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A1269000

L-Arabinitol

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

L-(−)-Arabitol, L-Arabinitol

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About This Item

Empirical Formula (Hill Notation):
C5H12O5
CAS Number:
7643-75-6
Molecular Weight:
152.15
Beilstein:
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

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Adonitol ≥99%

Sigma-Aldrich

A5502

Adonitol

Monika Kordowska-Wiater et al.
Polish journal of microbiology, 61(4), 291-297 (2012-01-01)
L-arabitol is used in the food and pharmaceutical industries. It can be secreted by genetically modified Saccharomyces cerevisiae carrying the genes responsible for pentose metabolism in yeast cells. The process of the biotransformation of L-arabinose to arabitol is highly dependent
Ruth Sánchez-Fresneda et al.
Biochemical and biophysical research communications, 430(4), 1334-1339 (2012-12-25)
Candida albicans exponential yeast cells are able to face environmental challenges by mounting a rapid and efficient "general stress response". Here we show that one of the main components of this response consists of the intracellular protective accumulation of the
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
Quan Wang et al.
Journal of bacteriology, 194(8), 1868-1874 (2012-02-14)
Streptococcus pneumoniae is a major human pathogen associated with many diseases worldwide. Capsular polysaccharides (CPSs) are the major virulence factor. The biosynthetic pathway of D-arabinitol, which is present in the CPSs of several S. pneumoniae serotypes, has never been identified.
Brian Bae et al.
Journal of molecular biology, 402(1), 230-240 (2010-07-27)
L-arabinitol 4-dehydrogenase (LAD) catalyzes the conversion of l-arabinitol into l-xylulose with concomitant NAD(+) reduction. It is an essential enzyme in the development of recombinant organisms that convert l-arabinose into fuels and chemicals using the fungal l-arabinose catabolic pathway. Here we
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