N-Acetyl-D-galactosamine - ≥98% , CAS No.14215-68-0

CAS: 14215-68-0 Cat. No.: A111905 Peso molecular: 221.21 Beilstein Registry Number: 4(4)2039 Número EC: 805-263-2
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
2-ACETAMIDO-2-DESOXY-D-GALACTOPYRANOSE | 2-Deoxy-2-Acetamido-Galactose | S11316 | N acetyl d galactosamin | N-[(3R,4R,5R,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide | 2-Acetamido-2-Deoxy-Galactose | CHEBI:28037 | D-GalNAc | EN300-7366607 | S
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
A111905-100mg
2

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 14 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
2-ACETAMIDO-2-DESOXY-D-GALACTOPYRANOSE | 2-Deoxy-2-Acetamido-Galactose | S11316 | N acetyl d galactosamin | N-[(3R, 4R, 5R, 6R)-2, 4, 5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide | 2-Acetamido-2-Deoxy-Galactose | CHEBI:28037 | D-GalNAc | EN300-7366607 | S
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasCC(=O)NC1C(C(C(OC1O)CO)O)O
IUPAC NameN-[(3R,4R,5R,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
InChIKeyOVRNDRQMDRJTHS-KEWYIRBNSA-N
INCHI1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6+,7-,8?/m1/s1
Isómeros SMILES CC(=O)N[C@@H]1[C@H]([C@H]([C@H](OC1O)CO)O)O
Peso molecular 221.21
Beilstein 4(4)2039
Reaxy-Rn 1913591
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1913591&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides - Amino sugars
Direct ParentAcylaminosugars
Alternative Parents N-acyl-alpha-hexosamines  Hexoses  Oxanes  Acetamides  Secondary carboxylic acid amides  Secondary alcohols  Hemiacetals  Polyols  Oxacyclic compounds  Primary alcohols  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Acylaminosugar - N-acyl-alpha-hexosamine - Hexose monosaccharide - Monosaccharide - Oxane - Acetamide - Carboxamide group - Hemiacetal - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Organonitrogen compound - Primary alcohol - Carbonyl group - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as acylaminosugars. These are organic compounds containing a sugar linked to a chain through N-acyl group.
External Descriptors Amino sugars
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ASGR1 Tbio Asialoglycoprotein receptor 1 (30 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FUT10 Tdark Fucosyltransferase 10 (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Cryptosporidium parvum (1150 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptosporidium hominis (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeFechaArticulo
G1805091Certificate of AnalysisFeb 05, 2026 A111905
J1809135Certificate of AnalysisAug 08, 2022 A111905
J1809134Certificate of AnalysisAug 08, 2022 A111905
Propiedades químicas y físicas
Rotación específica [α]85 ° (C=1, H2O)
Punto de fusión (°C)158-162°C
Peso molecular221.210 g/mol
XLogP3-1.700
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass221.09 Da
Monoisotopic Mass221.09 Da
Topological Polar Surface Area119.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity235.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Yanan Wang, Huichao Wei, Keyang Li, Liru Liu, Yingfei Zhu, Xinyuan Wang, Jiahui Yan, Liangmin Yu, Xuefeng Yan, Zhiyu He.  (2023)  Ros-responsive dextran-phenylboronic acid-silibinin nanoparticles for targeting delivery of BAPTA-AM to effectively eliminate calcium overload-mediated inflammatory cascades and mitochondrial apoptosis: Alleviating acute liver injury.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.148283]
2. Shiwei Liu, Shuang Han, Yuzhuo Song, Ruonan Sun, Le Zhao, Chen Yan.  (2023)  Disulfide-Bridged Dendritic Organosilicas-Based Biodegradable Molecularly Imprinted Polymers for Multiple Targeting and pH/Redox-Responsive Drug Release toward Chemical/Photodynamic Synergistic Tumor Therapy.  Advanced Healthcare Materials,  12  (20): (2300184).  [PMID:36943098] [10.1002/adhm.202300184]
3. Liu Jing, Xu Mingze, Zhang Tingsong, Chu Xueying, Shi Kaixi, Li Jinhua.  (2022)  Al/TiO2 composite as a photocatalyst for the degradation of organic pollutants.  ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH,  30  (4): (9738-9748).  [PMID:36063271] [10.1007/s11356-022-22861-9]
4. Chunyan Yang, Zixuan Guan, Xincheng Pang, Zengqi Tan, Xiaomin Yang, Xiang Li, Feng Guan.  (2022)  Desialylated Mesenchymal Stem Cells-Derived Extracellular Vesicles Loaded with Doxorubicin for Targeted Inhibition of Hepatocellular Carcinoma.  Cells,  11  (17): (2642).  [PMID:36078050] [10.3390/cells11172642]
5. Han Xu, Ninghua Fu, Jie Zheng, Muhammad Sohail, Xing Zhang.  (2022)  Mn-doped bimetallic synergistic catalysis boosts for enzymatic phosphorylation of N-Acetylglucosamine/ N-Acetylgalactosamine and their derivatives.  BIOORGANIC CHEMISTRY,      [PMID:35907378] [10.1016/j.bioorg.2022.106041]
6. Yan Ma, Na Gao, Zhichuang Zuo, Shanni Li, Wenqi Zheng, Xiang Shi, Qipei Liu, Ting Ma, Ronghua Yin, Xian Li, Jinhua Zhao.  (2021)  Five distinct fucan sulfates from sea cucumber Pattalus mollis: Purification, structural characterization and anticoagulant activities.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:34246676] [10.1016/j.ijbiomac.2021.07.049]
7. Xiang Shi, Ruowei Guan, Lutan Zhou, Zhichuang Zuo, Xuelin Tao, Pin Wang, Yanrong Zhou, Ronghua Yin, Longyan Zhao, Na Gao, Jinhua Zhao.  (2021)  Structural Characterization and Heparanase Inhibitory Activity of Fucosylated Glycosaminoglycan from Holothuria floridana.  Marine Drugs,  19  (3): (162).  [PMID:33803892] [10.3390/md19030162]
8. Lizhen Chen, Jie Wu, Feng Yan, Huangxian Ju.  (2020)  A facile strategy for quantitative sensing of glycans on cell surface using organic electrochemical transistors.  BIOSENSORS & BIOELECTRONICS,      [PMID:33298337] [10.1016/j.bios.2020.112878]
9. Zhenjun Zhu, Xiuping Dong, Chunhong Yan, Chunqing Ai, Dayong Zhou, Jingfeng Yang, Hui Zhang, Xiaoling Liu, Shuang Song, Hang Xiao, Beiwei Zhu.  (2019)  Structural Features and Digestive Behavior of Fucosylated Chondroitin Sulfate from Sea Cucumbers Stichopus japonicus.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:31464434] [10.1021/acs.jafc.9b04996]
10. Lijing Nan, Jiao Li, Wanjun Jin, Ming Wei, Mengjun Tang, Chengjian Wang, Guiping Gong, Linjuan Huang, Ying Zhang, Zhongfu Wang.  (2019)  Comprehensive quali-quantitative profiling of neutral and sialylated O-glycome by mass spectrometry based on oligosaccharide metabolic engineering and isotopic labeling.  RSC Advances,  (28): (15694-15702).  [PMID:35521403] [10.1039/C9RA01114E]
11. Ruowei Guan, Yuan Peng, Lutan Zhou, Wenqi Zheng, Xixi Liu, Pin Wang, Qingxia Yuan, Na Gao, Longyan Zhao, Jinhua Zhao.  (2019)  Precise Structure and Anticoagulant Activity of Fucosylated Glycosaminoglycan from Apostichopus japonicus: Analysis of Its Depolymerized Fragments.  Marine Drugs,  17  (4): (195).  [PMID:30934713] [10.3390/md17040195]
12. Longyan Zhao, Yujing Qin, Ruowei Guan, Wenqi Zheng, Jikai Liu, Jinhua Zhao.  (2018)  Digestibility of fucosylated glycosaminoglycan from sea cucumber and its effects on digestive enzymes under simulated salivary and gastrointestinal conditions.  CARBOHYDRATE POLYMERS,      [PMID:29455981] [10.1016/j.carbpol.2018.01.029]
13. Dong Yang, Xinchuan Zheng, Ning Wang, Shijun Fan, Yongjun Yang, Yongling Lu, Qian Chen, Xin Liu, Jiang Zheng.  (2016)  Kukoamine B promotes TLR4-independent lipopolysaccharide uptake in murine hepatocytes.  Oncotarget,      [PMID:27542278] [10.18632/oncotarget.11292]
14. Yao Wang, Lijing Ye, Ruikun Yan, Haibo Zhou, Guojun Zhao.  (2025)  Ilex asprella polysaccharides alleviate liver injury via antioxidative, anti-inflammatory, and gut microbiota modulating effect.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40081689] [10.1016/j.ijbiomac.2025.142024]
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