1-Bromobutane

1-Bromobutane Basic information
Product Name:1-Bromobutane
Synonyms:N-BUTYL BROMIDE;BUTYL BROMIDE;1-Brombutan;1-bromo-butan;1-BROMOBUTANE;1-BroMobutane, Reagent;1-BroMobutane, 98+%, 98+%;1-bromobutane/ butyl bromide
CAS:109-65-9
MF:C4H9Br
MW:137.02
EINECS:203-691-9
Product Categories:Pharmaceutical Intermediates;Organics;ALKYL BROMIDE;Bromine Compounds;Alkyl Bromides;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes;Dyestuff Intermediates
Mol File:109-65-9.mol
1-Bromobutane Structure
1-Bromobutane Chemical Properties
Melting point -112 °C
Boiling point 100-104 °C(lit.)
density 1.276 g/mL at 25 °C(lit.)
vapor density 4.7 (vs air)
vapor pressure 150 mm Hg ( 50 °C)
refractive index n20/D 1.439(lit.)
Fp 23 °C
storage temp. Store below +30°C.
solubility 0.6g/l
form Liquid
color Clear colorless to light yellow
Odorcharacteristic odor
explosive limit2.8-6.6%, 100°F
Water Solubility 0.608 g/L (30 ºC)
Merck 14,1553
BRN 1098260
Stability:Stable. Flammable - note low flash point. Incompatible with strong oxidizing agents, strong bases.
InChIKeyMPPPKRYCTPRNTB-UHFFFAOYSA-N
LogP2.75
CAS DataBase Reference109-65-9(CAS DataBase Reference)
NIST Chemistry ReferenceButane, 1-bromo-(109-65-9)
EPA Substance Registry System1-Bromobutane (109-65-9)
Safety Information
Hazard Codes F,Xi,N
Risk Statements 11-36/37/38-51/53-10
Safety Statements 16-26-60-37/39
RIDADR UN 1126 3/PG 2
WGK Germany 2
RTECS EJ6225000
Autoignition Temperature509 °F
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29033036
Hazardous Substances Data109-65-9(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 2761 mg/kg
MSDS Information
ProviderLanguage
1-Bromobutane English
SigmaAldrich English
ACROS English
ALFA English
1-Bromobutane Usage And Synthesis
Chemical Properties1-bromobutane appears as a clear colorless to slightly yellow liquid with aroma. Flash point 65°F. Denser than water and insoluble in water, soluble in organic solvents such as alcohol, ether and chloroform.Vapors heavier than air.
Uses1-Bromobutane is used as an intermediate in organic synthesis and as a solvent for cleaning and degreasing. It acts as an alkylating agent as well as to prepare organometallic compounds such as n-butyllithium. It is also involved in the synthesis of procaine and tetracaine. It reacts with magnesium metal to prepare the Grignard reagent, which is used to form carbon-carbon bonds.
Application1-Bromobutane may be used as a derivatization reagent for multiple functional groups (amino, carboxyl, and phenolic hydroxyl groups) of amino acids to improve hydrophobicities and basicities of the amino acids. It may also be used as an internal standard for the quantification of 1- and 2-bromopropane in human urine by headspace gas chromatography.
Synthesis Reference(s)Journal of the American Chemical Society, 86, p. 964, 1964 DOI: 10.1021/ja01059a073
Organic Syntheses, Coll. Vol. 1, p. 25, 1941
Synthesis, p. 326, 1982
General Description1-Bromobutane, an alkyl halide, is an alkylating agent. Its rotational constants, nuclear quadrupole constants and centrifugal distortion constants have been stated based on microwave spectral data. The rate coefficient for the reaction of 1-bromobutane with hydrogen atoms has been reported to be 2.4±1.2x1010cm3mol-1s-1.
Air & Water ReactionsHighly flammable. Insoluble in water.
Reactivity Profile1-Bromobutane is incompatible with strong bases and oxidizers [USCG, 1999].
HazardFlammable, dangerous fire risk.
Health HazardIrritating to the eyes, nose, throat, and upper respiratory tract. Symptoms of exposure include burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea, and vomiting. Irritating to the skin.
Safety ProfileModerately toxic by intraperitoneal route. Mddly toxic by inhalation. Dangerous fire hazard when exposed to heat, flame, or oxidizers. Violent reaction with bromobenzene + sodium above 30℃. Can react with oxidizing materials. To fight fire, use CO2, dry chemical, mist or spray. See also BROMIDES.
Synthesis1-bromobutane is a primary alkyl halide (primary alkyl) and therefore it is produced from bimolecular nucleophilic substitution reactions (Sn2).
The preparation method of 1-bromobutane is as follows: stirring n-butanol, sodium bromide, water and sulfuric acid evenly, heating under reflux for 3 hours, steaming out the crude bromobutane, washing with water, treating with cold concentrated sulfuric acid, and distilling to obtain the finished product.
Reaction equation: CH3CH2CH2CH2OH+NaBr+H2SO4→CH3CH2CH2CH2Br+Na2SO4+H2O
This halide is easily prepared by reacting butan-1-ol (primary alcohol) with sodium bromide solution and excess of concentrated sulfuric acid. The reaction between sodium bromide and sulphuric acid origins hydrobromic acid.
ShippingUN1126 & UN23391- & 2-Bromobutane, Hazard Class: 3; Labels: 3—Flammable liquid.
Purification MethodsWash the bromide with conc H2SO4, water, 10% Na2CO3 and again with H2O. Dry it over CaCl2, CaSO4 or K2CO3, and distil it. Redistil it after drying with P2O5, or pass it through two columns containing 5:1 silica gel/Celite mixture and store it with freshly activated alumina. [Beilstein 1 IV 258.]
IncompatibilitiesVapor may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. May accumulate static electrical charges and cause ignition of its vapors.
Waste DisposalDissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed
2-Bromo-2-methylpropane BROMOBUTANE, 2-,2-BROMOBUTANE,BROMOBUTANE, 2-(SG),2-Bromobutane,98%,2-Bromobutane, 99+%,2-Bromobutane sec-Butylbromide,2-BROMOBUTANE,REAGENT 1-Chloro-2-methylpropane 1,4-Dibromopentane Cyhalofop-butyl Rocuronium bromide 1-Bromobutane Vecuronium bromide ISOBUTANE Buprofezin Dimidium bromide n-Butane Sodium bromate Ethidium bromide 1,4-Dibromobutane 2-BROMOTRIDECANE Allyl bromide Methyl bromide

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.