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Merck
CN

Y0000177

1,2,3,4-丁四醇

European Pharmacopoeia (EP) Reference Standard

别名:

1,2,3,4-赤丁四醇, 内消旋-1,2,3,4-四羟基丁烷, I-赤藓糖醇

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关于此项目

线性分子式:
HOCH2[CH(OH)]2CH2OH
化学文摘社编号:
分子量:
122.12
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1719753
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产品名称

1,2,3,4-丁四醇, European Pharmacopoeia (EP) Reference Standard

InChI

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

SMILES string

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

InChI key

UNXHWFMMPAWVPI-ZXZARUISSA-N

grade

pharmaceutical primary standard

API family

erythritol

manufacturer/tradename

EDQM

bp

329-331 °C (lit.)

mp

118-120 °C (lit.)

application(s)

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

format

neat

storage temp.

2-8°C

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Biochem/physiol Actions

Tas1r3 基因的等位变异影响对该糖醇的行为味道反应,表明它是T1R3 受体配体。

Application

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

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.

Other Notes

Sales restrictions may apply.

Packaging

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

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
Yong-Cheol Park et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 815(1-2), 251-260 (2005-01-18)
In-depth knowledge bases on physiological properties of microbes are required to design a better microbial system at a gene level and to develop an industrially viable process in an optimized scheme. Proteomic analyses of industrially useful microorganisms are particularly important
M Wanke et al.
Acta biochimica Polonica, 48(3), 663-672 (2002-02-09)
Higher plants, several algae, bacteria, some strains of Streptomyces and possibly malaria parasite Plasmodium falciparum contain the novel, plastidic DOXP/MEP pathway for isoprenoid biosynthesis. This pathway, alternative with respect to the classical mevalonate pathway, starts with condensation of pyruvate and

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