Patient First since Oct 2009
Physician
Mark A. Paster, M.D. since Mar 2009
Physician
Education:
Eastern Virginia Medical School 1996 - 2000
Old Dominion University 1992 - 1996
BS, Biology
Ramapo HS
Skills:
Healthcare Medicine Board Certified Healthcare Management Family Medicine Physicians Clinical Research Urgent Care Medical Education Hospitals Primary Care Public Speaking Managed Care Emergency Medicine Internal Medicine Emr Health Patient Education Social Media Sports Medicine Pediatrics Physician Relations Public Health Teaching Inpatient Critical Care Ehr Healthcare Information Technology Clinical Healthcare Consulting Working With Physicians
Name / Title
Company / Classification
Phones & Addresses
Mark Paster Information Technology Officer
Association of Organ Health and Allied Services
1364 Beverly Rd Ste 100, Mc Lean, VA 22101
Mark Paster Director Information Technology, Information Technology Officer
Association of Organ Health/Allied Services
1364 Beverly Rd, Mc Lean, VA 22101 8500 Leesburg Pike, Vienna, VA 22182 7035564242
Mark Aaron Paster
Mark Paster MD Family Doctor
6862 Elm St, Mc Lean, VA 22101 7032883750
Mark Paster
Patient First Health and Allied Services, Nec, Nsk · Health/Allied Services · Urgent Care Center · Internist
6311 Richmond Hwy, Alexandria, VA 22306 7037682439, 7036476087
Mark A. Paster Owner
Partnermd Medical Doctor's Office
6862 Elm St, Mc Lean, VA 22101
Us Patents
Process For The Preparation Of 3,3-Dimethylbutanal
Jerry R. Ebner - St. Charles MO Zhi Guo - Chicago IL Arnold Hershman - St. Louis MO Loraine M. Klein - Streamwood IL William D. McGhee - Fenton MO Mark D. Paster - Chesterfield MO Indra Prakash - Hoffman Estates IL
Assignee:
The Nutrasweet Company - Mt. Prospect IL
International Classification:
C07C 4500
US Classification:
568449, 568450, 568471, 568850
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethylbutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and sulfuric acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hvdrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converting 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.
Process For The Preparation Of 3,3-Dimethylbutanal
Jerry R. Ebner - St. Charles MO Zhi Guo - Chicago IL Arnold Hershman - St. Louis MO Loraine M. Klein - Streamwood IL William D. McGhee - Fenton MO Mark Paster - Chesterfield MO Indra Prakash - Hoffman Estates IL
Assignee:
The Nutrasweet Company - Mt. Prospect IL
International Classification:
C07C 4529
US Classification:
568449, 450471, 450840
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethylbutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and a mineral acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hydrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converting 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.
Process For The Preparation Of 3,3-Dimethylbutanal
Jerry R. Ebner - St. Charles MO, US Zhi Guo - Chicago IL, US Arnold Hershman - St. Louis MO, US Loraine M. Klein - Streamwood IL, US William D. McGhee - Fenton MO, US Mark Paster - Chesterfield MO, US Indra Prakash - Hoffman Estates IL, US
Assignee:
The Nutrasweet Company - Norwalk CT
International Classification:
C07C 27/00
US Classification:
568876, 568877
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethylbutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and a mineral acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hydrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converting 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.
Process For The Preparation Of 3,3-Dimethylbutanal
Jerry R. Ebner - St. Charles MO, US Zhi Guo - Chicago IL, US Arnold Hershman - St. Louis MO, US Loraine M. Klein - Streamwood IL, US William D. McGhee - Fenton MO, US Mark D. Paster - Chesterfield MO, US Indra Prakash - Hoffman Estates IL, US
Assignee:
The Nutrasweet Company - Mt. Prospect IL
International Classification:
C07C 45/29
US Classification:
568449, 568450
Abstract:
3,3-Dimethylbutanal is prepared from 3,3-dimethybutanol. Intermediate 3,3-dimethylbutanol is obtained by reacting ethylene, isopropylene and a mineral acid to produce a 3,3-dimethylbutyl ester which is hydrolyzed to the alcohol. The hydrolysis step is effectively carried out by reactive distillation. Alternatively, 3,3-dimethylbutanal is prepared from 3,3-dimethylbutanol obtained by reduction of the corresponding carboxylic acid or 1,2-epoxy-3,3-dimethylbutane, or by hydrolysis of 1-halo-3,3-dimethylbutane. Fixed bed gas phase and stirred tank liquid phase processes are provided for converted 3,3-dimethylbutanol to 3,3-dimethylbutanal by catalytic dehydrogenation.
High Temperature Pha Extraction Using Pha-Poor Solvents
Devdatt L. Kurdikar - Maryland Heights MO Fred E. Strauser - St. Charles MO A. John Solodar - University City MO Mark D. Paster - Chesterfield MO
Assignee:
Monsanto Company - St. Louis MO
International Classification:
C08F 600
US Classification:
528480
Abstract:
Polyhydroxyalkanoate (PHA) polyester is extracted from biomass by dissolving the PHA in a non-halogenated solvent which comprises a PHA-poor solvent that dissolves less than 1% of the PHA at temperatures less than the solvent boiling point, or a mixture of a PHA-poor solvent and a PHA-good solvent. Following extraction of PHA under pressure at a temperature above about 80. degree. C. , typically above the boiling point of the PHA-poor solvent, PHA polymer is precipitated by cooling the PHA-enriched solvent mixture. Suitable PHA-poor solvents can include linear and branched R. sub. 1 --OH alcohols and R. sub. 2 --COOR. sub. 3 esters where R. sub. 1 =C. sub. 1 -C. sub. 4, R. sub. 2 =H, C. sub. 1,C. sub. 2, or C. sub. 3, and R. sub. 3 =C. sub. 1 -C. sub. 5.
William D. McGhee - Bridgeton MO Mark D. Paster - Chesterfield MO Dennis P. Riley - Ballwin MO Kenneth W. Ruettimann - St. Louis MO A. John Solodar - University City MO Thomas E. Waldman - Chesterfield MO
Assignee:
Monsanto Company - St. Louis MO
International Classification:
C07C26304
US Classification:
560345
Abstract:
A process for preparing isocyanates comprising contacting carbon dioxide and a primary amine in the presence of an aprotic organic solvent and a base selected from the group consisting of a phosphazene compound, an organic, nitrogenous base and mixtures thereof, wherein the organic, nitrogenous base selected from the group consisting of guanidine compounds, amidine compounds, tertiary amines and mixtures thereof to produce the corresponding ammonium carbamate salt, reacting the ammonium carbamate salt with an anhydride dehydrating agent to produce a product stream comprising the corresponding isocyanate, the aprotic organic solvent and the base salt derived from the anhydride, separating the base salt from the product stream, recovering and recycling the base, and regenerating and recycling the anhydride dehydrating agent.
Methods Of Pha Extraction And Recovery Using Non-Halogenated Solvents
Devdatt L. Kurdikar - Maryland Heights MO Fred E. Strauser - St. Charles MO A. John Solodar - University City MO Mark D. Paster - Chesterfield MO Jawed Asrar - Chesterfield MO
Assignee:
Monsanto Company - St. Louis MO
International Classification:
C12P 742 C12P 762 C12N 120 C08G 6306
US Classification:
435135
Abstract:
Polyhydroxyalkanoate (PHA) polyester is extracted from biomass by dissolving the PHA in a non-halogenated solvent which comprises a PHA-good solvent or a mixture thereof. Suitable PHA-good solvents can be selected from the disclosed alcohols, esters, amides and ketones. The PHA can be recovered, for example, by cooling, by solvent evaporation, or by addition of a PHA-poor solvent, wherein the PHA-poor solvent preferably dissolves less than about 1% (w/v) of the PHA at a temperature below the solvent boiling point. Preferred PHA types for use in the invention are poly (hydroxybutyrate-co-hydroxyvalerate), poly(3-hydroxybutyrate-co-4-hydroxybutyrate), and polymers/copolymers of hydroxyterminated polyhydroxybutyrate.
Medicine Doctors
Dr. Mark A Paster, Laurel MD - MD (Doctor of Medicine)
Healthgrades Honor Roll Washingtonian Magazine Top Doc, 2005
Languages:
English
Hospitals:
3357 Corridor Marketplace, Laurel, MD 20724
x'cel primary care 3357 Corridor Marketplace Suite B, Laurel, MD 20724
x'cel primary care 8105 Ritchie Hwy, Pasadena, MD 21122
x'cel primary care 2855 Crain Hwy, Waldorf, MD 20601
Inova Fairfax Hospital 3300 Gallows Road, Falls Church, VA 22042
Education:
Medical School Eastern Virginia Medical School Of The Medical College Of Hampton Roads Graduated: 2000 Medical School Franklin Square Hospital Center Graduated: 2001 Medical School Franklin Square Hospital Center Graduated: 2003 Medical School Old Dominion University Graduated: 1996