[ ] FOR VEB FAHLBERG-LIST IN THE [ ]

• Document Type: CREST
• Collection: General CIA Records
• Document Number (FOIA) /ESDN (CREST): CIA-RDP80-00810A003900200009-8
• Release Decision: RIPPUB
• Original Classification: C
• Document Page Count: 3
• Document Creation Date: December 15, 2016
• Document Release Date: September 8, 2003
• Sequence Number: 9
• Publication Date: April 19, 1954
• Content Type: REPORT

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CENTRAL !NTELLIGENCI AGENCY
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0810A003900200009-8
DATE DST R 19 April
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SUPPLEMENT TO
REPORT NO
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UNEVALUATED INFORM ieee
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The 1953 DDR Economic Plan (Voikewirtschaftsplan 1953) for Research and Technology
the VEB Fahlhergelist cheml.eehe- eel Pharmeeeutische Fabriken, Magdeburg 50,
allotted appropriations for the followitg projects which were to be directed by
'Jr, Elmer Profft. Except where otherwise indicated, all projects required coordtre
with ZAFT (Zentralemt fuer Forschung und Technik) and HV Chemie (Main Administrstioe
for Chemistry),
1, Research on bee-repellents and bee-insecticides. This work was to inelude
attempts to synthesise insecticides harmful to bees and to test the effectivenese
of known agents in various doaages or in various combinations, The work was to
be performed in cooperation with other insecticide manufacturers, particularly
VEB Farbenfabrik Wolfen. Appropriation: 15,000 DRE.
2o Determination of sublethal doses of synthetic 'ontact-iniecttctdes fir insect
pests, The project included the biological measurement of the minieum toxee
dose required to increase the resistance .of the insects. Coordination was
required with the VVP of the inorganic chemical. ielustry and the Siete Secrets
for Chemistry, Minerals and Ores. Appropriation; 15,000 DRE.
Evaluation of C4-derivatives produced by the Reppeesyntheeis in order to determine
their application in pharmaceutical work. Heppe syntheses in acetylene pressure
reactions had produced a (series of by-products which were appropriate intermedietea
for further synthesis.. These by-products were to be investigated and evaluated as
possible starting agents in the synthesis of pharmaceuticals or pharmaeeuticale
intermediates. Other projects included application of the by-products in, the
preparation of pyrrolidine, or other synthesis, and possible applicatien,cr a
recently discovered method for histamine synthesie, Appropriation: 50,000 DME?
Further development of Falicainelike anesthetics including pharmacological and
clinical assay of keto-base thio-estere develeped in 1952 from by-products of
saccharine production; further development of the Falicain production procedure;e
preparation of an anesthetic, with strong bectericidal properties, which could be
injected into inflamed tissues for stomatological therapy; also, development of ,
an isotonic solution of Dento-Falicain. Appropriation: 70,000 DME,
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5, 3yuthesie and testing of sympathcoimetic agents of the adrenalin,sphadrin group?
vaTk concerned preparation or sympathomimetically-active compounas,
'!Artil:171,7 those with a hydrogenated central Pore; developTleht of lobNiin-related
substances originating a3 by-products in the synthesis of ephedrine; development
ot n procedure readily applicable to tho commerciai production of l- and d-
,vhedrine. All compounds were to be pharmaoologicaIly tested, Appropriation;
i0,000 DiE
6, Completion of work on spasmolvtic oompounds with strong muscu/otropic and noun,-
tropic action as well as analgesic proporties. The purpose of the project war to
attain the most effeethe, non-habit forming analgesic from coapounds such as the
oentrally substituted? aryl-aliphatic secondarpand tertiary c=inee. Approprimtiong
30,000 DME,
7? Synthesis and testing of anti-coagulants of the au/roasted pectin. grou! , Turnip
pectin, the material under consideration, Was to be sulfonatA aud.purifiedo The
products were to be tested for their prophylaotic end therapeutic lalue in thrombosis.
ATpropriattong 10,000 D.
8, Synthesis of neurotropic? arsenio-containing? specialized. pharmaceuticals, involvinF
the preparation of a fat-soluble, arsenic compound with oentral nervous System
ar1im1 ty0 lilac, methods were to be dsveiooed for the preparation of Sodiurao, l'yo-
ond Solu,Arsoluin. Phamtcological an41, possibly, clinica/ tests were to be
porrormed on these products propriation.: 70,000 DAE,
Prepaatton of mettl-freo odenticides as a bstitute matal-contelning noisons,
New products witb, greater activity, su'eh. as r,...ryeoumarin or oveoumarin-condensation
produots, were to be obtained from native raw materials, The oxyconmaria prepare-
? os mere to be biologically testelk, Appropriation; 25,000 PME
Inyeatlgetion of fluorine-containing, 'vet-r!outrol aqe.nts. The ut)rk was to
.nt-dudot improvement of metirgAs cor thn IrtiliAstion of taargate wood-protection
? oductal production of new 117$seeticides, fungicides, betoterieldes and
roJanticide thro-4gh tho Introduotion of hydroven fluoride or fluorine derivatives
4I-Ao olganie compounds; augaentation of the Zungicida1 activity of brown and biack
? l-tar oils with fluoro-organie eombinstions improvemnt of the persistence
? iasecticidal action of wood proteetion agents by addition of hydrogen fluoride;
oroduction. at impregnatio;a agents for cooling towers; developNent of repid test
-hods, based on end use, for-',DurfLng fungitAAial activity; biologica1 investi-
epAions of all the new prodoots, A sub,.e.ontrot for this work? amounting to
--2.0100 WE, was to be giver oto the 'VE D Fluorvorks Dohna, Cooperation with VEB
rberfahrik WOITen vas plenned, Appfopriatioag 100,000 ME%
Ainued dcvelopmant of new insectieAes (51:011AT to the organic ehemieal compounds
t?hlordene, aldrin %I:u1 chlorinated benzene. The project was to imiude
o surrivey e 174* literatwe laboratory synthesis utilizin ati79 rawomatorials.
Attempts were to be made to nToducP) ettewper pest-prevention agents Pome biologi-
Al tests were planned? Appropriation3 60,000 DME,
6yntheeis end testinp of lolize-fr*Ie end iotkac-contatnin radiopaque agents,
laclueking sylIttesis or 3,5-dilodo9 4-pyrldons-N-t1e acid alethanoltne
oriabrodil.) end development of thla .inbctanre for commercial production; synthesis
? hmj.-etod ketocarborylin acid and other compounds for roentgenography of the
doot; continord developwot of brominated anl todinsted 4-hydroAvbenzo1t and
.ttAde AS well AO other substances for retrograde pyelography; preparation.
of 'these substances for bronohisi and engiomr4ial.. radiography; replacement of the
Iodise in the nroduets 107 bromine; phemkicclogical end clinicsIJ: testing of the
4rodnets, Ionization measurmentA were to be utilized in. the work Appropristiong
':000 DML,
?repaTeLtiolz. tnd blolagieel tastioFofsl.reate tor coatrol of nemAtnieeg/ utilizing
Available, cheap, effective proJeots? to be tested accordIng to metbodedesoribed in
liteature The woit V$1.8 to re peTTormeti ir operett.011 with VETS
.?sitentabrik Wolfen. Apprortatiow 12,00U DME,
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14, titAItn?:,Ttion. of hg:g.ar:hiorocyelohernhe rosidnes for preparation of plant-Ty,mteetton
npents. The projoct included symthesta of Ilmse :Cv074-4.
LexemAlorosyelonexaAe isomors and examination of the possibilities Ir tIvbtT
;11mTierer..al U900 Thio woTk was to be done tn cooperation With the iL't
A-pr.Top-dation 90,C00 DME.,
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impolement f;.e the hexachlorocyclohne production process.4 furthez dtvelt
,JP joas tor wwction of ;;Pargua hexechlorocytiohoxane an0 incorpo..m.tton or the
;?vodvAtt into Llarket zreparations; simUificatio of the.pross; improvelmat 3f
mva isomer 4.nd enblmsement of the sativity of thu market prewe,tions.
tests were to h rformed. The work wao to be clon44 In r,xrpr,rnti-n with
KciItv Apprortationg 9D,3(In DME.
l'3.4c,tion or rangiuidesi oacteriados from the by-products of t)?1 e?Igiantt
(e;ws(,11,sai industry substitution af lsss Doisorios ef;ents Zor motal-ooKO?Lintng
N.kieleidss aa conne7 ?cl.dclun tkTes.1 hiologiw) testinr w: these 1.gsnts.
Agents verb to be used in sombetting TAAat diseftess eaolntered In garl,F4PIDgE,
Irult-rmising and egricultvre. Epi s wimi to be 7ilaced on developaent of organic
kavicsi compounds, antibiotics .and sulfur products, Coordination with VED
?Liteinfahrik WoIfen UMA required addition to that with ZEIT and NV Chemis.
Arpropriationg 60,000 W.
:mse,rvation of croo AisinrsctaAs This prolect involvcd the preproxtion of m
LPabetite for the meraury-conTaininR naniversal' disiasotant in order to
substitIte was to be prepared from dozestle naterial,
pi?7;-akdy F,tvototie enhatlyzee. prodwed a prort tn factories, Coopc,ration
f the f4;.t.c.r.f,,,a vas to .7vee tad Biologi(cal teats were to be perfoTmed with
sabstuto nrodusts? Aunrapristiong 80,000 DME,
Dr, Profft mot listed aa director of tblm projet, No ovs.o7;
,qoantcidt.6 tanit
C eoi otU.y to rfltato beetles 5.10h iitj esto
L:4 caiti.attooixifati DDE1,
N6t otherseJ izaAtftrieC
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