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Isobutyl isocyanate

CAS No.
1873-29-6
Chemical Name:
Isobutyl isocyanate
Synonyms
Isobutyl isocyanate;2-methylpropyl isocyanate;Isobutyl isocyanate USP/EP/BP;isocyanic acid isobutyl ester;Propane, 1-isocyanato-2-methyl-
CBNumber:
CB0852506
Molecular Formula:
C5H9NO
Molecular Weight:
99.13
MDL Number:
MFCD00036022
MOL File:
1873-29-6.mol
MSDS File:
SDS
Last updated:2023-05-04 15:16:09

Isobutyl isocyanate Properties

Melting point 85.5°C (estimate)
Boiling point 125.62°C (estimate)
Density 0.9570 (estimate)
refractive index 1.4061 (estimate)
CAS DataBase Reference 1873-29-6
FDA UNII 69A68W7YAE
EPA Substance Registry System Propane, 1-isocyanato-2-methyl- (1873-29-6)

Isobutyl isocyanate price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC I784900 IsobutylIsocyanate 1873-29-6 2.5g $145 2021-12-16 Buy
Oakwood 044447 1-Isocyanato-2-methylpropane 98% 1873-29-6 5g $190 2021-12-16 Buy
Medical Isotopes, Inc. 70956 IsobutylIsocyanate 1873-29-6 1g $610 2021-12-16 Buy
American Custom Chemicals Corporation CHM0080071 1-ISOCYANATO-2-METHYLPROPANE 95.00% 1873-29-6 1G $794.34 2021-12-16 Buy
Medical Isotopes, Inc. 70956 IsobutylIsocyanate 1873-29-6 5G $875 2021-12-16 Buy
Product number Packaging Price Buy
I784900 2.5g $145 Buy
044447 5g $190 Buy
70956 1g $610 Buy
CHM0080071 1G $794.34 Buy
70956 5G $875 Buy

Isobutyl isocyanate Chemical Properties,Uses,Production

Uses

Isobutyl Isocyanate, is an building block that cna be used for the synthesis of Boceprevir (B674500), a novel, potent, selective, orally bioavailable NS3 protease inhibitor used for the treatment of Hepatitis C virus (HCV) infection.

General Description

A colorless liquid. Flash point near 40°F. Less dense than water. Contact may severely irritate skin, eyes and mucous membranes. May be very toxic by ingestion, inhalation and skin absorption. Used to make pesticides and pharmaceuticals.

Air & Water Reactions

Highly flammable. Soluble in water.

Reactivity Profile

Isocyanates and thioisocyanates, such as Isobutyl isocyanate, are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. 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)].

Health Hazard

TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Bromoacetates and chloroacetates are extremely irritating/lachrymators. 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

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors 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. Substance will react with water (some violently) releasing flammable, toxic or corrosive gases and runoff. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water.

Isobutyl isocyanate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 14)Suppliers
Supplier Tel Email Country ProdList Advantage
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Propane, 1-isocyanato-2-methyl- Isobutyl isocyanate 2-methylpropyl isocyanate isocyanic acid isobutyl ester Isobutyl isocyanate USP/EP/BP 1873-29-6 CH32CHCH2NCO