7 HOOKER ACID CHLORIDES You should know... - C&EN Global

Nov 5, 2010 - Advertisements that appeared within the print issues of Chem. Eng. News have been included in the C&EN Archives to provide a ...
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HOOKER ACID CHLORIDES

You should

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As a major producer of high quality chlorine, Hooker is able to manu­ facture acid chlorides of high purity a n d uniformity. If you are working with dyestuffs, plasticizers, pharmaceuticals, lubricants or in other proc­ essing fields where you r e q u i r e good quality acid chlorides, you should check into these H o o k e r products. T h e acid chlorides Hooker can supply are listed below with brief information about their physical and chemical characteristics and their uses. More complete information is given on individual Technical Data Sheets available when requested on your business letterhead. Hooker's Technical Staff is also ready to work with you on the application of Hooker chemicals to your specific problems. PRODUCT

DESCRIPTION AND USES

PRODUCT

DESCRIPTION AND USES

Chemical Formula and Molecular Weight

Chemical Formula and Molecular Weight

Metanitrobenzoyl Chloride N02C6H4COCI;185.5

Yellow to brown liquid partially crystallized at room temperature. Last crystal point 28° to 31 ° C . Manufacture of dyes for fabrics and color photography; intermediate in preparation of pharmaceuticals.

Phosgene (Carbonyl Chloride) COCI 2 ;98.9

Liquified gas. F.P. —126°C, B . I \ 8.2°C. Manufacture alkyl and aryl chlorocarbonates and dialkylcarbonates; dye intermediates; metal chlor­ ides and anhydrides; pharmaceu­ ticals; perfumes.

Paranitrobenzoyl Chloride

Yellow crystalline solid. M.P. 70° C minimum. Manufacture of novo-

Sulfuryl Chloride SO 2 CI 2 ;135.0

Light yellow liquid. B.R. 2° incl. 69.5°C. Reacts with organic acids to form other chlorides and anhydrides. Chlorinating agent for chlorophenol and other chlorination reactions in organic synthesis.

Thionyl Chloride SOCI 2 ;119.0

Clear, pale yellow to red liquid. Re­ fined Grade, 97.5% min. SOCl 2 ; Technical Grade, 93-f-%. Manufac­ ture of organic acid chlorides and anhydrides, alky] chlorides from cor­ responding alcohols. It may be used to introduce sulfur alone or in com­ bination with oxygen.

N0 2 C 6 H 4 COCI;185.5 ™ £ Acetyl Chloride CH 3 COCI;78.5

Benzoyl Chloride C 6 H 5 COCI;140.5

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Clear, colorless to pale yellow liquid. Dist. R. 2.5° incl. 51 ° C. T o introduce acetyl group into organic compounds. Manufacture of intermediates, dyes, and pharmaceuticals. Clear, colorless liquid. Boiling point 198° C. As a highly reactive acid chloride, it may be used to introduce the benzoyl group into organic com­ pounds, especially through FriedelCrafts reactions. It is used in the manufacture of synthetic perfumes, pharmaceuticals, dyes and resins.

7 FORTY-SEVENTH ST., NIAGARA FALLS, Ν. Υ. NEW YORK, N. Y.

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WILMINGTON, CALIF.

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TACOMA, WASH.

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SODIUM SULFIDE . SODIUM SULFHYDRATE · SODIUM TETRASULFIDE · CAUSTIC SODA · MURIATIC ACID · PARADICHLOROBENZENE · CHLORINE

VOLUME

2 7,

NO.

32

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1949

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