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63582

Millipore

D-(+)-Mannose

≥99.0% (sum of enantiomers, HPLC), suitable for microbiology

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Synonym(s):
D-Mannopyranose
Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
3458-28-4
Molecular Weight:
180.16
Beilstein:
1564373
EC Number:
222-392-4
MDL number:
MFCD00064122
PubChem Substance ID:
329759876
NACRES:
NA.85

Quality Level

200

Assay

≥99.0% (sum of enantiomers, HPLC)

form

powder

optical activity

[α]20/D +13.8±0.5°, 24 hr, c = 10% in H2O

ign. residue

≤0.1% (as SO4)

loss

≤0.2% loss on drying, 20 °C (HV)

mp

133-140 °C (lit.)

solubility

H2O: 0.1 g/mL, clear, colorless

application(s)

microbiology

SMILES string

OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6?/m1/s1

InChI key

WQZGKKKJIJFFOK-QTVWNMPRSA-N

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This Item
63580M857463579
D-(+)-Mannose ≥99.0% (sum of enantiomers, HPLC), suitable for microbiology

Millipore

63582

D-(+)-Mannose

D-(+)-Mannose ≥99%, suitable for microbiology

Millipore

63580

D-(+)-Mannose

D-(+)-Mannose synthetic, ≥99%

Sigma-Aldrich

M8574

D-(+)-Mannose

D-(+)-Mannose BioUltra, ≥99.5% (sum of enantiomers, HPLC)

Sigma-Aldrich

63579

D-(+)-Mannose

form

powder

form

powder

form

powder

form

solid

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

mp

133-140 °C (lit.)

solubility

H2O: 0.1 g/mL, clear, colorless

solubility

H2O: 0.1 g/mL, clear, colorless

solubility

water: soluble 10 g/L at 20 °C

solubility

H2O: 1 M, clear, colorless

Quality Level

200

Quality Level

200

Quality Level

-

Quality Level

-

optical activity

[α]20/D +13.8±0.5°, 24 hr, c = 10% in H2O

optical activity

[α]20/D +13.8±0.5°, 24 hr, c = 10% in H2O

optical activity

[α]25/D 13.5 to 14.9 °, c = 4% (w/v) in water

optical activity

[α]20/D +13.8±0.5°, 24 hr, c = 10% in H2O

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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M Otter et al.
Hepatology (Baltimore, Md.), 16(1), 54-59 (1992-07-01)
Various studies have shown that mannose receptors rapidly eliminate glycoproteins and microorganisms bearing high mannose-type carbohydrate chains from the blood circulation. The purpose of this study was to characterize the mannose receptor in the liver, which in vivo is involved
E A Biessen et al.
The Journal of biological chemistry, 271(45), 28024-28030 (1996-11-08)
In search of synthetic high affinity ligands for the mannose receptor, we synthesized a series of lysine-based oligomannosides containing two (M2L) to six (M6L5) terminal alpha-D-mannose groups that are connected with the backbone by flexible elongated spacers (16 A). The
I Adlerberth et al.
Applied and environmental microbiology, 62(7), 2244-2251 (1996-07-01)
Two Lactobacillus plantarum strains of human intestinal origin, strains 299 (= DSM 6595) and 299v (= DSM 9843), have proved to be efficient colonizers of the human intestine under experimental conditions. These strains and 17 other L. plantarum strains were
Chia-Suei Hung et al.
Molecular microbiology, 44(4), 903-915 (2002-05-16)
The first step in the colonization of the human urinary tract by pathogenic Escherichia coli is the mannose-sensitive binding of FimH, the adhesin present at the tip of type 1 pili, to the bladder epithelium. We elucidated crystallographically the interactions
A T Van der Ploeg et al.
The Journal of clinical investigation, 87(2), 513-518 (1991-02-01)
The lysosomal storage disorder glycogenosis type II is caused by acid alpha-glucosidase deficiency. In this study we have investigated the possible applicability of mannose 6-phosphate receptor-mediated enzyme replacement therapy to correct the enzyme deficiency in the most affected tissues. Bovine
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Protocols

HPLC Analysis of Monosaccharides Ribose, Xylitol, and Mannose on Chromolith® NH2

Separation of Ribose, United States Pharmacopeia (USP) Reference Standard; Xylitol, analytical standard; Mannose, United States Pharmacopeia (USP) Reference Standard

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