Merck
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A7791

Sigma-Aldrich

N-Acetyl-D-lactosamine

≥98%

All Photos(2)
Synonym(s):
2-Acetamido-2-deoxy-4-O-β-D-galactopyranosyl-D-glucopyranose, β-D-Gal-(1→4)-D-GlcNAc, N-Acetyl-4-O-(β-D-galactopyranosyl)-D-glucosamine, LN
Empirical Formula (Hill Notation):
C14H25NO11
CAS Number:
32181-59-2
Molecular Weight:
383.35
Beilstein:
96808
MDL number:
MFCD00063785
PubChem Substance ID:
24891280
NACRES:
NA.25

Quality Level

100

assay

≥98%

form

powder

optical activity

[α]25/D 27.5 to 32.5 °, c = 0.5% (w/v) in water

technique(s)

thin layer chromatography (TLC): suitable

storage temp.

−20°C

SMILES string

CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O

InChI

1S/C14H25NO11/c1-4(18)15-7-9(20)12(6(3-17)24-13(7)23)26-14-11(22)10(21)8(19)5(2-16)25-14/h5-14,16-17,19-23H,2-3H2,1H3,(H,15,18)/t5-,6-,7-,8+,9-,10+,11-,12-,13?,14+/m1/s1

InChI key

KFEUJDWYNGMDBV-RPHKZZMBSA-N

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Application

N-Acetyl-D-lactosamine is used as a specific lectin target molecule in the identification and differentiation of sugar binding molecules such as the galectins. N-Acetyl-D-lactosamine is used in studies of galactosidase, fucosyltransferase, sialyltransferase, and lectin inhibition.
Useful in studies of galactosidase, fucosyltransferase, sialyltransferase, and lectin inhibition.

Packaging

10 mg in autosample vial

Preparation Note

Synthetic

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

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Review of O-Linked Glycoproteins

O-Linked glycoproteins are usually large proteins with a molecular mass of >200 kDa. Glycosylation generally occurs in high-density clusters and may represent as much as 50-80% of the overall mass.

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