ChemicalBook > Product Catalog >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >Acyclic alcohols >2-Butanol

2-Butanol

2-Butanol Structure
CAS No.
78-92-2
Chemical Name:
2-Butanol
Synonyms
BUTAN-2-OL;SEC-BUTANOL;SEC-BUTYL ALCOHOL;SECONDARY BUTYL ALCOHOL;s-Butanol;Butanol-2;(RS)-2-butanol;S-BUTYL ALCOHOL;1-Methyl propanol;ccs301
CBNumber:
CB0751661
Molecular Formula:
C4H10O
Molecular Weight:
74.12
MOL File:
78-92-2.mol
MSDS File:
SDS
Modify Date:
2024/5/30 16:26:16

2-Butanol Properties

Melting point −115 °C(lit.)
Boiling point 98 °C(lit.)
Density 0.808 g/mL at 25 °C(lit.)
vapor density 2.6 (vs air)
vapor pressure 12.5 mm Hg ( 20 °C)
refractive index n20/D 1.397(lit.)
Flash point 80 °F
storage temp. Store at +5°C to +30°C.
solubility 125g/l
form Liquid
pka >14 (Schwarzenbach et al., 1993)
color Colorless
Relative polarity 0.506
Odor Strong, pleasant.
PH Range 7
Odor Type fruity
Odor Threshold 0.22ppm
explosive limit 1.4-9.8%(V)
Water Solubility 12.5 g/100 mL (20 ºc)
Sensitive Hygroscopic
Merck 14,1541
BRN 1718765
Henry's Law Constant 1.19 (static headspace-GC, Merk and Riederer, 1997)
Dielectric constant 15.8(25℃)
Exposure limits TLV-TWA 450 mg/m3 (150 ppm) (NIOSH), 305 mg/m3 (100 ppm) (ACGIH); IDLH 10,000 ppm.
Stability Stable. Flammable. Substances to be avoided include acids, acid chlorides, acid anhydrides, oxidizing agents and halogens.
InChIKey BTANRVKWQNVYAZ-UHFFFAOYSA-N
LogP 0.610
CAS DataBase Reference 78-92-2(CAS DataBase Reference)
NIST Chemistry Reference 2-Butanol(78-92-2)
EPA Substance Registry System 2-Butanol (78-92-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07
Signal word  Warning
Hazard statements  H226-H319-H335-H336
Precautionary statements  P210-P233-P240-P241-P242-P305+P351+P338
Hazard Codes  Xi
Risk Statements  10-36/37-67
Safety Statements  13-24/25-26-46-7/9
OEB A
OEL TWA: 100 ppm (305 mg/m3), STEL: 150 ppm (455 mg/m3)
RIDADR  UN 1120 3/PG 3
WGK Germany  1
RTECS  EO1750000
Autoignition Temperature 761 °F
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29051490
Toxicity LD50 orally in Rabbit: 6480 mg/kg LD50 dermal Rat > 2000 mg/kg
IDLA 2,000 ppm
NFPA 704
3
1 0

2-Butanol price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) B85919 2-Butanol ReagentPlus?, ≥99% 78-92-2 1L ₹2998.53 2022-06-14 Buy
Sigma-Aldrich(India) B85919 2-Butanol ReagentPlus?, ≥99% 78-92-2 2.5L ₹5932.1 2022-06-14 Buy
Sigma-Aldrich(India) PHR1563 2-Butanol Pharmaceutical Secondary Standard; Certified Reference Material 78-92-2 3X1.2ML ₹9233.73 2022-06-14 Buy
Sigma-Aldrich(India) B85919 2-Butanol ReagentPlus?, ≥99% 78-92-2 20L ₹26391.35 2022-06-14 Buy
Sigma-Aldrich(India) 96870 2-Butanol analytical standard 78-92-2 1ML ₹4860.43 2022-06-14 Buy
Product number Packaging Price Buy
B85919 1L ₹2998.53 Buy
B85919 2.5L ₹5932.1 Buy
PHR1563 3X1.2ML ₹9233.73 Buy
B85919 20L ₹26391.35 Buy
96870 1ML ₹4860.43 Buy

2-Butanol Chemical Properties,Uses,Production

Chemical Properties

Colourless liquid

Physical properties

Clear, colorless, flammable liquid with a pleasant odor. Experimentally determined detection and recognition odor threshold concentrations were 400 μg/m3 (120 ppbv) and 1.2 mg/m3 (410 ppbv), respectively (Hellman and Small, 1974).

Uses

2-Butanol is used in the production of methylethyl ketone and sec-butyl acetate, as asolvent in lacquers and alkyd enamels, inhydraulic brake fluids, in cleaning compounds,and its xanthate derivatives in oreflotation.

Production Methods

2-Butanol is produced commercially by the indirect hydration of n-butenes.

Definition

ChEBI: A secondary alcohol that is butane substituted by a hydroxy group at position 2.

General Description

A clear colorless liquid with an alcohol odor. Flash point below 0 °F. Less dense than water. Vapors heavier than air. Soluble in water. Moderately irritates the eyes and skin. Prolonged and repeated contact may cause defatting and drying of the skin. Vapors may irritate the nose, throat and respiratory tract. May be harmful by ingestion.

Air & Water Reactions

Highly flammable. Soluble in water.

Reactivity Profile

Attacks plastics. [Handling Chemicals Safely 1980. p. 236]. Acetyl bromide reacts violently with alcohols or water (Merck 11th ed. 1989). Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid [Chem. Eng. News 45(43):73 1967; J, Org. Chem. 28:1893 1963]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites [NFPA 491 M 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence [Wischmeyer 1969].

Hazard

Toxic, mutagenic, upper respiratory tract irritant, central nervous system impairment.

Health Hazard

Exposure to 2-butanol may cause irritationof the eyes and skin. The latter effect isproduced by its defatting action on skin. Thistoxic property is mild and similar to thatof other butanol isomers. High concentrationmay produce narcosis. The narcotic effect isstronger than that of n-butanol, probably dueto the higher vapor pressure of the secondaryalcohol.
The toxicity is lower than that of itsprimary alcohol analogue.
LD50 value, oral (rats): 6480 mg/kg.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Poison by intravenous and intraperitoneal routes. Mildly toxic by ingestion. Experimental reproductive effects. A skin and eye irritant. See also nBUTYL ALCOHOL and ALCOHOLS. Dangerous fire hazard when exposed to heat or flame. Auto-oxidizes to an explosive peroxide. Ignites on contact with chromium trioxide. To fight fire, use water spray, alcohol foam, CO2, dry chemical. Incompatible with oxidizing materials. When heated to decomposition it emits acrid smoke and fumes.

Potential Exposure

Butyl alcohols are used as solvents for paints, lacquers, varnishes, natural and synthetic resins, gums, vegetable oils, dyes, camphor, and alkaloids. They are also used as an intermediate in the manufacture of pharmaceuticals and chemicals; in the manufacture of artificial leather, safety glass; rubber and plastic cements, shellac, raincoats, photographic films, perfumes; and in plastic fabrication.

Environmental Fate

Biological. Bridié et al. (1979) reported BOD and COD values of 2.15 and 2.49 g/g using filtered effluent from a biological sanitary waste treatment plant. These values were determined using a standard dilution method at 20 °C for a period of 5 d. The ThOD for sec-butyl alcohol is 2.59 g/g. In activated sludge inoculum, following a 20-d adaptation period, 98.5% COD removal was achieved. The average rate of biodegradation was 55.0 mg COD/g?h (Pitter, 1976).
Photolytic. The estimated half-life of sec-butyl alcohol for the reaction of OH radicals in air ranges from 129 d to 23 yr (Anbar and Neta, 1967).
Chemical/Physical. sec-Butyl alcohol will not hydrolyze in water because it does not contain a hydrolyzable group (Kollig, 1993).

Shipping

UN1120 Butanols, Hazard Class: 3; Labels: 3— Flammable liquid. UN1212 Isobutanol or Isobutyl alcohol, Hazard Class: 3; Labels: 3—Flammable liquid

Purification Methods

Purification methods are the same as for n-Butanol. These include drying with K2CO3 or CaSO4, followed by filtration and fractional distillation, refluxing with CaO, distillation, then refluxing with magnesium and redistillation, and refluxing with, then distilling from CaH2. Calcium carbide has also been used as a drying agent. The anhydrous alcohol is obtained by refluxing with sec-butyl phthalate or succinate. (For method see Ethanol.) Small amounts of alcohol can be purified via conversion to the alkyl hydrogen phthalate and recrystallisation [Hargreaves J Chem Soc 3679 1956]. For purification of optical isomers, see Timmermans and Martin [J Chem Phys 25 411 1928]. [Beilstein 2 III 1566.]

Incompatibilities

Butyl alcohols may form explosive mixture with air. In all cases they are 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. Attacks some plastics, rubber and coatings. n-Butanol is incompatible with strong acids; halogens, caustics, alkali metals; aliphatic amines; isocyanates. sec-Butanol forms an explosive peroxide in air. Ignites with chromium trioxide. Incompatible with strong oxidizers; strong acids; aliphatic amines; isocyanates, organic peroxides. tert-Butanol is incompatible with strong acids (including mineral acid), including mineral acids; strong oxidizers or caustics, aliphatic amines; isocyanates, alkali metals (i.e., lithium, sodium, potassium, rubidium, cesium, francium). isoButanol is incompatible with strong acids; strong oxidizers; caustics, aliphatic amines; isocyanates, alkali metals and alkali earth. May react with aluminum at high temperatur

Waste Disposal

Incineration, or bury absorbed waste in an approved land fill.

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