T2144

N,N′,N′′-Triacetylchitotriose

≥93% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 38864-21-0

Synonym(S): NAG3, Tri(N-acetyl-D-glucosamine), O-[2-Acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)]-O-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)]-2-acetamido-2-deoxy-D-glucopyranose

Select a Size

Pack Size SKU Availability Price
10 MG T2144-10-MG In Stock ₹ 30,623.93

T2144 - 10 MG

₹ 30,623.93

In Stock

Quantity

1

Base Price: ₹ 30,623.93

GST (18%): ₹ 5,512.307

Total Price: ₹ 36,136.237

Quality Level

200

Assay

≥93% (HPLC)

form

powder

impurities

≤8% water (Karl Fischer)

color

white to yellow cast

solubility

water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

storage temp.

−20°C

SMILES string

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

InChI

1S/C24H41N3O16/c1-8(32)25-11(4-28)17(36)21(12(35)5-29)42-24-16(27-10(3)34)20(39)22(14(7-31)41-24)43-23-15(26-9(2)33)19(38)18(37)13(6-30)40-23/h4,11-24,29-31,35-39H,5-7H2,1-3H3,(H,25,32)(H,26,33)(H,27,34)/t11-,12+,13+,14+,15+,16+,17+,18+,19+,20+,21+,22+,23-,24-/m0/s1

InChI key

LRDDKCYRFNJZBX-WHFMPQCRSA-N

Other Options

Image Product Name Manufacturer Price Range
50-248-8209
eMolecules​ Medchem Express / NNN-Triacetylchitotriose / 1mg / 705860743 / HY-135072 / / 38864-21-0 / MFCD00136047 / 627.597 / C24H41N3O16
eMolecules​ ₹ 7,556.66
T2144
N,N′,N′′-Triacetylchitotriose
Sigma Aldrich ₹ 30,623.93
AF56163
38864-21-0 | N,N',N''-Triacetylchitotriose
A2B Chem ₹ 3,850.20 - ₹ 79,827.48

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Description

  • Application: N,N′,N′′-Triacetylchitotriose has been used:as a competitive inhibitor of the enzymatic activity of lysozyme to treat Macrophages to inhibit the constitutively lysozyme production[1]to dock the catalytic cleft of Cel9A (endocellulases)[2]as an inhibitory sugar to access the specificity of labelling with gold complexed lectin[3]
  • Biochem/physiol Actions: N,N′,N′′-Triacetylchitotriose is a chitin oligosaccharide,[4] that promotes lysozyme inhibition.[5] Chitin oligosaccharides are associated with many physiological functions. They are biodegradable and are useful in identifying chitin polysaccharides and associated glycoconjugates.[4]
  • Preparation Note: Prepared by the method of Barker, S.A., et al., J. Chem. Soc., 2218 (1958).
  • Other Notes: To gain a comprehensive understanding of our extensive range of Oligosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Show Difference

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Sigma Aldrich

T2144

≥93% (HPLC)...


Quality Level:
200

Assay:
≥93% (HPLC)

form:
powder

impurities:
≤8% water (Karl Fischer)

color:
white to yellow cast

solubility:
water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

storage temp.:
−20°C

SMILES string:
CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2NC(C)=O)[C@H](O)[C@H]1NC(C)=O)[C@H](O)CO

InChI:
1S/C24H41N3O16/c1-8(32)25-11(4-28)17(36)21(12(35)5-29)42-24-16(27-10(3)34)20(39)22(14(7-31)41-24)43-23-15(26-9(2)33)19(38)18(37)13(6-30)40-23/h4,11-24,29-31,35-39H,5-7H2,1-3H3,(H,25,32)(H,26,33)(H,27,34)/t11-,12+,13+,14+,15+,16+,17+,18+,19+,20+,21+,22+,23-,24-/m0/s1

InChI key:
LRDDKCYRFNJZBX-WHFMPQCRSA-N

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CCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCC

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1S/C54H104O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-52(55)58-49-51(60-54(57)48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)50-59-53(56)47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h51H,4-50H2,1-3H3

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