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E7500

Sigma-Aldrich

meso-Erythritol

≥99% (GC)

Synonyme(s) :

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

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About This Item

Formule linéaire :
HOCH2[CH(OH)]2CH2OH
Numéro CAS:
149-32-6
Poids moléculaire :
122.12
Numéro Beilstein :
1719753
Numéro CE :
205-737-3
Numéro MDL:
MFCD00004710
Code UNSPSC :
12352201
ID de substance PubChem :
24894646
Nomenclature NACRES :
NA.25

Niveau de qualité

200

Pureté

≥99% (GC)

Forme

powder

Sucrosité

0.7 × sucrose

Couleur

white

Point d'ébullition

329-331 °C (lit.)

Pf

118-120 °C (lit.)

Solubilité

H2O: 50 mg/mL, clear, colorless

Température de stockage

−20°C

Chaîne SMILES 

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+

Clé InChI

UNXHWFMMPAWVPI-ZXZARUISSA-N

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Application

Meso-Erythritol (i-Erythritol) is a precursor to the important tanning agent L-erythrulose which can be commercially generated by Gluconobacter oxydans DSM 7145. Meso-Erythritol may be used to support the carbon source growth requirement of Gluconobacter bacteria. It is an aliphatic poly-alcohol used in the chemical analysis of the reactivity of various radicals and radical anions. Meso-Erythritol may be used in encapsulated phase change materials (PCMs) to study its potential use in microelectronics cooling applications. It may be used as a reference compound in purification and analytical procedures developed to test fermentation broths.

Actions biochimiques/physiologiques

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

Autres remarques

To gain a comprehensive understanding of our extensive range of Sugar alcohols for your research, we encourage you to visit our Carbohydrates Category page.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

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Man-Yeon Choi et al.
Journal of economic entomology, 112(2), 981-985 (2018-11-30)
Previous studies have demonstrated various combinations of non-nutritive erythritol and sucrose having detrimental effects on Drosophila suzukii (Matsumura). Fly mortality is likely caused by 1) starvation from feeding on non-metabolizable erythritol; and 2) physiological imbalance with abnormally high osmotic pressure
H Hino et al.
Acta dermato-venereologica, 62(3), 185-191 (1982-01-01)
Keratinocytes were dissociated from normal human adult epidermis with clostridial collagenase, dithio-erythritol and trypsin, and cultured. Immediately after this, no connection was seen between contiguous cells. Ruptured desmosomes, with masses of tonofilaments and distinct attachment plaques were still left on
Freek Spitaels et al.
International journal of systematic and evolutionary microbiology, 64(Pt 4), 1134-1141 (2013-12-26)
Three strains, LMG 27748(T), LMG 27749 and LMG 27882 with identical MALDI-TOF mass spectra were isolated from samples taken from the brewery environment. Analysis of the 16S rRNA gene sequence of strain LMG 27748(T) revealed that the taxon it represents
Karnjapan Janthawornpong et al.
Journal of the American Chemical Society, 135(5), 1816-1822 (2013-01-16)
The MEP pathway, which is absent in animals but present in most pathogenic bacteria, in the parasite responsible for malaria and in plant plastids, is a target for the development of antimicrobial drugs. IspH, an oxygen-sensitive [4Fe-4S] enzyme, catalyzes the
Emmanuel Jean Teinkela Mbosso et al.
Chemistry & biodiversity, 10(2), 224-232 (2013-02-19)
A chemical investigation of the Glyphaea brevis leaves and of the Monodora myristica fruits led to the identification of thirteen compounds, seven linear long-chain aliphatic compounds, 1, 2, 4, 6, and 9-11, three steroids, 3a, 3b, and 7, two triterpenes
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