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CAS RN: 6846-35-1 | Product Number: X0001
Xanthane Hydride
Purity: >96.0%(HPLC)
Synonyms:
- ADTT
- 5-Amino-3H-1,2,4-dithiazole-3-thione
- 3-Amino-1,2,4-dithiazole-5-thione
- 5-Imino-5H-[1,2,4]dithiazole-3-thiol
Product Documents:
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Product Number | X0001 |
Purity / Analysis Method | >96.0%(HPLC) |
Molecular Formula / Molecular Weight | C__2H__2N__2S__3 = 150.23 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 6846-35-1 |
Reaxys Registry Number | 112403 |
PubChem Substance ID | 87577871 |
SDBS (AIST Spectral DB) | 3701 |
MDL Number | MFCD00051660 |
Specifications
Appearance | Light yellow to Brown powder to crystal |
Purity(HPLC) | min. 96.0 area% |
Purity(with Total Nitrogen) | min. 96.0 % |
Properties (reference)
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
RTECS# | JO6500000 |
Transport Information:
H.S.code* | 2934.99-000 |
Application
Sulfur-Transfer Reagents for Synthesis of Oligonucleotide Phosphorothioates
References
- Nucleic acid therapeutics: basic concepts and recent developments
- 3H-1,2-Benzodithiol-3-one 1,1-dioxide
- Phosphorothioate Oligonucleotides with Low Phosphate Diester Content: Greater than 99.9% Sulfurization Efficiency with “Aged” Solutions of Phenylacetyl Disulfide (PADS)
- Large-Scale Synthesis of Oligonucleotide Phosphorothioates Using 3-Amino-1,2,4-dithiazole-5-thione as an Efficient Sulfur-Transfer Reagent
- Mechanism of the sulfurisation of phosphines and phosphites using 3-amino-1,2,4-dithiazole-5-thione (xanthane hydride)
Application
Xanthane Hydride: A Sulfur-Transfer Reagent for Synthesis of Oligonucleotide Phosphorothioates
Xanthane hydride (3-amino-1,2,4-dithiazole-5-thione), Beaucage Reagent [B3125] and Bis(phenylacetyl) disulfide [B3623] are used as a sulfur-transfer reagent for synthesis of oligonucleotide phosphorothioates via the phosphoramidite method.1-4) In particular, xanthane hydride has advantages because it does not yield oxidizing substances, carbon disulfide and cyanamide as the additional reaction products.2,3) For DNA/RNA synthesizer, xanthane hydride solution is used, such as 0.02 M solution in acetonitrile/pyridine (9:1),1) or 0.20 M solution in pyridine.4)
References
- 1)Large-Scale Synthesis of Oligonucleotide Phosphorothioates Using 3-Amino-1,2,4-dithiazole-5-thione as an Efficient Sulfur-Transfer Reagent
- 2)Mechanism of the sulfurisation of phosphines and phosphites using 3-amino-1,2,4-dithiazole-5-thione (xanthane hydride)
- 3)Evidence for the formation of isothiocyanate during sulfurisation of phosphines and phosphites using xanthane hydride
- 4)Synthesis of 5’-GalNAc-Conjugated Oligonucleotides: A Comparison of Solid and Solution-Phase Conjugation Strategies
PubMed Literature
Articles/Brochures
TCIMAIL
[Product Highlights] Sulfur-Transfer Reagents for Synthesis of Oligonucleotide PhosphorothioatesProduct Documents (Note: Some products will not have analytical charts available.)
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Specifications
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