck cancers, small celllung cancer, and NSCLC. Activation of the agent occurs byaquation in a manner similar to that seen for cisplatin. Thepresence of the chelating 1,1-cyclobutane-dicarboxylateslows this reaction 100-fold and reduces the toxicity of theagent. The sites of alkylation and mechanisms of resistanceare like those seen for cisplatin, and the two agents showcross-resistance. The agent is widely distributed upon IV administration but, because of its greater stability, it bindsslowly to plasma proteins, requiring 24 hours to reach 90%bound drug compared with 4 hours for cisplatin. The agent iseliminated in the urine with a terminal elimination half-lifeof 2 to 6 hours. Adverse effects include myelosuppression,which is dose limiting. Other adverse effects include renaltoxicity, nausea, vomiting, and peripheral neuropathy, butthese occur much less frequently than with cisplatin.
Pharmaceutical Applications Carboplatin, cis-diammine(1,1-cyclobutanedicarboxylato)platinum(II), is a second-generation platinum drug. Its structure is based on cisplatin with the difference that the chloride ligands are exchanged for a bidentate chelating ligand. A consequence is that carboplatin is less reactive than cisplatin and therefore is less nephrotoxic and orthotoxic than the parent compound. Unfortunately, it is more myelosuppressive than cisplatin, which reduces the patients’ white blood cell count and makes them susceptible to infections. Carboplatin was licensed by the FDA in 1989 under the brand name Paraplatin and has since then gained worldwide recognition. Carboplatin on its own or in combination with other anticancer agents is used in the treatment of a variety of cancer types including head and neck, ovarian, small-cell lung, testicular cancer and others.
Carboplatin is a pale-white solid showing good aqueous solubility. The synthesis starts with potassium tetrachloroplatinate, which is reacted to the orange [PtI4]2- anion.
Biological Activity Antitumor agent that forms platinum-DNA adducts. Causes intra- and interstrand DNA crosslinks blocking DNA replication and transcription. Enhances radiation-induced single-strand DNA breakage and displays lower nephrotoxicity than analog cisplatin (cis-Diaminodichloroplatinum ).
Veterinary Drugs and Treatments Like cisplatin, carboplatin may be useful in a variety of veterinary neoplastic diseases including squamous cell carcinomas, ovarian carcinomas, mediastinal carcinomas, pleural adenocarcinomas, nasal carcinomas and thyroid adenocarcinomas. Carboplatin’s primary use currently in small animal medicine is in the adjunctive treatment (post amputation) of osteogenic sarcomas. Its effectiveness in treating transitional cell carcinoma of the bladder has been disappointing; however, carboplatin may have more efficacy against melanomas than does cisplatin.
Carboplatin, unlike cisplatin, appears to be relatively safe to use in cats.
Carboplatin may be considered for intralesional use in conditions such as equine sarcoids or in treating adenocarcinoma in birds.
Whether carboplatin is more efficacious than cisplatin for certain cancers does not appear to be decided at this point, but the drug does appear to have fewer adverse effects (less renal toxicity and reduced vomiting) in dogs.

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