CAS 9028-12-0|(R)-Alcohol dehydrogenase

Introduction:Basic information about CAS 9028-12-0|(R)-Alcohol dehydrogenase, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name(R)-Alcohol dehydrogenase
CAS Number9028-12-0Molecular Weight532.119
Density1.2±0.1 g/cm3Boiling Point806.8±65.0 °C at 760 mmHg
Molecular FormulaC31H38ClN5OMelting Point/
MSDSChineseUSAFlash Point441.7±34.3 °C
Symbol
GHS08
Signal WordDanger

Names

NameDehydrogenase, Alcohol(Nicotinamide Adenine Dinucleotide Phosphate)
SynonymMore Synonyms

(R)-Alcohol dehydrogenase BiologicalActivity

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 CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others

Chemical & Physical Properties

Density1.2±0.1 g/cm3
Boiling Point806.8±65.0 °C at 760 mmHg
Molecular FormulaC31H38ClN5O
Molecular Weight532.119
Flash Point441.7±34.3 °C
Exact Mass531.276489
LogP5.89
Vapour Pressure0.0±2.9 mmHg at 25°C
Index of Refraction1.663

Safety Information

Symbol
GHS08
Signal WordDanger
Hazard StatementsH317-H334
Precautionary StatementsP261-P280-P342 + P311
Personal Protective EquipmentEyeshields;Gloves
Hazard CodesXn
Risk Phrases42/43
RIDADRNONH for all modes of transport
WGK Germany3

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
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