CONCORD GRAPE SUGAR RIBULOSE

<body topmargin=0 leftmargin=0 marginheight=0 marginwidth=0> <table cellpadding=0 cellspacing=0 border=0><tr> <td valign="top" height=30 BGCOLOR="#006699" TEXT="#080000"> <div> <FONT SIZE="2" COLOR="#FFFBF0" FACE="Arial" ><B>CHEMISTRY SCHOOL</B></FONT><FONT SIZE="1" COLOR="#FFFBF0" FACE="Arial" ><B> </B></FONT><B>  </B><FONT SIZE="1" COLOR="#FFFBF0" FACE="Arial" ><B> </B><A HREF="index.htm" TARGET="_top" TITLE="CHEMISTRY SCHOOL"><U>HOME PAGE</U></A><B>  • </B> <A HREF="sugars_and_carbohydrates.htm" TARGET="_top" TITLE="WHAT ARE SUGARS and CARBOHYDRATES"><U>SUGARS & CARBOHYDRATES • INDEX</U></A>               </FONT>      RIBULOSE <B> •</B> <I>RAI-BIEU-LOHS </I><I><B> </B></I><B>    </B></div> </td> </tr><tr> <td valign="top" height=450 BGCOLOR="#FFFFCC" TEXT="#080000"> <div> <TABLE BORDER="1" CELLPADDING="6" CELLSPACING="0" WIDTH="765" BORDERCOLORLIGHT="#993380" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" BGCOLOR=#FFFFCC > <tR> <tD VALIGN=CENTER BGCOLOR=#FFCCB2 HEIGHT= 86 WIDTH="189"><div> <IMG SRC="17175c510.gif" border=0 width="92" height="81" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </tD> <tD VALIGN=CENTER BGCOLOR=#FFCCB2 WIDTH="546"><div> <B>RIBULOSE</B></div> <div> <B>CONCORD GRAPE SUGAR</B></div> </tD> </tR> <tR> <tD VALIGN=TOP HEIGHT= 384 ><NOBR><div> <IMG SRC="cb9b8b20.gif" border=0 width="184" height="178" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> A HEED FRONTAL STUDY OF </div> <div> CONCORD GRAPE SUGAR</div> <div> RIBULOSE</div> <div> 1982   -159°C </div> <bR> <div>    EACH BLACK DOT, IS A HIT,</div> <div>    BY A POSITRON ELECTRON, </div> <div>    UPON THE NUCLEUS, </div> <div>    OF ONE OF THE ATOMS,</div> <div>    IN THE FROZEN </div> <div>    TRI-SACCHARDIDE</div> </NOBR></tD> <tD VALIGN=TOP BGCOLOR=#FFFFCC><NOBR><div> <TABLE BORDER="0" CELLPADDING="2" CELLSPACING="1" WIDTH="545" BORDERCOLORLIGHT="#C0C0C0" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=TOP HEIGHT= 335 ><NOBR><div> NATURAL RIBULOSE, HAS BEEN STUDIED, </div> <div> BY MANY DOCTORS & AGRO-SCIENTISTS,</div> <div> BUT NO ONE, IN THE USA, HAS EVER BEEN ABLE, </div> <div> TO SYNTHESIZE, RIBULOSE, BECAUSE THEY THOUGHT,</div> <div> THAT IT SHOULD BE,  DERIVED FROM ERYTHRULOSE,</div> <div> AS SCIENTISTS IN THE 1890's, THEORIZED.</div> <div> THE HEED STUDY OF RIBULOSE, ON THE LEFT,</div> <div> CHANGED ALL OF THAT, FALLACIOUS THINKING, FOREVER.</div> <div> AS SOON AS, DR. JONAS SALK, SAW IT, HE SAID TO HIMSELF,</div> <div> SOMEWHERE, I HAVE SEEN THAT STUDY BEFORE.</div> <div> HE ASKED WANDA, HIS ASSISTANT, TO SEARCH THEIR FILES, </div> <div> FOR A STUDYS, EXACTLY EQUAL, TO THE RIBULOSE STUDY. </div> <div> WITHIN MINUTES, SHE BROUGHT FORTH A STUDY,</div> <div> SENT BY THE BIOCHEMIST BEN THOMPSON, SOME TIME AGO,</div> <div> WHICH SHOWED, A TRI-CYCLIC, BI-ETHYL ESTER CARBONATE,</div> <div> THAT HE FOUND ADJACENT, TO D- RIBULOSE MOLECULES,</div> <div> IN HIS STUDYS, OF GREEN GRAPE & WINE GRAPE SUGARS.</div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cbda79f0.gif" border=0 width="167" height="159" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> A HEED SIDE STUDY OF</div> <div> THOMPSON GREEN  GRAPE </div> <div> TRI-CYCLIC</div> <div> BI-ETHYL CARBONATE</div> <div> 1957 <B>-</B>182°C</div> <bR> <bR> <bR> </NOBR></tD> </tR> </TABLE></div> <div>  THAT IS VERY INTERESTING, HE SAID TO WANDA, </div> <div>  LET US ANALYZE, THE TWO OF THEM MORE CLOSELY. </div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 52 WIDTH="737"><div> <B>ANALYZING THE TWO STUDYS</B></div> </tD> </tR> <tR> <tD VALIGN=TOP HEIGHT= 395 ><NOBR><div> <IMG SRC="cb7a79e0.gif" border=0 width="167" height="158" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"><FONT SIZE="1" COLOR="#000000" FACE="Arial" >  </FONT></div> <div>  CIRCLES DRAWN AROUND</div> <div>  THE NUCLEAR HITS </div> <div> REVEAL THE MOLECULAR FORM</div> <div> OF TRI-CYCLIC</div> <div> BI-ETHYL ESTER CARBONATE</div> </NOBR></tD> <tD VALIGN=TOP BGCOLOR=#FFFFCC><NOBR><div> <TABLE BORDER="0" CELLPADDING="1" CELLSPACING="1" WIDTH="545" BORDERCOLORLIGHT="#C0C0C0" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=CENTER HEIGHT= 308 ><NOBR><div> THEY ANALYZED THE CARBONATE FIRST,</div> <div> BY DRAWING, THE YELLOW CIRCLES, AROUND </div> <div> THE NUCLEAR HITS, IN THE HEED STUDY. </div> <div> AND WITHIN A FEW HOURS, THEY COULD SEE, </div> <div> THAT THE CARBONATE HAD,</div> <div> THREE KETO ETHYL ESTER SIDE BRANCHES, </div> <div> AND A THREE CARBONYL CARBON, </div> <div> THREE EPOCSI OCSION ATOM,</div> <div>  ARENE ALDEHYDIC,CENTRAL CORE.</div> <div> THEN THEY ANALYZED, THE RIBULOSE STUDY,</div> <div> & NOTICED, THAT IT SEEMED TO HAVE, HYDROCSYLS,</div> <div> ON THE END, OF EACH, OF THE KETO ETHYL ESTERS, </div> <div> BUT OTHERWISE, IT WAS  EXACTLY THE SAME.</div> <div> SALK, SAID TO WANDA, TRI-CYCLIC D-RIBULOSE, </div> <div> MAY BE DERIVED, FROM BI-ETHYL ESTER CARBONATE,</div> <div> AND NOT ERYTHRULOSE, AS WE HAVE BEEN TAUGHT.</div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cb5cbb80.gif" border=0 width="203" height="184" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div>  CIRCLES DRAWN AROUND</div> <div>  THE NUCLEAR HITS </div> <div> REVEAL THE MOLECULAR FORM</div> <div> OF TRI-CYCLIC RIBULOSE </div> <div> FROM CONCORD GRAPES</div> </NOBR></tD> </tR> </TABLE></div> <div> SEE, IF YOU CAN FIND SOMEONE, WITH SIDE STUDYS, OF EACH OF THEM. </div> <div> TWELVE WEEKS LATER, THEY RECEIVED A SIDE STUDY, OF BI-ETHYL ESTER CARBONATE, </div> <div>  FROM JEAN LEPROUVE, THE DIRECTOR, OF THE SORBONNE UNIVERSITY, IN FRANCE.</div> <div>  AND SHORTLY AFTER THAT, THEY RECEIVED A SIDE STUDY, OF D-RIBULOSE FROM IUPAC </div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 53 WIDTH="737"><div> <B>COMPARING THE SIDE STUDYS OF THE TWO CHEMICALS</B></div> </tD> </tR> <tR> <tD VALIGN=TOP COLSPAN=2 HEIGHT= 355 ><NOBR><div> <TABLE BORDER="0" CELLPADDING="2" CELLSPACING="1" WIDTH="743" BORDERCOLORLIGHT="#C0C0C0" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=TOP HEIGHT= 254 ><NOBR><div> <IMG SRC="cbf939e0.gif" border=0 width="147" height="158" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> THE STUDY FROM FRANCE</div> <div> OF THE SIDE OF TRI-CYCLIC</div> <div> THE BI-ETHYL ESTER</div> <div> CARBONATE</div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cc1929e0.gif" border=0 width="146" height="158" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> THE CIRCLE STUDY </div> <div> SHOWED THE PAIRED </div> <div> KETO ETHYL ESTER</div> <div> SIDE BRANCHES</div> </NOBR></tD> <tD VALIGN=TOP WIDTH="34"><IMG BORDER="0" SRC="1x1.gif" HEIGHT="254" ALIGN="bottom" WIDTH="34" HSPACE="0" VSPACE="0"></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cbb95b20.gif" border=0 width="149" height="178" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> THE STUDY FROM IUPAC</div> <div> OF THE SIDE OF TRI-CYCLIC</div> <div>  GRAPE D-RIBULOSE</div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cb496b10.gif" border=0 width="150" height="177" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> THE CIRCLE STUDY </div> <div> SHOWED PAIRED </div> <div> HYDROCSI-ETHYL ESTERS</div> </NOBR></tD> </tR> </TABLE></div> <DIV ALIGN="LEFT"></DIV> <div> SALK & WANDA, WORKED 12 WEEKS, ON THESE TWO STUDYS,</div> <div> TO VALIDATE, THEIR CONCLUSIONS, THAT RIBULOSE, IS DERIVED,</div> <div> FROM THE BI-KETO ETHYL ESTER CARBONATE, THAT IS FOUND,</div> <div> WITH TRI-CYCLIC RIBULOSE, IN MANY TYPES OF GRAPES, </div> <div> AND IS ALSO FOUND, WITH RIBULOSE IN OUR SPINES </div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 45 WIDTH="737"><div> <B>COMPARING THE COMPUTER SIMULATIONS</B></div> </tD> </tR> <tR> <tD VALIGN=TOP COLSPAN=2 HEIGHT= 329 ><NOBR><div> <TABLE BORDER="1" CELLPADDING="1" CELLSPACING="0" WIDTH="749" BORDERCOLORLIGHT="#FFCCB2" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=CENTER COLSPAN=2 HEIGHT= 19 WIDTH="383"><div> VIEWS FROM THE FRONT</div> </tD> <tD VALIGN=CENTER COLSPAN=2 WIDTH="352"><div> VIEWS FROM THE SIDE</div> </tD> </tR> <tR> <tD VALIGN=TOP HEIGHT= 161 ><NOBR><div> <IMG SRC="cc4a58e0.gif" border=0 width="165" height="142" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cc7a79c0.gif" border=0 width="167" height="156" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cc682920.gif" border=0 width="130" height="146" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cc27a990.gif" border=0 width="122" height="153" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER HEIGHT= 42 WIDTH="193"><div> KETO-ETHYL ESTER </div> <div> CARBONATE</div> </tD> <tD VALIGN=CENTER><NOBR><div> KETO HYDROCSI ETHYL </div> <div> ESTER D-RIBULOSE</div> </NOBR></tD> <tD VALIGN=CENTER WIDTH="180"><div> KETO-ETHYL ESTER </div> <div> CARBONATE</div> </tD> <tD VALIGN=CENTER><NOBR><div> KETO HYDROCSI ETHYL </div> <div> ESTER D-RIBULOSE</div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 HEIGHT= 69 ><NOBR><div>   THE ADDITION OF ONLY SIX HYDROCSYLS, TO THE CARBONATE,</div> <div>   TRANSFORMS IT, INTO A TRI-CYCLIC RIBULOSE MOLECULE,</div> <div>   THESE CARBONATES ARE IN BEANS, FILBERTS & COOKED PEAS</div> </NOBR></tD> <tD VALIGN=CENTER COLSPAN=2><NOBR><div>     ALONE, THIS CARBONATE, IS FOUND IN BARK & ROOTS,</div> <div>     COMBINED WITH, TRI-CYCLIC RIBULOSE OR FRUCTOSE,</div> <div>     IT CAN MAKE PROTEIN STRANDS, AS WE SEE BELOW.</div> </NOBR></tD> </tR> </TABLE></div> <DIV ALIGN="LEFT"></DIV> <div>  CARBON ATOMS ARE RED, OCSION ATOMS ARE SKY BLUE, HYDRON ATOMS ARE YELLOW-GOLD</div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 50 WIDTH="737"><div> <B>HOW WE MAKE OUR PROTEIN</B></div> </tD> </tR> <tR> <tD VALIGN=TOP COLSPAN=2 HEIGHT= 960 ><NOBR><div> <TABLE BORDER="1" CELLPADDING="2" CELLSPACING="0" WIDTH="748" BORDERCOLORLIGHT="#FFCCB2" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=TOP HEIGHT= 200 ><NOBR><div> <IMG SRC="cc9b2c20.gif" border=0 width="178" height="194" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="ccbccc30.gif" border=0 width="460" height="195" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER HEIGHT= 78 ><NOBR><div> THE ETHYL ESTER CARBONATES</div> <div> ARE FOUND DIRECTLY IN FRONT & BEHIND</div> <div> TRI-CYCLIC RIBULOSE MOLECULES</div> <div>  IN OUR BACK MUSCLES</div> </NOBR></tD> <tD VALIGN=CENTER><NOBR><div> HERE YOU CAN SEE, EXACTLY HOW THE TWO TYPES, OF TRI-CYCLIC</div> <div> TRIGONAL MOLECULES, LOCATE THEMSELVES, IN MUSCLE TISSUE.</div> <div> BELOW, IS THE IUPAC, LEED STUDY, OF CHICKEN PROTEIN,</div> <div> THAT THESE COMPUTER SIMULATIONS, WERE MADE FROM.</div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER HEIGHT= 320 ><NOBR><div>  IUPAC, HAD ONLY WORKED, WITH FROZEN </div> <div>  CRYSTALS, OF INORGANIC CHEMICALS,</div> <div>  BEFORE THE WORK OF DR.JONAS SALK.</div> <div>  HE WENT TO ENGLAND,TO ASSIST IUPAC </div> <div>  IN THE STUDY OF PROTEIN, BEGUN BY</div> <div>  WARBURG & ROSENBAUM IN THE 1920's</div> <div>  & COMPLETED BY PAULING & ROSENBAUM</div> <div>  IN THE 1940's, THAT WERE DESTROYED BY</div> <div>  ANTI-SEMETIC IUPAC AIDES, IN THE 1990's.</div> <div>  THESE STUDYS LED TO THE DEVELOPMENT</div> <div>  OF SEVERAL, AIDES CURE MEDICINES,</div> <div>  NOW SOLD IN CANADA & SCOTLAND.</div> <div> THE AIDES CURES ARE NOT SOLD,</div> <div> IN THE USA, BECAUSE OF ANTI-SEMETIC,</div> <div> IUPAC & US FDA POLICYS. </div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="ccdccc40.gif" border=0 width="460" height="196" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> A STUDY OF CHICKEN VEIN PROTEIN BY LEIGH & SALK</div> <div> MADE AT THE IUPAC CENTER IN ENGLAND, SHORTLY BEFORE</div> <div> THE IUPAC PUBLIC INFORMATION CENTER WAS MOVED TO THE USA</div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER HEIGHT= 15 WIDTH="263"><IMG BORDER="0" SRC="1x1.gif" HEIGHT="15" ALIGN="bottom" WIDTH="263" HSPACE="0" VSPACE="0"></tD> <tD VALIGN=CENTER WIDTH="471"><IMG BORDER="0" SRC="1x1.gif" HEIGHT="15" ALIGN="bottom" WIDTH="471" HSPACE="0" VSPACE="0"></tD> </tR> <tR> <tD VALIGN=CENTER HEIGHT= 305 ><NOBR><div> <IMG SRC="c7bad890.gif" border=0 width="173" height="137" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> A MICROGRAF OF A LINEAR</div> <div> FIELD OF FROZEN RIBULOSE CRYSTALS</div> <div> MADE IN 1953         -196°C</div> <div> BY KARRER & BREOFFEN</div> <bR> <bR> </NOBR></tD> <tD VALIGN=CENTER><NOBR><div>    IN NATURE, MOLECULES ARE ALWAYS CO-MINGLED WITH OTHER MOLECULES,</div> <div>    TO CREATE, THE MANY QUALITYS, THAT ARE NEEDED, IN EACH TYPE OF CELL,</div> <div>    OR INTERCELLULAR FLUID.</div> <div>    HOWEVER, TO UNDERSTAND, THE STRUCTURE OF A ORGANIC CHEMICAL,</div> <div>    SCIENTISTS VERY OFTEN, SEPARATE THEM & FREEZE THEM, TO STUDY THEM.</div> <div>    WHEN ORGANIC MOLECULES, ARE FROZEN ON GLASS PLATES, </div> <div>    THEY MASS THEMSELVES, IN SPECIFIC FORMS, AND IN DISTINCT PATTERNS, </div> <div>    THAT SCIENTISTS, DESCRIBE IN WORDS, THAT OFTEN, ARE NOT PART, </div> <div>    OF THE VOCABULARY, OF THE AVERAGE PERSON.</div> <div>    WHEN FROZEN, THESE TRI-ANGULAR MOLECULES, OF TRI-CYCLIC RIBULOSE</div> <div>    ARE CALLED BY IUPAC,  PRISMATIC TRIGONAL SHAPED CRYSTALS.</div> <div>    ONE MUST ALWAYS REMEMBER, THAT NO WHERE, IN THE HUMAN BODY,</div> <div>    DO THEY EXIST, AS SHARP GLASS-LIKE CRYSTALS, NOR AS CLOSE PACKED,</div> <div>    AS YOU SEE, IN THIS SUPER FROZEN -198°C, EXTREMELY THIN EXAMPLE.</div> </NOBR></tD> </tR> </TABLE></div> <bR> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 47 WIDTH="737"><div> <B>THE STRUCTURE OF TRI-CYCLIC RIBULOSE</B></div> </tD> </tR> <tR> <tD VALIGN=TOP HEIGHT= 300 ><NOBR><div> <IMG SRC="cf2b8dd0.gif" border=0 width="184" height="221" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> THE STRUCTURAL FORMULA OF </div> <div> RIBUDEN.D-3</div> <div> TRI-CYCLIC D-RIBULOSE </div> </NOBR></tD> <tD VALIGN=TOP BGCOLOR=#FFFFCC><NOBR><div> <TABLE BORDER="0" CELLPADDING="0" CELLSPACING="1" WIDTH="546" BORDERCOLORLIGHT="#C0C0C0" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=TOP HEIGHT= 218 ><NOBR><div> THESE TRIANGULAR, TRI-CYCLIC D-RIBULOSE MOLECULES,</div> <div> WERE CALLED BY THEIR DISCOVERERS, RIBUDEN.D-3 MOLECULES</div> <div> THE `DEN.D-3 ENDING TELLS EVERYONE </div> <div> IT IS A TRI-CYCLIC, DEXTRO-ROTARY, ARENE ALDEHYDE</div> <div> THAT AS A GROUP ARE CALLED TRI-ALDEN SUGARS.</div> <div> THIS NEW ABBREVIATED METHOD OF WRITING ALL,</div> <div> THE QUALIFYING DESCRIPTIONS REQUIRED BY CHEMISTS,</div> <div> IN A SIMPLE 8 LETTER NAME, WITH A 3 LETTER EXTENSION,</div> <div> WILL ALLOW YOU, TO ORGANIZE YOUR FILES ACCURATELY,</div> <div> SO THAT YOU & OTHERS CAN ACCESS THE DATA FOREVER.</div> <div> C:\ BIOCHEM \ SUGARS \ KETONAL \ TRIALDEN.PNT \ RIBUDEN.D-3</div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div> <IMG SRC="cc27a990.gif" border=0 width="122" height="153" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> VIEW OF FROM SIDE OF</div> <div> RIBUDEN.D-3</div> <div> TRI-CYCLIC RIBULOSE</div> </NOBR></tD> </tR> </TABLE></div> <div> IS THE EXACT ADDRESS, FOR YOUR NOTES, ON THIS TRI-ALDEN ALDOSE PENTOSE,</div> <div> YOU CAN COPY THESE SUGAR MOLECULE ILLUSTRATIONS, STRUCTURAL FORMULAS, </div> <div> AND NEW COMPUTER USEABLE FORMULAS, TO WORD PAD OR ANY OTHER PROGRAM</div> <div> FOR YOUR PERSONAL USE.  MULTIPLE COPIES ARE AVAILABLE FROM <A HREF="http://www.chem-data.com" TARGET="_top" TITLE="http://www.chem-data.com"><U>CHEM-DATA.COM</U></A></div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 47 WIDTH="737"><div> <B>THE COMPUTER FORMULA FOR RIBUDEN.....TRI-CYCLIC RIBULOSE</B></div> </tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFFF99 HEIGHT= 138 WIDTH="737"><div> <B>RIBUDEN.D-3 ~ CONCORD GRAPE SUGAR ~ D-RIBULOSE</B></div> <div> A TRI-CYCLIC KETO-PENTOSE ALDEHYDE</div> <div> <B>3(C</B><FONT SIZE="2" COLOR="#660033" FACE="Swiss 721 SWA" ><B>5</B></FONT><B>H</B><FONT SIZE="2" COLOR="#660033" FACE="Swiss 721 SWA" ><B>10</B></FONT><B>O</B><FONT SIZE="2" COLOR="#660033" FACE="Swiss 721 SWA" ><B>5</B></FONT><B>) = 15.CBN+15.OCS+30.HDR </B></div> <div> <B>=</B><FONT SIZE="3" COLOR="#990000" FACE="Swiss 721 SWA" ><B> </B></FONT></div> <div> <B>3 [O+C+2 (O+CH</B><FONT SIZE="1" COLOR="#990000" FACE="Swiss 721 SWA" ><B>2</B></FONT><B>+CH</B><FONT SIZE="1" COLOR="#990000" FACE="Swiss 721 SWA" ><B>2</B></FONT><B>OH ] </B></div> </tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 HEIGHT= 116 ><NOBR><div>    • BIOCHEM / SUGARS / KETONAL / TRIALDEN<B>.</B>PNT / RIBUDEN.D-3 </div> <div>      ARE THE DOS FILE DIRECTORIES,</div> <div>      FOR THIS FORM OF <U>TRI</U>-CYCLIC KETO <U>PENT</U>OSE <U>ALDE</U>HYDE SUGAR</div> <div>    • RIBUDEN<B>.</B>D-3 IS THE WINDOWS FILE NAME FOR THIS FORM</div> <div>      OF DEXTRO-ROTARY, TRI-CYCLIC, RIBULOSE KETO-PENTOSE.</div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 46 WIDTH="737"><div> <B>REDUCED SIZE ILLUSTRATIONS</B></div> </tD> </tR> <tR> <tD VALIGN=TOP COLSPAN=2 HEIGHT= 218 ><NOBR><div> <TABLE BORDER="0" CELLPADDING="2" CELLSPACING="1" WIDTH="620" BORDERCOLORLIGHT="#660033" BORDERCOLORDARK="#660033" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=TOP HEIGHT= 156 WIDTH="97"><IMG BORDER="0" SRC="1x1.gif" HEIGHT="156" ALIGN="bottom" WIDTH="97" HSPACE="0" VSPACE="0"></tD> <tD VALIGN=TOP WIDTH="270"><div> <IMG SRC="c7c937f0.gif" border=0 width="147" height="127" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> FRONT & BACK VIEW</div> </tD> <tD VALIGN=TOP WIDTH="237"><div> <IMG SRC="c7d65800.gif" border=0 width="101" height="128" ALIGN="BOTTOM" HSPACE="0" VSPACE="0"></div> <div> SIDE VIEW</div> </tD> </tR> </TABLE></div> <DIV ALIGN="LEFT"></DIV> <div> CONCORD GRAPE SUGAR, IS A VALUABLE SUGAR, MADE FROM NEAR RIPE CONCORD GRAPES,</div> <div> THAT IS USED, IN ALL OUR MUSCLES, AND ALSO IN OUR LIVER AND PANCREAS.</div> </NOBR></tD> </tR> <tR> <tD VALIGN=CENTER COLSPAN=2 BGCOLOR=#FFCCB2 HEIGHT= 47 ><NOBR><div> <B>               CONCORD GRAPE SUGAR ATTRIBUTES & RECOMMENDATIONS</B></div> </NOBR></tD> </tR> <tR> <tD VALIGN=TOP COLSPAN=2 HEIGHT= 284 ><NOBR><div> <TABLE BORDER="0" CELLPADDING="5" CELLSPACING="1" WIDTH="732" BORDERCOLORLIGHT="#C0C0C0" BORDERCOLORDARK="#808080" FRAME="BOX" RULES="ALL" ALIGN="BOTTOM" HSPACE="0" VSPACE="0" > <tR> <tD VALIGN=TOP HEIGHT= 177 ><NOBR><div>   • RIBUDEN.D-3 ~ RIBULOSE</div> <div>     CONCORD GRAPE SUGAR </div> <div>     IS A TAN TO BEIGE, </div> <div>     VERY SWEET CHEMICAL, </div> <div>     WITH THE TASTE OF BAKED OATS</div> <div>  • IT DOES NOT DISSOLVE EASILY IN COLD WATER </div> <div>  • IT WILL DISSOLVE IN NEAR BOILING WATER</div> <div>  • IT WILL DISSOLVE IN WINES & LIQUEURS.</div> </NOBR></tD> <tD VALIGN=TOP><NOBR><div>  • IT IS BEST USED IN POWDERED GRAPE DRINK MIXES</div> <div>  • IT CANNOT BE USED TO SWEETEN BABY FOODS, </div> <div>    INFANT DRINKS OR CANDYS MADE WITH CHOCOLATE.</div> <div>  • IT CANNOT BE USED IN BAKED GOODS UNLESS IT IS PART</div> <div>     OF A PRECOOKED FRUIT PECTIN PRESERVE.</div> <div>  • IT IS NOT TO BE USED WITH VEGETABLES,</div> <div>    OR AS A SWEETENER FOR SUPPLEMENTS</div> <div>    WITH ANY VITAMIN A's OR VITAMIN B's BECAUSE,</div> <div>    IT CAUSES, EYE & GASTRO-INTESINAL PROBLEMS .</div> </NOBR></tD> </tR> </TABLE></div> <div>   </div> <DIV ALIGN="LEFT"></DIV> <div>   THIS INFORMATION WAS COMPILED BY<A HREF="http://www.chem-data.com" TARGET="_top" TITLE="http://www.chem-data.com"><U> CHEM-DATA.COM</U></A></div> <div> YOUR SOURCE FOR PERIODIC TABLES IN ALL SIZES</div> <div> <A HREF="ribulose_m.htm" TITLE="CONCORD GRAPE SUGAR RIBULOSE"><U>BACK TO TOP</U></A></div> </NOBR></tD> </tR> </TABLE></div> <bR> <bR> </td> </tr></table></body>