Catalog No: A11GD-1264
Cas No: 1446282-39-8
Properties: Mol. Formula: C13H26O5S, Mol. Weight: 294.41
IUPAC Name: tert-butyl 3-[2-[2-(2-sulfanylethoxy)ethoxy]ethoxy]propanoate
Synonyms: Thiol-PEG3-t-butyl ester, 1446282-39-8, Thiol-PEG3-Boc, THIOL-PEG3-T-BUTYLESTER
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Catalog No: A11GD-1056
Cas No: 249508-40-5
Properties: Mol. Formula: C14H22O4, Mol. Weight: 254.32
IUPAC Name: 2-[2-(2-methoxyethoxy)ethoxy]ethoxymethylbenzene
Synonyms: SCHEMBL10711167, triethylene glycol benzyl methyl ether, 249508-40-5,
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Catalog No: A11GD-1012
Cas No: 55489-58-2
Properties: Mol. Formula: C13H20O4, Mol. Weight: 240.29
IUPAC Name: 2-[2-(2-phenylmethoxyethoxy)ethoxy]ethanol
Synonyms: 55489-58-2, Triethylene Glycol Monobenzyl Ether, 2-(2-(2-(Benzyloxy)ethoxy)ethoxy)ethanol, triethyleneglycolmonobenzyl ether
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| Chemical Name | Uridine-5’-diphospho-2-alkyne-N-acetylgalactosamine |
|---|---|
| Synonyms | UDP-GalNAlk, UDP-2-Alkyne-GalNAc, UDP-2-Alkyne-N-Acetylgalactosamine |
| Molecular Formula | C18H29N3O17P2 (approximate) |
| Molecular Weight | ~645 g/mol |
| CAS No. | N/A — research-grade compound |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Alkyne-modified nucleotide sugar donor substrate for GalNAc-transferases (ppGalNAcTs) and O-GlcNAc transferase (OGT); enables bioorthogonal click chemistry labeling of O-GalNAc glycans and O-GlcNAcylated proteins via copper-catalyzed azide–alkyne cycloaddition (CuAAC); used for glycoproteomic profiling, glycan imaging, and metabolic labeling |
| Chemical Name | Uridine-5’-diphospho-6-azido-6-deoxy-D-galactose, Disodium Salt |
|---|---|
| Synonyms | UDP-6-N3-Gal·2Na, UDP-6-Azido-Galactose Disodium Salt, UDP-GalAz |
| Molecular Formula | C15H21N5O16P2 · 2Na |
| Molecular Weight | 635.28 g/mol (disodium salt) |
| CAS No. | 868141-12-2 (free acid) |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Azido-modified nucleotide sugar donor substrate for β-(1,4)-galactosyltransferases; the C6-azido handle enables bioorthogonal detection via strain-promoted azide–alkyne cycloaddition (SPAAC) and copper-catalyzed azide–alkyne cycloaddition (CuAAC); widely used in GlycoConnect™ antibody–drug conjugate (ADC) technology, glycan remodeling, and glycoproteomic profiling |
10 in stock
| Chemical Name | Uridine-5’-diphospho-6-azido-6-deoxy-D-glucose, Disodium Salt |
|---|---|
| Synonyms | UDP-6-N3-Glc·2Na, UDP-α-6N3-Glucose Disodium Salt, UDP-6-Azido-6-deoxy-D-Glucose Disodium Salt |
| Molecular Formula | C15H21N5O16P2 · 2Na |
| Molecular Weight | 635.28 g/mol (disodium salt) |
| CAS No. | 537039-67-1 |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Azido-modified nucleotide sugar donor substrate for glucosyltransferases; the C6-azido handle enables bioorthogonal detection via copper-catalyzed azide–alkyne cycloaddition (CuAAC) and strain-promoted azide–alkyne cycloaddition (SPAAC); used for selective labeling of 5-hydroxymethylcytosine (5-hmC) in genomic DNA, glycan imaging, and glycoproteomic profiling |
10 in stock
| Chemical Name | Uridine-5’-diphospho-N-azidoacetyl-α-D-galactosamine, Disodium Salt |
|---|---|
| Synonyms | UDP-GalNAz·2Na, UDP-N-Azidoacetylgalactosamine Disodium Salt, UDP-GalNAz Disodium |
| Molecular Formula | C17H24N6Na2O17P2 |
| Molecular Weight | 692.33 g/mol (disodium salt) |
| CAS No. | 653600-61-4 |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Azido-modified analogue of UDP-GalNAc; serves as a substrate for N-acetylgalactosaminyltransferases (ppGalNAc-Ts) enabling metabolic and chemoenzymatic glycan labeling; the azidoacetyl handle permits bioorthogonal conjugation via copper-catalyzed azide–alkyne cycloaddition (CuAAC) and strain-promoted azide–alkyne cycloaddition (SPAAC); widely used in O-GalNAc glycoproteomics, mucin-type glycan imaging, and site-specific antibody–drug conjugate (ADC) construction |
10 in stock
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