D-(-)-Tartaric acid - 10mM in DMSO , CAS No.147-71-7

CAS: 147-71-7 Cat. No.: D421725 Molecular Weight: 150.09 Beilstein Registry Number: 1725145 EC Number: 205-695-6
AVAILABLE TO ORDER
GRADE & PURITY 10mM in DMSO
Synonyms
(2R/S,3R/S)-dihydroxy-1,4-butanedioic acid | AM20080237 | DL-Tartaric acid, >=99% | s3134 | (S,S)-Tartaric acid;Tartaric acid;D-(-)-Tartaric acid | Butanedioic acid, 2,3-dihydroxy-, (S-(R*,R*))- | (2s, 3s)-tartaric acid | Acetamide, N-(5,6,7,8-tetrahydro-
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1ml
D421725-1ml
1

$50.90

$74.90
Save $24.00 (32.04%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 23 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

D-(-)-Tartaric acid is a polyhydroxy acid. Oxidation of d-tartaric acid has been reported.Crystal structure of D-(-)-tartaric acid has been studied by X-ray and neutron diffraction.Tartaric acid is reported to be one of the constituents of soy bean Lipositol.Tartaric acid assists in the generation Y2O3:Eu3+ nanoparticles by solgel method.Tartaric acid is the main acid present in grapes and red wine.
D-(-)-Tartaric acid may be used in the synthesis of the HIV-protease inhibitor nelfinavir.It may be used in the synthesis of chiral aziridine derivative, a common intermediate for the synthesis of hydroxyethylamine class HIV protease inhibitors such as saquinavir, amprenavir, or nelfinavir.

product description:

Tartaric acid is a polyhydroxy acid with wide applications in the textile, pharma, and food industries. It is commonly used as a food additive and acts as an antioxidant and acidification agent. It is also used as a starting material for the preparation of many bioactive molecules.

application:

D-(-)-Tartaric acid is used as a resolving agent in organic synthesis. It is used as a precursor for the preparation of its ester derivatives like D-tartaric acid diethyl ester, D-tartaric acid dimethyl ester and D-tartaric acid diiso-propyl ester. It finds application in the synthesis of chiral aziridine derivative, a common intermediate for the preparation of hydroxyethylamine class HIV protease inhibitors viz. as saquinavir, amprenavir and nelfinavir. It is widely used in the food industry as a beer foaming agent, for food acidity regulations and as a flavoring agent.

Specifications

Synonyms
(2R/S, 3R/S)-dihydroxy-1, 4-butanedioic acid | AM20080237 | DL-Tartaric acid, >=99% | s3134 | (S, S)-Tartaric acid;Tartaric acid;D-(-)-Tartaric acid | Butanedioic acid, 2, 3-dihydroxy-, (S-(R*, R*))- | (2s, 3s)-tartaric acid | Acetamide, N-(5, 6, 7, 8-tetrahydro-
Specifications & Purity
10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesC(C(C(=O)O)O)(C(=O)O)O
IUPAC Name(2S,3S)-2,3-dihydroxybutanedioic acid
InChIKeyFEWJPZIEWOKRBE-LWMBPPNESA-N
INCHI1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m0/s1
Isomeric SMILES [C@H]([C@@H](C(=O)O)O)(C(=O)O)O
WGK Germany 3
RTECS WW7875000
Molecular Weight 150.09
Beilstein 1725145
Reaxy-Rn 510169
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=510169&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
ClassOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Not available
Direct ParentSugar acids and derivatives
Alternative Parents Short-chain hydroxy acids and derivatives  Beta hydroxy acids and derivatives  Monosaccharides  Fatty acids and conjugates  Dicarboxylic acids and derivatives  Alpha hydroxy acids and derivatives  Secondary alcohols  1,2-diols  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Beta-hydroxy acid - Short-chain hydroxy acid - Sugar acid - Monosaccharide - Hydroxy acid - Dicarboxylic acid or derivatives - Alpha-hydroxy acid - Fatty acid - Secondary alcohol - 1,2-diol - Carboxylic acid - Carboxylic acid derivative - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
External Descriptors tartaric acid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MT2 (2907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
pol Human immunodeficiency virus type 1 integrase (9041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HD1 Histone deacetylase (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

1 results found

Lot NumberCertificate TypeDateItem
J2215003Certificate of AnalysisMay 11, 2026 D421725
Chemical and Physical Properties
SensitivityLight Sensitive
Specific Rotation[α]-12.5 ° (C=5, H2O)
Flash Point(°F)410°F
Flash Point(°C)210℃
Melt Point(°C)166-170°C
Molecular Weight150.090 g/mol
XLogP3-1.900
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass150.016 Da
Monoisotopic Mass150.016 Da
Topological Polar Surface Area115.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity134.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
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
References
1. Ziwei Zheng, Shanshan Qiu, Zhenbo Wei.  (2022)  A Novel Voltammetric Electronic Tongue Based on Nanocomposites Modified Electrodes for the Discrimination of Red Wines from Different Geographical Origins.  Chemosensors,  10  (8): (332).  [PMID:] [10.3390/chemosensors10080332]
2. Hui Peng, Faqiang Wang, Danyang Wang, Shuzhen Cui, Wenbo Hou, Guofu Ma.  (2022)  In Situ Self-Anchored Growth of MnO2 Nanosheet Arrays in Polyaniline-Derived Carbon Nanotubes with Enhanced Stability for Zn–MnO2 Batteries.  ACS Applied Energy Materials,      [PMID:] [10.1021/acsaem.2c00360]
3. Xie Qingqiao, Zhuang Yuandi, Ye Gaojun, Wang Tiankuo, Cao Yi, Jiang Lingxiang.  (2021)  Astral hydrogels mimic tissue mechanics by aster-aster interpenetration.  Nature Communications,  12  (1): (1-9).  [PMID:34257316] [10.1038/s41467-021-24663-y]
4. Xie Qingqiao, Chen Xixi, Wu Tianli, Wang Tiankuo, Cao Yi, Granick Steve, Li Yuchao, Jiang Lingxiang.  (2019)  Synthetic asters as elastic and radial skeletons.  Nature Communications,  10  (1): (1-10).  [PMID:31672981] [10.1038/s41467-019-13009-4]
5. Dan-Dan Zhai, Zhen Fang, Hongwei Jin, Ming Hui, Christopher Joseph Kirubaharan, Yang-Yang Yu, Yang-Chun Yong.  (2019)  Vertical alignment of polyaniline nanofibers on electrode surface for high-performance microbial fuel cells.  BIORESOURCE TECHNOLOGY,      [PMID:31128545] [10.1016/j.biortech.2019.121499]
6. Wanru Wang, Weifeng Xu, Guilin Dai, Panliang Zhang, Kewen Tang.  (2018)  Process optimization of reactive extraction of clorprenaline enantiomers by experiment and simulation.  Chemical Engineering and Processing-Process Intensification,      [PMID:] [10.1016/j.cep.2018.10.021]
7. Lingli Zhang, Peng Fu, Boya Wang, Minying Liu, Qingxiang Zhao, Xinchang Pang, Zhe Cui.  (2018)  Preparation of novel optically active polyamide@silica hybrid core-shell nanoparticles and application for enantioselective crystallization.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2018.08.004]
8. Wensheng Tan, Renjun Fu, Hong Ji, Datong Wu, Yueguo Xu, Yong Kong.  (2018)  Comparison of supercapacitive behaviors of polyaniline doped with two low-molecular-weight organic acids: D-tartaric acid and citric acid.  ADVANCES IN POLYMER TECHNOLOGY,  37  (8): (3038-3044).  [PMID:] [10.1002/adv.21974]
9. Lingli Zhang, Chenxi Zhang, Wenjie Zhang, Zhe Cui, Peng Fu, Minying Liu, Xinchang Pang, Qingxiang Zhao.  (2018)  Optical Activity of Homochiral Polyamides in Solution and Solid State: Structural Function for Chiral Induction.  ACS Omega,      [PMID:31458541] [10.1021/acsomega.7b01963]
10. Shenzhi Lai, Shaotan Tang, Jiaqi Xie, Changqun Cai, Xiaoming Chen, Chunyan Chen.  (2017)  Highly efficient chiral separation of amlodipine enantiomers via triple recognition hollow fiber membrane extraction.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:28222860] [10.1016/j.chroma.2017.02.018]
11. Chao Ding, Weili Wei, Hanjun Sun, Jinhua Ding, Jinsong Ren, Xiaogang Qu.  (2014)  Reduced graphene oxide supported chiral Ni particles as magnetically reusable and enantioselective catalyst for asymmetric hydrogenation.  CARBON,      [PMID:] [10.1016/j.carbon.2014.08.022]
12. Zhou Long, Jia Jia, Shanling Wang, Lu Kou, Xiandeng Hou, Michael J. Sepaniak.  (2013)  Visual enantioselective probe based on metal organic framework incorporating quantum dots.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2013.08.013]
13. Lan Yang, Junyu Zhao, Chengyang Wang, Ruotong Pang, Daming Wang, Xiaogang Zhao, Chunhai Chen.  (2024)  Enhanced Thermal Conductivity in Poly(ether imide)-Based Composites via Constructing Microscopic Segregated Networks with Ag-Bridged Graphite Nanoplatelets.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c01813]
14. Lan Yang, Junyu Zhao, Chengyang Wang, Ruotong Pang, Daming Wang, Xiaogang Zhao, Chunhai Chen.  (2024)  Significant enhancement of bi-directional ultrahigh thermal conductivity in polymer composites fabricated via Polyetherimide@Silver core–shell structured microspheres.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.156405]
15. Duo Xu, Bowen Du, Yantian Ji, Huimin Sun, Tiecheng Wang, Xianqiang Yin.  (2024)  Stereoselective transport of 2-aryl propionic acid enantiomers in porous media subjected to chiral organic acids.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:38377915] [10.1016/j.jhazmat.2024.133824]
16. Jialuo Zhang, Ying Li, Dongdong Ding, Enke Feng, Jianjian Ren, Tiaobin Zhao, Zhiming Yang, Zhiqiang Wu.  (2025)  Polyaniline reinforced multifunctional gel for strain sensor with multiple environmental adaptability.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.138468]
17. Detao Li, Zichen Ning, Feiqiang He, Zhi Gao, Limin Zhou, Li Xu, Zhijian Zheng, Jerry Heng, Shichao Du, Jinbo Ouyang.  (2025)  Competitive Chiral Cocrystallization Inspired Enantioseparation: Mechanistic Insights into R/S-Mandelic Acid and d/l-Prolinamide.  CRYSTAL GROWTH & DESIGN,      [PMID:] [10.1021/acs.cgd.5c00692]
18. Rui Gao, Changlong Hao, Liguang Xu, Xinxin Xu, Jing Zhao, Maozhong Sun, Qing Wang, Hua Kuang, Chuanlai Xu.  (2023)  Near-Infrared Chiroptical Activity Titanium Dioxide Supraparticles with Circularly Polarized Light Induced Antibacterial Activity.  ACS Nano,      [PMID:38112427] [10.1021/acsnano.3c08791]
19. Rongxiu Qin, Haiyan Chen, Rusi Wen, Guiqing Li, Zhonglei Meng.  (2023)  Effect of Boric Acid on the Ionization Equilibrium of α-Hydroxy Carboxylic Acids and the Study of Its Applications.  MOLECULES,  28  (12): (4723).  [PMID:37375278] [10.3390/molecules28124723]
20. Panliang Zhang, Shichuan Wang, Weifeng Xu, Kewen Tang.  (2017)  Modeling Multiple Chemical Equilibrium in Single-Stage Extraction of Atenolol Enantiomers with Tartrate and Boric Acid as Chiral Selector.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/acs.jced.7b00698]
21. Muye Yang, Zhengbin Wang, Lingli Zhang, Jingli Wang, Xin Li, Wenjie Zhang, Wei Zhao, Ge Shi, Yanjie He, Yuancheng Zhang, Xiaomeng Zhang, Peng Fu, Zhe Cui, Xinchang Pang, Minying Liu.  (2025)  Tartaric Acid-based Chiral Polyamides: Unraveling Intrinsic Multicolor Clusteroluminescence and Solvent-modulated Emission Mechanism.  Journal of Materials Chemistry C,      [PMID:] [10.1039/D5TC00270B]
22. Biao-Feng Zeng, Canyu Yan, Ye Tian, Yuxin Yang, Long Yi, Shiyang Fu, Xu Liu, Cuifang Kuang, Longhua Tang.  (2025)  Profiling Hydrogen-Bond Conductance via Fixed-Gap Tunnelling Sensors in Physiological Solution.  Chemosensors,  13  (10): (360).  [PMID:] [10.3390/chemosensors13100360]
23. Simin Cheng, Binqian Zhou, Fan Fang, Yunxiang Zhang, Wei Chen, Haodong Tang, Jun Tang, Xiaoqian Xu, Yiwen Li, Jiaji Cheng, Junjie Hao.  (2026)  Chiral Vanadium Oxide Nanostructures for H2O2 Sensing.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.5c05877]
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.