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Y0000177

Erythritol

European Pharmacopoeia (EP) Reference Standard

Sinonimo/i:

meso-Erythritol, 1,2,3,4-Butanetetrol, meso-1,2,3,4-Tetrahydroxybutane, i-Erythritol

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About This Item

Formula condensata:
HOCH2[CH(OH)]2CH2OH
Numero CAS:
149-32-6
Peso molecolare:
122.12
Beilstein:
1719753
Numero MDL:
MFCD00004710
Codice UNSPSC:
41116107
ID PubChem:
329830873
NACRES:
NA.24

Grado

pharmaceutical primary standard

Famiglia di API

erythritol

Produttore/marchio commerciale

EDQM

P. eboll.

329-331 °C (lit.)

Punto di fusione

118-120 °C (lit.)

applicazioni

cleaning products
cosmetics
food and beverages
personal care
pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

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

InChI

1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2/t3-,4+
UNXHWFMMPAWVPI-ZXZARUISSA-N

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Descrizione generale

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.

Applicazioni

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

Azioni biochim/fisiol

Allelic variation of the Tas1r3 gene affects behavioral taste responses to this sugar alcohol, suggesting that it is a T1R3 receptor ligand.

Confezionamento

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

Altre note

Sales restrictions may apply.

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number

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Deepak Ganjewala et al.
Current issues in molecular biology, 11 Suppl 1, i35-i45 (2009-02-06)
Isoprenoids, also known as terpenoids, are biosynthesized by the condensation of the two C5 unit isopentenyl diphosphate (IPP) and isomer dimethylallyl diphosphate (DMAPP). Generally, plants use two separate pathways plastidial Methyl-erythritol-4-phosphate (MEP) and cytosolic acetate-mevalonate (MVA) pathways for formation of
Erythritol: a novel noncaloric sweetener ingredient.
P de Cock
World review of nutrition and dietetics, 85, 110-116 (2000-01-27)
A Banerjee et al.
Natural product reports, 31(8), 1043-1055 (2014-06-13)
Covering: up to February 2014. The methylerythritol 4-phosphate (MEP) pathway is the recently discovered source of isoprenoid precursors isopentenyl diphosphate (IDP) and dimethylallyl diphosphate (DMADP) in most bacteria, some eukaryotic parasites, and the plastids of plant cells. The precursors lead
Hee-Jung Moon et al.
Applied microbiology and biotechnology, 86(4), 1017-1025 (2010-02-27)
Erythritol, a four-carbon polyol, is a biological sweetener with applications in food and pharmaceutical industries. It is also used as a functional sugar substitute in special foods for people with diabetes and obesity because of its unique nutritional properties. Erythritol
Nidhi Singh et al.
Current pharmaceutical design, 13(11), 1161-1177 (2007-04-14)
The 2-C-methyl-D-erythritol-4-phosphate (MEP) pathway for isoprenoid biosynthesis has come under increased scrutiny as a target for novel antimalarial, antibacterial and herbicidal agents. 1-Deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) is a key enzyme of the pathway that catalyzes the rearrangement and nicotinamide adenine
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