CAS 38864-21-0|N,N',N''-Triacetylchitotriose
| Common Name | N,N',N''-Triacetylchitotriose | ||
|---|---|---|---|
| CAS Number | 38864-21-0 | Molecular Weight | 627.593 |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 1146.9±65.0 °C at 760 mmHg |
| Molecular Formula | C24H41N3O16 | Melting Point | 271-272ºC dec. |
| MSDS | USA | Flash Point | 647.4±34.3 °C |
Names
| Name | N,N’,N’’-Triacetyl Chitotriose |
|---|---|
| Synonym | More Synonyms |
N,N',N''-Triacetylchitotriose BiologicalActivity
| Description | N,N',N''-Triacetylchitotriose, a competitive inhibitor of lysozyme[1]. |
|---|---|
| Related Catalog | Research Areas >>InfectionSignaling Pathways >>Others >>Others |
| References | [1]. T Arvinte, et al. Lysozyme-induced fusion of liposomes with erythrocyte ghosts at acidic pH. Proc Natl Acad Sci U S A. 1986 Feb;83(4):962-6. |
Chemical & Physical Properties
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 1146.9±65.0 °C at 760 mmHg |
| Melting Point | 271-272ºC dec. |
| Molecular Formula | C24H41N3O16 |
| Molecular Weight | 627.593 |
| Flash Point | 647.4±34.3 °C |
| Exact Mass | 627.248657 |
| PSA | 303.13000 |
| LogP | -2.67 |
| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
| Index of Refraction | 1.606 |
| InChIKey | LRDDKCYRFNJZBX-WHFMPQCRSA-N |
| SMILES | CC(=O)NC(C=O)C(O)C(OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2NC(C)=O)C(O)C1NC(C)=O)C(O)CO |
| Storage condition | −20°C |
| Water Solubility | H2O: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | 24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 29329990 |
Articles27
More Articles| Site-directed selection of oligonucleotide antagonists by competitive elution. Antisense Nucleic Acid Drug Dev. 9(1) , 1-11, (1999) Oligonucleotide ligands that bind a protein or a small molecule of interest are readily isolated by in vitro selection and amplification of rare sequences from combinatorial libraries of sequence-rand... | |
| Kinetic analysis of barley chitinase. Arch. Biochem. Biophys. 344 , 335-342, (1997) The endochitinase from barley is the archetypal enzyme for a large class of plant-derived antifungal chitinases. The X-ray structure was solved previously in our laboratory and a mechanism of action p... | |
| Structure of full-length class I chitinase from rice revealed by X-ray crystallography and small-angle X-ray scattering. Proteins 78(10) , 2295-305, (2010) The rice class I chitinase OsChia1b, also referred to as RCC2 or Cht-2, is composed of an N-terminal chitin-binding domain (ChBD) and a C-terminal catalytic domain (CatD), which are connected by a pro... |
Synonyms
| 2-Acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-D-glucose |
| N,N',N''-Triacetylchitotriose |
| Tri-N-acetylchitotriose |
| GlcNAcβ(1-4)GlcNAcβ(1-4)GlcNAc |
| N,N',N''-Triacetyl Chitotriose |
| D-Glucose, O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1->4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1->4)-2-(acetylamino)-2-deoxy- |
