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Amadis Chemical offer CAS#106-88-7;CAT#A801527
Cas No: 106-88-7
No Data 10 Milligram Amadis Chemical Co., Ltd. Contact Supplier
1,2-Butylene oxide
Cas No: 106-88-7
No Data No Data No Data Chemwill Asia Co., Ltd. Contact Supplier
1,2-Epoxybutane
Cas No: 106-88-7
No Data 1 Kilogram 1-100 Metric Ton/Month Hangzhou Dayangchem Co., Ltd. Contact Supplier
1,2-epoxybutane
Cas No: 106-88-7
No Data 5 Metric Ton 800 Metric Ton/Month Henan Sinotech Import&Export Corporation Contact Supplier
106-88-7 C4H8O 1,2-EPOXYBUTANE
Cas No: 106-88-7
No Data 100 Gram 1 Kilogram/Day HENAN SUNLAKE ENTERPRISE CORPORATION Contact Supplier
TIANFUCHEM-- 106-88-7--1,2-EPOXYBUTANE in stock
Cas No: 106-88-7
USD $ 2000.0-2000.0 / Metric Ton 1 Metric Ton 1000 Metric Ton/Day Henan Tianfu Chemical Co., Ltd. Contact Supplier
Hot sale 1,2-EPOXYBUTANE cas 106-88-7
Cas No: 106-88-7
No Data 1 Kilogram 1000 Metric Ton/Week Crovell Biotech (Hebei) Co., Ltd. Contact Supplier
Hot sale 1,2-EPOXYBUTANE cas 106-88-7
Cas No: 106-88-7
No Data 5 Gram 1000 Metric Ton/Day Weifang Tansen Yiang international trading co., LTD Contact Supplier
Nice Quality 1,2-Butylene oxide Cas No: 106-88-7
Cas No: 106-88-7
USD $ 1.0-3.0 / Gram 10 Gram 1000 Kilogram/Month Wuhan Monad Medicine Tech Co.,LTD Contact Supplier
1,2-Epoxybutane CAS NO.106-88-7
Cas No: 106-88-7
No Data 10 Gram 100 Kilogram/Week Jilin Tely Imp.& Exp.Co., Ltd. Contact Supplier

106-88-7 Usage

Air & Water Reactions

Highly flammable. Soluble in water and may decompose upon contact with water.

Fire Hazard

Behavior in Fire: Containers may explode in fire. Use water to cool container from safe distance.

Reactivity Profile

Epoxides, such as 1,2-EPOXYBUTANE, are highly reactive. They polymerize in the presence of catalysts or when heated. Contact with anhydrous metal halides; amino, hydroxyl and carboxyl functions; inorganic acids and charcoal may cause polymerization. These polymerization reactions can be violent. Compounds in this group react with acids, bases, and oxidizing and reducing agents. They react, possibly violently with water in the presence of acid and other catalysts.

Chemical Properties

colourless liquid with an unpleasant smell

General Description

A clear colorless volatile liquid with an ethereal odor. Flash point near 0°F. Density about 6.9 lb / gal. Soluble in water. Boiling point near 140°F. Flammable over a wide range of vapor-air concentrations. May polymerize with the evolution of heat and possible rupture of container if contaminated. Vapors irritate eyes, skin and respiratory system. Prolonged contact with skin may cause in delayed burns. Vapors are heavier than air. Used as an intermediate to make various polymers. Chemicals that polymerize are often stabilized by refrigeration.

Health Hazard

Inhalation: intolerable odor and irritation; respiratory injury may occur at higher levels. Ingestion causes irritation of mouth and stomach. Contact with either liquid or vapor may cause burns of eyes. Liquid produces frostbite-type of skin burn if free to evaporate; if confined to skin, burn may cause skin sensitization; not readily absorbed in toxic amounts.

Purification Methods

Dry it with CaSO4, and fractionally distil it through a long (126cm) glass helices-packed column. The first fraction contains a water azeotrope. [Beilstein 17 II 17.]
InChI:InChI=1/C4H8O/c1-2-4-3-5-4/h4H,2-3H2,1H3/t4-/m1/s1

106-88-7 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Aldrich (109975)  1,2-Epoxybutane  99% 106-88-7 109975-1L 916.11CNY Detail
Aldrich (109975)  1,2-Epoxybutane  99% 106-88-7 109975-250ML 596.70CNY Detail

106-88-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Epoxybutane

1.2 Other means of identification

Product number -
Other names Ethylethylene Oxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. The primary use of 1,2-epoxybutane is as a stabilizer in chlorinated hydrocarbon solvents. 1,2-Epoxybutane is used in the production of the corresponding butylene glycols and their derivatives. It is also used to make butanolamines, surface-active agents, and gasoline additives.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:106-88-7 SDS

106-88-7Downstream Products

106-88-7Related news

Polymer paperPhotopolymerization of 1,2-epoxypropane and 1,2-EPOXYBUTANE (cas 106-88-7) by arenediazonium salts: evidence for anion dependence of the extent of polymerization08/26/2019

The rates and extents of polymerization of 1,2-epoxypropane and 1,2-epoxybutane, induced by photolysis of dilute concentrations of salts of 2,5-diethoxy-4-tolylthiobenzenediazonium ion with various Lewis acids (SbF−6, PF−6, BF−4 etc.) have been determined by viscosity, 1H n.m.r. and polymer isol...detailed

Excess molar enthalpies of eight binary mixtures containing 1,2-EPOXYBUTANE (cas 106-88-7) + ethyl alkanoates at 298.15 K08/22/2019

Excess molar enthalpies, HEm, have been measured using a flow microcalorimeter at 298.15 K and at atmospheric pressure for the eight mixtures containing 1,2-epoxybutane with ethyl acetate, ethyl propanoate, ethyl butyrate, ethyl pentanoate, ethyl hexanoate, ethyl heptanoate, ethyl octanoate and ...detailed

Isomerization and hydrogenolysis of 1,2-EPOXYBUTANE (cas 106-88-7) on platinum08/20/2019

The transformation of 1,2-epoxybutane on PtCandPtCr2O3 catalysts in the presence of hydrogen has been studied in a flow apparatus at atmospheric pressure and in the temperature range 160–190 °C. Parallel formation of butanal, 2-butanone, 1-butanol, and 2-butanol has been observed. The selectiv...detailed

PaperStereospecific formation of 1,2-epoxypropane, 1,2-EPOXYBUTANE (cas 106-88-7) and 1-chloro-2,3-epoxypropane by alkene-utilizing bacteria08/18/2019

Resting cells of ethene grown Mycobacterium 2W produced 1,2-epoxypropane stereospecifically from propene as revealed by optical rotation, 1H n.m.r. using a chiral shift reagent, and also by complexation gas chromatography involving a glass capillary column coated with an optically active metal c...detailed

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