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08897

Sigma-Aldrich

D-Erythritol 4-phosphate lithium salt

≥95.0% (TLC)

Synonym(s):

(2R,3S)-2,3,4-Trihydroxybutylphosphate lithium salt, L-Erythritol 1-phosphate lithium salt

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About This Item

Empirical Formula (Hill Notation):
C4H11O7P · xLi+
CAS Number:
7183-41-7
Molecular Weight:
202.10 (free acid basis)
UNSPSC Code:
12352201
NACRES:
NA.25

Assay

≥95.0% (TLC)

form

solid

color

white to off-white

storage temp.

−20°C

SMILES string

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

InChI

1S/C4H11O7P/c5-1-3(6)4(7)2-11-12(8,9)10/h3-7H,1-2H2,(H2,8,9,10)/t3-,4+/m0/s1

InChI key

QRDCEYBRRFPBMZ-IUYQGCFVSA-N

Other Notes

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCBN9928V
BCBM5703V
BCBM5703

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The enantiomorphic erythritol-4-phosphates.
MacDonald, D.L., et al.
Journal of the American Chemical Society, 78, 3720-3722 (1956)
M Veiga-da-Cunha et al.
Journal of bacteriology, 175(13), 3941-3948 (1993-07-01)
It was recently observed that Leuconostoc oenos GM, a wine lactic acid bacterium, produced erythritol anaerobically from glucose but not from fructose or ribose and that this production was almost absent in the presence of O2. In this study, the
Erythritol metabolism by Propionibacterium pentosaceum. The role of L-erythrulose 1-phosphate.
E J Wawszkiewicz
Biochemistry, 7(2), 683-687 (1968-02-01)
Distribution and structural form of phosphate ester groups in commercial starch phosphates.
Gramera, R.E., et al.
Cereal Chem., 43, 104-111 (1966)

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