L-(+)-Arabinose

Suppliers

Names

[ CAS No. ]:
5328-37-0

[ Name ]:
L-(+)-Arabinose

[Synonym ]:
L-(+)-Arabinose
(+)-Arabinose
EINECS 226-214-6
Arabinose
L-arabino-pentose
MFCD00135866
L-Arabinose

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
415.5±38.0 °C at 760 mmHg

[ Melting Point ]:
155ºC

[ Molecular Formula ]:
C5H10O5

[ Molecular Weight ]:
150.130

[ Flash Point ]:
219.2±23.3 °C

[ Exact Mass ]:
150.052826

[ PSA ]:
97.99000

[ LogP ]:
-2.39

[ Vapour Pressure ]:
0.0±2.2 mmHg at 25°C

[ Index of Refraction ]:
1.544

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  •
  • 3-O-β-D-galactopyranosyl-(1->3)-α-L-arabinopyranosylhederagenin 28-O-β-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl ester

DownStream

  • Glyceric Acid
  • Formic Acid
  • L-Arabinoic acid
  • D-(+)-Glyceraldehyde
  • 2,3,4-tri-O-Acetyl-beta-L-arabinopyranosyl bromide
  • Acetoin
  • (2R,3R)-(-)-2,3-Butanediol
  • Ethanol
  • 1,3-Propanediol

Articles

Escherichia coli kduD encodes an oxidoreductase that converts both sugar and steroid substrates.

Appl. Microbiol. Biotechnol. 98(12) , 5471-85, (2014)

A previously unidentified oxidoreductase from Escherichia coli catalyzes the regioselective reduction of eukaryotic steroid hormone 11-deoxycorticosterone (11-DOC) to the valuable bioactive product 4-...

The N terminus of type III secretion needle protein YscF from Yersinia pestis functions to modulate innate immune responses.

Infect. Immun. 83(4) , 1507-22, (2015)

The type III secretion system is employed by many pathogens, including the genera Yersinia, Shigella, Pseudomonas, and Salmonella, to deliver effector proteins into eukaryotic cells. The injectisome n...

Fingerprinting profile of polysaccharides from Lycium barbarum using multiplex approaches and chemometrics.

Int. J. Biol. Macromol. 78 , 230-7, (2015)

Techniques including ultraviolet-visible spectra (UV), high performance size-exclusion chromatography (HPSEC), Fourier-transform infrared spectroscopy (FT-IR) and pre-column derivatization high-perfor...


More Articles

Related Compounds

  • l-(+)-arabinose
  • L-(+)-arabinose
  • L-(+)-Arabinose
  • L-(+)-arabinose
  • L-(+)-Arabinose
  • L-(+)-Arabinose-hydrazon
  • (4-((2,6-Dimethylpyrimidin-4-yl)oxy)piperidin-1-yl)(5-(furan-2-yl)isoxazol-3-yl)methanone
  • 3-(4-((2,6-dimethylpyrimidin-4-yl)oxy)piperidine-1-carbonyl)-1-methylpyridin-2(1H)-one
  • [1,1':4',1'':4'',1'''-Quaterphenyl]-2,2''',4,4'''-tetracarboxylic acid
  • tert-Butyl N-[(3R)-4,4-difluoropyrrolidin-3-yl]carbamate
  • (2S, 4S)-Fmoc-4-(n'-pbf-guanidino)-pyrrolidine-2-carboxylic acid
  • 2-fluoro-5-(1H-1,2,3-triazol-1-yl)aniline hydrochloride
  • 4-[(Diethylamino)methyl]-1,3-thiazol-2-amine hydrochloride
  • 1-Ethyl-2,6-dimethylpiperazine hydrochloride
  • 2-amino-N-(2-methylpyridin-3-yl)propanamide hydrochloride
  • 2-(4-(1,1-Difluoroethyl)piperidin-1-yl)ethan-1-amine
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