An N-acetylglucosamine oligosaccharide
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N,N',N''-Triacetylchitotriose

Item No. 20759

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-D-glucose
CAS Number
38864-21-0
Synonyms
  • Tri-N-acetyl-Chitotriose
  • Tri-N-acetyl-D-Glucosamine
Molecular Formula
C24H41N3O16
Formula Weight
627.6
Purity
≥95%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 15 mg/mlPBS (pH 7.2): 3 mg/mlWater: slightly soluble
SMILES
O=C(C)N[C@@H]([C@@](O[C@@]([C@H](O)CO)([H])[C@H](O)[C@H](C=O)NC(C)=O)([H])O[C@@H]1CO)[C@@H](O)[C@@H]1O[C@]2([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2NC(C)=O
InChi Code
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+
InChi Key
LRDDKCYRFNJZBX-WHFMPQCRSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    1 mg

    $55

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    5 mg

    $135

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    10 mg

    $190

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    Product Description

    N,N',N''-Triacetylchitotriose is a triose oligosaccharide derived from chitin, consisting of three N-acetylglucosamine units. It has been shown to scavenge reactive oxygen species and to protect DNA from oxidative damage.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Salgaonkar, N., Prakash, D.y., Nawani, N.N., et al. Comparative studies on ability of N-acetylated chitooligosaccharides to scavenge reactive oxygen species and protect DNA from oxidative damage. Indian J. of Biotechnol. 14(2), 186-192 (2015).

    2. Hao, C., Gao, G., Zhang, Y., et al. Acetylated chitosan oligosaccharides act as antagonists against glutamate-induced PC12 cell death via Bcl-2/Bax signal pathway. Mar. Drugs 13(3), 1267-1289 (2015).