trans-2,3-Dibromo-2-butene-1,4-diol
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trans-2,3-Dibromo-2-butene-1,4-diol
structure -
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CAS No:
3234-02-4
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Formula:
C4H6Br2O2
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Chemical Name:
trans-2,3-Dibromo-2-butene-1,4-diol
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Synonyms:
2,3-dibromo-2-butene-4-diol;4-diol,2,3-dibromo-2-Butene-1;TRANS-2,3-DIBROMO-1,4-DIHYDROXY-2-BUTENE;TRANS-2,3-DIBROMO-2-BUTENE-1,4-DIOL;TRANS-2,3-DIBROMO-2-BUTEN-1,4-DIOL;DBD;DIBROMO(-2,3)-2-BUTENE-1,4-DIOL;2,3-DIBROMO-2-BUTYLENE-1,4-DIOL
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CAS No:
Description
white crystalline powder
Crystals or white powder. (NTP, 1992)
Crystals or white powder. (NTP, 1992)
trans-2,3-Dibromo-2-butene-1,4-diol Basic Attributes
245.9
245.90
221-779-5
W297831A99
76595
TSCA listed
DTXSID3024942|DTXSID90274233
29055998
Characteristics
40.5
2.70
Crystals or white powder. (NTP, 1992)
1.9671 (rough estimate)
112-114 °C(lit.)
318.1±42.0 °C(Predicted)
146.2±27.9 °C
1.5230 (estimate)
1-5 g/100 mL at 21 ºC
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
0.004-0.081Pa at 25-40℃
11.91±0.10(Predicted)
Water soluble.
Alcohols and Polyols
A halogenated alkene and alcohol. The unsaturated aliphatic hydrocarbons are generally much more reactive than the alkanes, which are saturated aliphatic hydrocarbons. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. 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.
Storage temp. 2-8°C
Safety Information
I; II; III
6.1
NONH for all modes of transport
3
Xi
26-37/39
EM6910000
Xi
Irritant
Stable. Incompatible with strong oxidizing agents.
P201, P202, P281, P308+P313, P405, P501
36/37/38
Flash point data for trans-2,3-Dibromo-2-butene-1,4-diol are not available, however trans-2,3-Dibromo-2-butene-1,4-diol is probably combustible.
|Warning|H317 (95.24%): May cause an allergic skin reaction [Warning Sensitization, Skin]|P261, P272, P280, P302+P352, P321, P333+P313, P363, and P501|Aggregated GHS information provided by 42 companies from 3 notifications to the ECHA C&L Inventory.|H341 (100%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]|P201, P202, P281, P308+P313, P405, and P501|Aggregated GHS information provided by 2 companies from 1 notifications to the ECHA C&L Inventory.
Fires involving this compound can be controlled using a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, you should dampen the solid spill material with alcohol, then transfer the dampened material to a suitable container. Use absorbent paper dampened with alcohol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution. Do not reenter the contaminate 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 an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)
Drug Information
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. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. 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. (NTP, 1992)
dibromobutenediol
trans-2,3-Dibromo-2-butene-1,4-diol Use and Manufacturing
This product has no pollution, low toxicity and no frost. It is a high-temperature initiating high-efficiency plasticizer. It is suitable for high-temperature dense mixing and is added when starting plasticizing. The processing temperature should be above 120℃. The dosage in NR rubber is about 0.1-0.15%, and the dosage in styrene-butadiene rubber should be increased appropriately.
Synthesis and Characterization of Oligomer Bis (trans-2, 3-dibromo-4-hydroxy-2-butenyl) terephthalate as a Green Corrosion Inhibitor on Mild Steel in 1 MH 3 PO 4:This study discusses the conversion of PET waste into an oligomer using trans-2,3-dibromo-2-butene-1,4-diol, exploring its efficacy as a corrosion inhibitor (Tuama, Indonesian Journal of Chemistry).Use of bromine and bromo-organic compounds in organic synthesis:This review highlights the role of trans-2,3-dibromo-2-butene-1,4-diol in organic synthesis, particularly its utility in bromination reactions to synthesize complex organic molecules (Saikia et al., Chemical Reviews, 2016).
2-Butene-1,4-diol, 2,3-dibromo-: ACTIVE
Computed Properties
Molecular Weight:245.90
XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:245.87141
Monoisotopic Mass:243.87345
Topological Polar Surface Area:40.5
Heavy Atom Count:8
Complexity:88.2
Defined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of trans-2,3-Dibromo-2-butene-1,4-diol
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CN
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trans-2,3-Dibromo-2-butene-1,4-diol
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