Acidic heteropolysaccharide AM-2
First Claim
Patent Images
1. Acidic heteropolysaccharide AM-2 having the following physiochemical characteristics:
- (1) compositioncomposed of glucose, rhamnose, mannose, glucuronic acid and acetyl group as main components, the molar ratio of glucose;
rhamnose;
mannose;
glucuronic acid being 4;
0.9˜
1.1;
0.9˜
1.1;
0.9˜
1.1 and the acetyl group content is 4 to 8%;
(2) infrared spectrumthe infrared spectrum is as shown in FIG. 1;
(3) color reactionAnthrone reaction;
positiveCarbazole reaction;
positiveElson-Morgan'"'"'s reaction;
negativeIodine reaction;
positive;
(4) solubility in solventssoluble in water, and insoluble in ethanol, ether, acetone;
(5) color and appearancethe purified polysaccharide is white, cottony or fibrous;
(6) viscositythe aqueous solution is colorless, transparent and viscous, and the viscosity of 1% solution is 1200 to 2000 cps as determined with a torque measuring viscometer at 25°
C. and a rate of 30 rpm;
(7) elemental analysis;
C;
39.9±
1%;
H;
6.2±
1%;
N;
0%;
ash;
3.0±
1.0%;
(8) Specific rotation[α
]D27 =0˜
+20(C=0.33 in the aqueous solution);
(9) molecular weightabout 105 or above;
(10) melting pointthe polysaccharide turns dark brown at 190°
C. and decomposes at 250°
C.; and
(11) nuclear magnetic resonance spectrumthe 13 C-nuclear magnetic resonance spectrum is as shown in FIG. 7.
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Abstract
Novel highly viscous acidic heterpolysaccharide AM-2 is produced from a strain of genus Acetobacter isolated from vinegar mash, and is useful as an adhesive, coating agent, drilling mud additive, enhanced oil recovering agent, etc., as well as a material useful for the production of foods, drugs and cosmetics because of its safety and high viscosity.
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1 Claim
-
1. Acidic heteropolysaccharide AM-2 having the following physiochemical characteristics:
-
(1) composition composed of glucose, rhamnose, mannose, glucuronic acid and acetyl group as main components, the molar ratio of glucose;
rhamnose;
mannose;
glucuronic acid being 4;
0.9˜
1.1;
0.9˜
1.1;
0.9˜
1.1 and the acetyl group content is 4 to 8%;(2) infrared spectrum the infrared spectrum is as shown in FIG. 1; (3) color reaction Anthrone reaction;
positiveCarbazole reaction;
positiveElson-Morgan'"'"'s reaction;
negativeIodine reaction;
positive;(4) solubility in solvents soluble in water, and insoluble in ethanol, ether, acetone; (5) color and appearance the purified polysaccharide is white, cottony or fibrous; (6) viscosity the aqueous solution is colorless, transparent and viscous, and the viscosity of 1% solution is 1200 to 2000 cps as determined with a torque measuring viscometer at 25°
C. and a rate of 30 rpm;(7) elemental analysis; C;
39.9±
1%;
H;
6.2±
1%;
N;
0%;
ash;
3.0±
1.0%;(8) Specific rotation [α
]D27 =0˜
+20(C=0.33 in the aqueous solution); (9) molecular weight about 105 or above; (10) melting point the polysaccharide turns dark brown at 190°
C. and decomposes at 250°
C.; and(11) nuclear magnetic resonance spectrum the 13 C-nuclear magnetic resonance spectrum is as shown in FIG. 7.
-
Specification