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US4510306A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for purifying reaction products containing higher-alkyl glycosides

Assignee: BASF Corp
•
Filing: 1983-09-13
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Granted: 1985-04-09
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Expires: 2003-09-13
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Abstract

Abstract The subject invention relates to the removal of residual higher alcohols which are present from the preparation of crude higher-alkyl glycosides. The residual higher alcohols are removed via vacuum distillation with a hydroxyl-containing solvent. The purified higher-alkyl glycosides are biodegradable nonionic surfactants which are soluble and stable in highly alkaline cleaning formulations used for bottle washing, metal cleaning, textile treatment and other applications.

Inventors

  • 👤 William K. Langdon

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 10:18
CPC Classifications
C; C07; C07H; C07H15/00; C07H15/02; C07H15/04

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 147 words
A process for purifying crude higher-alkyl glycosides containing residual free higher alcohols, said glycosides obtained by the acid catalyzed reaction of C 8 -C 18 aliphatic monohydric alcohols with a source of monosaccharide, which comprises partially distilling a mixture of the crude higher-alkyl glycoside and a hydroxyl containing solvent selected from the group consisting of: (a) glycerol, (b) polyoxyalkylene glycols having an average of 3 to about 5 oxyalkylene units selected from oxyethylene and oxypropylene, (c) C 1 -C 4 alkyl ethers of polyoxyalkylene glycols having about 2 to about 5 oxyalkylene units selected from oxyethylene and oxypropylene, and (d) C 1 -C 4 alkyl ethers of aliphatic diols, triols, and tetrols having no more than 4 carbon atoms, wherein further, the boiling point of the solvent is at least 10° C. higher than that of the higher alcohol used in the preparation of the higher-alkyl glycoside.
Claim 2
Dependent Claim 147 words
A process for purifying crude higher-alkyl glycosides containing residual free higher alcohols, said glycosides obtained by the acid catalyzed reaction of C 8 -C 18 aliphatic monohydric alcohols with a source of monosaccharide, which comprises partially distilling a mixture of the crude higher-alkyl glycoside and a hydroxyl containing solvent selected from the group consisting of: (a) glycerol, (b) polyoxyalkylene glycols having an average of 3 to about 5 oxyalkylene units selected from oxyethylene and oxypropylene, (c) C 1 -C 4 alkyl ethers of polyoxyalkylene glycols having about 2 to about 5 oxyalkylene units selected from oxyethylene and oxypropylene, and (d) C 1 -C 4 alkyl ethers of aliphatic diols, triols, and tetrols having no more than 4 carbon atoms, wherein further, the boiling point of the solvent is at least 10° C. higher than that of the higher alcohol used in the preparation of the higher-alkyl glycoside.
Claim 3
Dependent Claim 31 words
The process of claim 1 wherein the amount of the hydroxyl-containing solvent used is from 5 percent to about 20 percent by weight based upon the weight of the higher-alkyl glycoside.

References Cited (Backward Citations)

US2559519A Cited
US3580850A Cited
US3598865A Cited
US3772269A Cited
DE3001064A1 Cited
US4349669A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-04-08 1988-10-08 1989-04-09 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-04-08 1992-10-08 1993-04-09 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-04-08 1996-10-08 1997-04-09 $7700.00 Window Closed / Lapsed

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