Bromoacetic acid 79...

Bromoacetic acid 79-08-3

Bromoacetic acid 79-08-3

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1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99.00%
  • Payment Terms : T/T,Other

Keywords

79-08-3 Bromoacetic acid alpha-Bromoethanoic acid

Quick Details

  • Appearance:WHITE TO LIGHT YELLOW CRYSTALLINE MASS
  • Application:intermediate
  • PackAge:drums
  • ProductionCapacity:100|Metric Ton|Month
  • Storage:dry and cool
  • Transportation:air, courier and sea

Superiority:

Synonyms: Aceticacid,bromo-;Acide bromacetique;acidebromacetique;alpha-Bromoethanoic acid;alpha-bromoethanoicacid;Bromaceticacid;bromoacetateion;bromoacetic
CAS: 79-08-3
MF: C2H3BrO2
MW: 138.95
EINECS: 201-175-8
Product Categories: Pharmaceutical Intermediates;Aliphatics;Carboxylic Acids;ACID BASED BROMO COMPOUNDS;omega-Bromocarboxylic Acids;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;Carboxylic Acids;500 Series Drinking Water Methods;BromoEPA;Chemical Class;Method 552;C1 to C5Chemical Synthesis;Carbonyl Compounds;A-BChemical Class;Organic AcidsEssential Chemicals;Reagent Grade;Routine Reagents;A-BAlphabetic;Alpha Sort;B;BI - BZChemical Class;Bromo;Halogenated;Volatiles/ Semivolatiles;Chemical Synthesis;Organic Acids;Synthetic Reagents;acid
Mol File: 79-08-3.mol
Bromoacetic acid Structure
Bromoacetic acid Chemical Properties
Melting point  46-49 °C
Boiling point  208 °C(lit.)
density  1
Fp  >110°C
storage temp.  0-6°C
Water Solubility  miscible
Sensitive  Light Sensitive & Hygroscopic
Merck  14,1400
BRN  506167
CAS DataBase Reference 79-08-3(CAS DataBase Reference)
NIST Chemistry Reference Acetic acid, bromo-(79-08-3)
EPA Substance Registry System Acetic acid, bromo-(79-08-3)
Safety Information
Hazard Codes  T,C,N,Xi,F
Risk Statements  23/24/25-35-50-40-36/37/38-43-38
Safety Statements  26-36/37/39-45-61-36-16
RIDADR  UN 3425 8/PG 2
WGK Germany  2
RTECS  AF5950000
F  3-19-23
Hazard Note  Toxic/Corrosive
TSCA  Yes
HazardClass  8
PackingGroup  II
Hazardous Substances Data 79-08-3(Hazardous Substances Data)

Details:

Chemical Properties WHITE TO LIGHT YELLOW CRYSTALLINE MASS
General Description Aqueous solution.
Air & Water Reactions Water soluble.
Reactivity Profile Carboxylic acids, such as BROMOACETIC ACID, donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Bromoacetic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
Health Hazard TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Contact with molten substance may cause severe burns to skin and eyes. Reaction with water or moist air will release toxic, corrosive or flammable gases. Reaction with water may generate much heat that will increase the concentration of fumes in the air. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
Fire Hazard Combustible material: may burn but does not ignite readily. Substance will react with water (some violently) releasing flammable, toxic or corrosive gases and runoff. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapors may travel to source of ignition and flash back. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water.
Bromoacetic acid Preparation Products And Raw materials
Preparation Products Ethyl bromoacetate-->Thianaphthene-->Rhodanine-3-acetic acid-->7-HYDROXY-4-METHYL-3-COUMARINYLACETIC ACID-->2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE-->2-Ethylpyrimidine-5-carbaldehyde-->2-METHOXY-PYRIMIDINE-5-CARBALDEHYDE-->2-Amino-5-pyrimidinecarboxyaldehyde-->Methyl bromoacetate-->Ziprasidone-->TRI-TERT-BUTYL 1 4 7 10-TETRAAZACYCLODOD-->Sevoflurane-->PYRROLIDIN-1-YL-ACETIC ACID-->Bromoacetyl chloride
Raw materials Bromine-->Acetic anhydride

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