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A1269000

L-Arabinitol

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

L-(−)-Arabitol, L-Arabinitol

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About This Item

Fórmula empírica (notación de Hill):
C5H12O5
Número de CAS:
7643-75-6
Peso molecular:
152.15
Beilstein/REAXYS Number:
1720521
MDL number:
MFCD00064290
UNSPSC Code:
41116107
PubChem Substance ID:
329770697
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

arabinitol

manufacturer/tradename

EDQM

mp

101-104 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

SMILES string

OC[C@H](O)C(O)[C@@H](O)CO

InChI

1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m0/s1

InChI key

HEBKCHPVOIAQTA-IMJSIDKUSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

ʟ-Arabinitol EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

related product

Referencia del producto
Descripción
Precios

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number

Lo sentimos, en este momento no disponemos de COAs para este producto en línea.

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Sigma-Aldrich

A5502

Adonitol

Teresa J Stradomska et al.
Journal of medical microbiology, 59(Pt 12), 1490-1496 (2010-08-21)
A non-invasive, non-culture-based method of determining urinary D-/L-arabinitol (D-/L-ARA) ratios was investigated as a tool for the diagnosis of invasive candidiasis in nosocomial paediatric infection cases. The study encompassed 138 children aged 4 days to 16 years (mean ± SD=1.6
Renata Bura et al.
Journal of industrial microbiology & biotechnology, 39(7), 1003-1011 (2012-03-09)
An endophytic yeast, Rhodotorula mucilaginosa strain PTD3, that was isolated from stems of hybrid poplar was found to be capable of production of xylitol from xylose, of ethanol from glucose, galactose, and mannose, and of arabitol from arabinose. The utilization
Tomoyuki Toyoda et al.
Journal of industrial microbiology & biotechnology, 38(9), 1179-1185 (2010-11-18)
D-arabitol production from lactose by Kluyveromyces lactis NBRC 1903 has been studied by following the time courses of concentrations of cell mass, lactose, D: -arabitol, ethanol, and glycerol at different temperatures. It was found that temperature is a key factor
Byoung Hoon Yoon et al.
Biotechnology letters, 33(4), 747-753 (2010-12-04)
Xylose reductase (XR) is a key enzyme in biological xylitol production, and most XRs have broad substrate specificities. During xylitol production from biomass hydrolysate, non-specific XRs can reduce L-arabinose, which is the second-most abundant hemicellulosic sugar, to the undesirable byproduct
Srujana Koganti et al.
Applied microbiology and biotechnology, 90(1), 257-267 (2010-12-04)
Glycerol is a major by-product from biodiesel production, and developing new uses for glycerol is imperative to overall economics and sustainability of the biodiesel industry. With the aim of producing xylitol and/or arabitol as the value-added products from glycerol, 214
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