N-Acetyllactosamine

• CAS: 32181-59-2
• Catalog Number: ACM32181592
• Category: Other Products
• Molecular Weight: 383.35
• Molecular Formula: C14H25NO11
• Synonyms: D-Glucose, 2-(acetylamino)-2-deoxy-4-O-beta-D-galactopyranosyl-;Acetyllactosamine
• IUPAC Name: N-[(2R,4R,5S,6R)-2,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]acetamide
• InChI Key: KFEUJDWYNGMDBV-FOTVOWFSSA-N
• Boiling Point: 805.5ºC at 760 mmHg
• Melting Point: 191-192°C
• Flash Point: 441°C
• Density: 1.64 g/cm³
• Solubility: water, 1e+006 mg/L @ 25 °C (est)
• Appearance: White crystalline solid
• Active Content: 95%
• Assay: 0.999
• Exact Mass: 383.14300
• Hazard Statements: Xi: Irritant
• H-Bond Acceptor: 11
• H-Bond Donor: 8
• MDL Number: MFCD00063785
• Packaging: 1 ton
• Physical State: Solid
• Refractive Index: 1.623
• Safety Description: 26-36/37
• Storage Conditions: -20°C

Custom Q&A

What is the product name of the chemical with CAS number 32181-59-2?

The product name is N-Acetyllactosamine.

What are some synonyms for N-Acetyllactosamine?

Some synonyms include Acetyllactosamine and D-Glucose, 2-(acetylamino)-2-deoxy-4-O-beta-D-galactopyranosyl-.

What is the IUPAC name of N-Acetyllactosamine?

The IUPAC name is N-[(2R,4R,5S,6R)-2,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]acetamide.

What is the molecular weight of N-Acetyllactosamine?

The molecular weight is 383.35.

What is the molecular formula of N-Acetyllactosamine?

The molecular formula is C14H25NO11.

What is the boiling point of N-Acetyllactosamine?

The boiling point is 805.5ºC at 760 mmHg.

What is the melting point of N-Acetyllactosamine?

The melting point is 191-192°C.

What is the purity of N-Acetyllactosamine?

The purity is 96%.

What are the typical applications of N-Acetyllactosamine?

It is used as an antimicrobial agent and preservative.

What is the physical state of N-Acetyllactosamine?

The physical state is a solid.

Synthetic Use

Upstream Synthesis Route 1

• 6057-48-3

• 32181-59-2

Reference: [1]Yosizawa
[Tohoku Journal of Experimental Medicine, 1950, vol. 52, p. 145,146]
[2]Kuhn; Kirschenlohr
[Justus Liebigs Annalen der Chemie, 1956, vol. 600, p. 115,123]