D-Tagatose - ≥99% , CAS No.87-81-0

CAS: 87-81-0 Cat. No.: D115339 Peso molecular: 180.16 Beilstein Registry Number: 1724555 Número EC: 201-772-3
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
DB04936 | d-lyxo-hexulose | REl-(3S,4S,5R)-1,3,4,5,6-pentahydroxyhexan-2-one | Q414089 | BJHIKXHVCXFQLS-PQLUHFTBSA-N | EINECS 201-772-3 | GEO-02222 | UNII-T7A20Y888Y | AS-44378 | Naturlose | Tagatose, United States Pharmacopeia (USP) Reference Standard |
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250mg
D115339-250mg
3

10,90US$

16,90US$
Guardar 6,00 US$ (35.50%)
1g
D115339-1g
5

16,90US$

25,90US$
Guardar 9,00 US$ (34.75%)
5g
D115339-5g
5

21,90US$

32,90US$
Guardar 11,00 US$ (33.43%)
25g
D115339-25g
3

61,90US$

92,90US$
Guardar 31,00 US$ (33.37%)
100g
D115339-100g
5

193,90US$

290,90US$
Guardar 97,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

📚

Literature proof

Cited in 18 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
DB04936 | d-lyxo-hexulose | REl-(3S, 4S, 5R)-1, 3, 4, 5, 6-pentahydroxyhexan-2-one | Q414089 | BJHIKXHVCXFQLS-PQLUHFTBSA-N | EINECS 201-772-3 | GEO-02222 | UNII-T7A20Y888Y | AS-44378 | Naturlose | Tagatose, United States Pharmacopeia (USP) Reference Standard |
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504756099
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756099
Sonrisas canónicasC(C(C(C(C(=O)CO)O)O)O)O
IUPAC Name(3S,4S,5R)-1,3,4,5,6-pentahydroxyhexan-2-one
InChIKeyBJHIKXHVCXFQLS-PQLUHFTBSA-N
INCHI1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5+,6-/m1/s1
Isómeros SMILES C([C@H]([C@@H]([C@@H](C(=O)CO)O)O)O)O
WGK Alemania 3
RTECS WW1100000
Peso molecular 180.16
Beilstein 1724555
Reaxy-Rn 2207947
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2207947&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 Not available
Direct ParentMonosaccharides
Alternative Parents Beta-hydroxy ketones  Acyloins  Alpha-hydroxy ketones  Secondary alcohols  Polyols  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monosaccharide - Beta-hydroxy ketone - Acyloin - Alpha-hydroxy ketone - Secondary alcohol - Ketone - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as monosaccharides. These are compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn.
External Descriptors tagatose - D-tagatose
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 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.

15 results found

Lot NumberCertificate TypeFechaArticulo
F1218019Certificate of AnalysisMar 06, 2024 D115339
A2408770Certificate of AnalysisNov 25, 2023 D115339
A2408771Certificate of AnalysisNov 25, 2023 D115339
A2408785Certificate of AnalysisNov 25, 2023 D115339
A2408786Certificate of AnalysisNov 25, 2023 D115339
A2408787Certificate of AnalysisNov 25, 2023 D115339
F2316956Certificate of AnalysisJul 15, 2022 D115339
F2316961Certificate of AnalysisJul 15, 2022 D115339
F2316962Certificate of AnalysisJul 15, 2022 D115339
G2313228Certificate of AnalysisJul 15, 2022 D115339
J2228439Certificate of AnalysisJul 15, 2022 D115339
J2228440Certificate of AnalysisJul 15, 2022 D115339
J2228446Certificate of AnalysisJul 15, 2022 D115339
J2228483Certificate of AnalysisJul 15, 2022 D115339
J2228485Certificate of AnalysisJul 15, 2022 D115339

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Propiedades químicas y físicas
SensibilidadHygroscopic
Rotación específica [α]-5.5 ° (C=1, H2O)
Punto de fusión (°C)130-135°C
Peso molecular180.160 g/mol
XLogP3-3.200
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass180.063 Da
Monoisotopic Mass180.063 Da
Topological Polar Surface Area118.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity147.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Ting Zhang, Yuting Li, Xiaoming Lv, Shen Jiang, Shuang Jiang, Zhongqi Sun, Mingxu Zhang, Yang Li.  (2023)  Ultra-Sensitive and Unlabeled SERS Nanosheets for Specific Identification of Glucose in Body Fluids.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202315668]
2. Zihao Wang, Mingming Wang, Xiaomei Lyu, Caiyun Wang, Yanjun Tong, Xiao Hua, Ruijin Yang.  (2022)  Recycling preparation of high-purity tagatose from galactose using one-pot boronate affinity adsorbent-based adsorption-Assisted isomerization and simultaneous purification.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.137089]
3. Haiying Chen, Peiwen Zhou, Chunfang Song, Guangyuan Jin, Lingjun Wei.  (2022)  An approach to manufacturing heat-stable and bloom-resistant chocolate by the combination of oleogel and sweeteners.  JOURNAL OF FOOD ENGINEERING,      [PMID:] [10.1016/j.jfoodeng.2022.111064]
4. Wen-Bin Su, Fei-Long Li, Xue-Yong Li, Xiao-Man Fan, Rui-Jiang Liu, Ye-Wang Zhang.  (2021)  Using galactitol dehydrogenase coupled with water-forming NADH oxidase for efficient enzymatic synthesis of L-tagatose.  New Biotechnology,      [PMID:33460816] [10.1016/j.nbt.2021.01.003]
5. Dongxian Li, Yanyan Zhang, Qingqian Guo, Xiaoquan Sun, Hao Zhang, Shun Wang, Zephania Birech, Jiandong Hu.  (2020)  An efficient LSPR method to quantitatively detect dimethoate: Development, characterization and evaluation.  PLoS One,  15  (9): (e0239632).  [PMID:32970749] [10.1371/journal.pone.0239632]
6. Guo Zongren, Long Liangkun, Ding Shaojun.  (2020)  Characterization of an L-Arabinose Isomerase from Bacillus velezensis and Its Application for L-Ribulose and L-Ribose Biosynthesis.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,  192  (3): (935-951).  [PMID:32617845] [10.1007/s12010-020-03380-0]
7. Guoyan Zhang, Hossain M. Zabed, Junhua Yun, Jiao Yuan, Yufei Zhang, Yang Wang, Xianghui Qi.  (2020)  Two-stage biosynthesis of D-tagatose from milk whey powder by an engineered Escherichia coli strain expressing L-arabinose isomerase from Lactobacillus plantarum.  BIORESOURCE TECHNOLOGY,      [PMID:32105844] [10.1016/j.biortech.2020.123010]
8. Feng Sha, Yucong Zheng, Jiao Chen, Kequan Chen, Fei Cao, Ming Yan, Pingkai Ouyang.  (2018)  D-Tagatose manufacture through bio-oxidation of galactitol derived from waste xylose mother liquor.  GREEN CHEMISTRY,  20  (10): (2382-2391).  [PMID:] [10.1039/C8GC00091C]
9. Chengyu Lu, Ziwei Chen, Yuvaraj Ravikumar, Guoyan Zhang, Xinrui Tang, Yufei Zhang, Mei Zhao, Wenjing Sun, Xianghui Qi.  (2024)  Improving Catalytic Efficiency of L-Arabinose Isomerase from Lactobacillus plantarum CY6 towards D-Galactose by Molecular Modification.  Foods,  13  (11): (1727).  [PMID:38890956] [10.3390/foods13111727]
10. Wenhao Xia, Shimeng Liu, Lihui Huang, Hao Wu, Tao Bai, Shanshan Wang, Fei Hao, Xiao Wang, Wen Wang.  (2024)  Reshaping the binding pocket of D-tagaturonate epimerase UxaE to improve the epimerization activity of C4-OH for enabling green synthesis of d-tagatose.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.114439]
11. Yuanqiang Lv, Jie Chu, Xiaoxiao Zhang, Xuan Li, Aijiao Yin, on behalf of The Industrial Microbiology Laboratory.  (2025)  Synbiotics effects of d-tagatose and Lactobacillus rhamnosus GG on the inflammation and oxidative stress reaction of Gallus gallus based on the genus of cecal bacteria and their metabolites.  PLoS One,  20  (1): (e0317825).  [PMID:39869614] [10.1371/journal.pone.0317825]
12. Fang Shi, Yong-Sheng Gao, Shu-Mei Han, Huan Shi, Qing-Sheng Hou, Yang Gao, Xiao-Wen Wen, Zhen-Yu Zhu, Kai Liu, Wei-Peng Gong, Ben-Shi Wang, Xin Liu, Lei Zou.  (2024)  Targeting MLCK-MLC2 signaling pathway by tagatose alleviates dysregulated mitochondria-associated colonitis.  Journal of Functional Foods,      [PMID:] [10.1016/j.jff.2024.106222]
13. Zepeng Li, Runmin Wang, Xiantai Lai, Wenyi Liao, Runfeng Liao, Zhuohong Wu, Guoyan Zhang, Xianghui Qi.  (2025)  Enabling Stable Recycling of L-Arabinose Isomerase Through Whole-Cell Immobilization for Efficient and Cost-Effective D-Tagatose Production.  Foods,  14  (9): (1538).  [PMID:40361621] [10.3390/foods14091538]
14. Yan Wen, Yan Zhang, Na Lü, Zehui Xuan, Lili Lu.  (2025)  Conversion of D-galactose and guar gum hydrolysate to D-tagatose using L-arabinose isomerase immobilized in sodium alginate-silica hydrogel.  FOOD HYDROCOLLOIDS,      [PMID:] [10.1016/j.foodhyd.2025.111617]
15. Zhou Chen, Yuhan Yan, Ziang Wu, Yanyin Song, Jiangqi Xu.  (2025)  Expression and Characterization of L-Arabinose Isomerase and Its Enzymatic Recycling of the Expired Milk.  Foods,  14  (11): (1873).  [PMID:40509401] [10.3390/foods14111873]
16. Le Wang, Houzhen Lu, Haitao Gui, Zifu Ni, Zhongke Sun, Zihua Wang, Zhihua Wang, Xuanyan Liu, Qipeng Yuan.  (2025)  D-Tagatose attenuates DSS-induced ulcerative colitis by inhibiting inflammation, reducing intestinal barrier damage and modulating the intestinal flora composition.  Food & Function,      [PMID:40528436] [10.1039/D4FO06475E]
17. Yun Liu, Zhina Qiao, Hengwei Zhang, Xian Zhang, Yanan Li, Zhiming Rao.  (2025)  Efficient one-step conversion of low-cost lactose to high-yield D-tagatose in Corynebacterium glutamicum using L-arabinose isomerase.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41475642] [10.1016/j.ijbiomac.2025.149966]
18. Jing Zhang, Liqiang Yan, Huihui Su, Xiaoyang Ou, Tao Xiong, Mingyong Xie, Fei Peng.  (2026)  Construction of dual-enzyme hybrid nanoflowers by protein self-assembly and biomineralization for efficient biosynthesis of d-tagatose.  BIORESOURCE TECHNOLOGY,      [PMID:] [10.1016/j.biortech.2026.134347]
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