(R)-Alcohol dehydrogenase

Modify Date: 2024-01-07 09:52:23

(R)-Alcohol dehydrogenase Structure
(R)-Alcohol dehydrogenase structure
Common Name (R)-Alcohol dehydrogenase
CAS Number 9028-12-0 Molecular Weight 532.119
Density 1.2±0.1 g/cm3 Boiling Point 806.8±65.0 °C at 760 mmHg
Molecular Formula C31H38ClN5O Melting Point N/A
MSDS Chinese USA Flash Point 441.7±34.3 °C
Symbol GHS08
GHS08
Signal Word Danger

 Use of (R)-Alcohol dehydrogenase


(R)-Alcohol dehydrogenase (E.C. 1.1.1.2) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name Dehydrogenase, Alcohol(Nicotinamide Adenine Dinucleotide Phosphate)
Synonym More Synonyms

 (R)-Alcohol dehydrogenase Biological Activity

Description (R)-Alcohol dehydrogenase (E.C. 1.1.1.2) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 806.8±65.0 °C at 760 mmHg
Molecular Formula C31H38ClN5O
Molecular Weight 532.119
Flash Point 441.7±34.3 °C
Exact Mass 531.276489
LogP 5.89
Vapour Pressure 0.0±2.9 mmHg at 25°C
Index of Refraction 1.663

 Safety Information

Symbol GHS08
GHS08
Signal Word Danger
Hazard Statements H317-H334
Precautionary Statements P261-P280-P342 + P311
Personal Protective Equipment Eyeshields;Gloves
Hazard Codes Xn
Risk Phrases 42/43
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles30

More Articles
Efficient one-step production of (S)-1-phenyl-1,2-ethanediol from (R)-enantiomer plus NAD(+)-NADPH in-situ regeneration using engineered Escherichia coli.

Microb. Cell Fact. 11 , 167, (2012)

Candida parapsilosis CCTCC M203011 catalyzes the stereoinversion of (R)-1-phenyl-1,2-ethanediol (PED) through oxidation and reduction. Its NAD(+)-linked (R)-carbonyl reductase (RCR) catalyzes the oxid...

A new strategy to improve the efficiency and sustainability of Candida parapsilosis catalyzing deracemization of (R,S)-1-phenyl-1,2-ethanediol under non-growing conditions: increase of NADPH availability.

J. Microbiol. Biotechnol. 19(1) , 65-71, (2009)

Microbial oxidoreductive systems have been widely used in asymmetric syntheses of optically active alcohols. However, when reused in multi-batch reaction, the catalytic efficiency and sustainability o...

Stereospecificity of ketoreductase domains 1 and 2 of the tylactone modular polyketide synthase.

J. Am. Chem. Soc. 130 , 11598-11599, (2008)

Tylactone synthase (TYLS) is a modular polyketide synthase that catalyzes the formation of tylactone (1), the parent aglycone precursor of the macrolide antibiotic tylosin. TYLS modules 1 and 2 are re...

 Synonyms

1H-Indole-3-propanamide, N-[3-[[3-[(6-chloro-1,2,3,4-tetrahydro-9-acridinyl)amino]propyl]methylamino]propyl]-
N-{3-[{3-[(6-Chloro-1,2,3,4-tetrahydro-9-acridinyl)amino]propyl}(methyl)amino]propyl}-3-(1H-indol-3-yl)propanamide
N-{3-[{3-[(6-chloro-1,2,3,4-tetrahydroacridin-9-yl)amino]propyl}(methyl)amino]propyl}-3-(1H-indol-3-yl)propanamide