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Home > Encyclopedia > Mitobronitol

Mitobronitol

pharmaceutical raw materials
Mitobronitol structure

Mitobronitol 

structure
  • CAS No:

    488-41-5

  • Formula:

    C6H12Br2O4

  • Chemical Name:

    Mitobronitol

  • Synonyms:

    D-Mannitol,1,6-dibromo-1,6-dideoxy-;Mannitol,1,6-dibromo-1,6-dideoxy-,D-;1,6-Dibromo-1,6-dideoxy-D-mannitol;DBM;Myelobromol;1,6-Dibromomannitol;1,6-Dibromo-1,6-dideoxymannitol;1,6-Dibromo-D-mannitol;Mitobronitol;1,6-Dideoxy-1,6-dibromo-D-mannitol;Mielobromol;Myebrol;NSC 94110;D-Dibromomannitol;NCI C04762;Dibromannit;Dibromomannitol;NSC 94100;Dibromannitol;R 54;1,6-Dibromo-1,6-dideoxy-d-mannitol;33375-11-0;478243-88-8

  • Categories:

    Active Pharmaceutical Ingredients  >  Antineoplastic Agents

Description

PHYSICAL DESCRIPTION: White powder. (NTP, 1992)


Dibromomannitol is a white powder. (NTP, 1992)


Dibromomannitol is a white powder. (NTP, 1992)|Brominated analog of MANNITOL which is an antineoplastic agent appearing to act as an alkylating agent.

Mitobronitol Basic Attributes

307.97

307.97

207-676-8

616232|140389|104800|94100|240600

DTXSID7022918

L - Antineoplastic and immunomodulating agents

2905590090

Characteristics

80.9

-0.3

Dibromomannitol is a white powder. (NTP, 1992)

2.03 g/cm3

176-178 °C

511.2ºC at 760mmHg

263ºC

1.622

less than 1 mg/mL at 68° F (NTP, 1992)

−20°C

Insoluble in water.

Alcohols and Polyols

A halogenated alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Safety Information

3

45-22

53-22-36/37/39-45

OP2800000

T

P201, P202, P264, P270, P281, P301+P312, P308+P313, P330, P405, P501

H302

Flash point data for this compound are not available, but it is probably combustible. (NTP, 1992)

Fires involving this chemical should be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)

SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. STORAGE PRECAUTIONS: You should store this material in a refrigerator. (NTP, 1992)

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with a combination filter cartridge, i.e. organic vapor/acid gas/HEPA (specific for organic vapors, HCl, acid gas, SO2 and a high efficiency particulate filter). (NTP, 1992)

Drug Information

A class of drugs that differs from other alkylating agents used clinically in that they are monofunctional and thus unable to cross-link cellular macromolecules. Among their common properties are a requirement for metabolic activation to intermediates with antitumor efficacy and the presence in their chemical structures of N-methyl groups, that after metabolism, can covalently modify cellular DNA. The precise mechanisms by which each of these drugs acts to kill tumor cells are not completely understood. (From AMA, Drug Evaluations Annual, 1994, p2026) (See all compounds classified as Antineoplastic Agents, Alkylating.)

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. IMMEDIATELY call a physician and be prepared to transport the victim to a hospital even if no symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. OTHER: Since this chemical is a known or suspected carcinogen you should contact a physician for advice regarding the possible long term health effects and potential recommendation for medical monitoring. Recommendations from the physician will depend upon the specific compound, its chemical, physical and toxicity properties, the exposure level, length of exposure, and the route of exposure. (NTP, 1992)

Dibromomannitol

Mitobronitol Use and Manufacturing

Antineoplastic.

Computed Properties

Molecular Weight:307.96
XLogP3:-0.3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:307.90818
Monoisotopic Mass:305.91023
Topological Polar Surface Area:80.9
Heavy Atom Count:12
Complexity:110
Undefined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

No specific pharmacological effects mentioned

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Beijing Saier Biological Pharmaceutical Co., Ltd.

    China China
    Active

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