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D-(-)-Tartaric acid - reagent grade,99%, high purity , CAS No.147-71-7

  • AR
  • ≥99%
Item Number
T107140
Grouped product items
SKUSizeAvailabilityPrice Qty
T107140-100g
100g
In stock
$9.90
T107140-500g
500g
In stock
$18.90
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All Research Area

Basic Description

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 & PurityAR, ≥99%
Shipped InNormal
GradeAR
Product Description

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.

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

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences
Thyroid stimulating hormone receptor agonistAGONISTALA1963Thyroid stimulating hormone receptorSINGLE PROTEINHomo sapiens

DailyMed: [1]


Thyroid stimulating hormone receptor agonistAGONISTALA1963Thyroid stimulating hormone receptorSINGLE PROTEINHomo sapiens

PubMed: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1

DailyMed: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1

DailyMed: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1

DailyMed: [1]


PubMed: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1

FDA: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1Active site

FDA: [1]


PubMed: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1Integrase active site

EMA: [1]


FDA: [1]


PubMed: [1]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1

PubMed: [1] , [2]


Human immunodeficiency virus type 1 integrase inhibitorINHIBITORALA3471Human immunodeficiency virus type 1 integraseSINGLE PROTEINHuman immunodeficiency virus 1

Other: [1]


PubMed: [1] , [2]


Names and Identifiers

Pubchem Sid504758717
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758717
IUPAC Name (2S,3S)-2,3-dihydroxybutanedioic acid
INCHI InChI=1S/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
InChi Key FEWJPZIEWOKRBE-LWMBPPNESA-N
Canonical SMILES C(C(C(=O)O)O)(C(=O)O)O
Isomeric SMILES [C@H]([C@@H](C(=O)O)O)(C(=O)O)O
WGK Germany 3
RTECS WW7875000
PubChem CID 439655
Molecular Weight 150.09
Beilstein 1725145
Reaxy-Rn 1725145

Certificates

C of A & Other Certificates

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

8 results found

Lot NumberCertificate TypeDateItem
L2420847Certificate of AnalysisJul 27, 2024 T107140
K2302072Certificate of AnalysisNov 09, 2023 T107140
C2201471Certificate of AnalysisMar 04, 2022 T107140
E2304269Certificate of AnalysisMar 04, 2022 T107140
C2201482Certificate of AnalysisMar 03, 2022 T107140
F2215253Certificate of AnalysisMar 03, 2022 T107140
F2215254Certificate of AnalysisMar 03, 2022 T107140
F2215255Certificate of AnalysisMar 03, 2022 T107140

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

Safety and Hazards(GHS)

Pictogram(s) GHS05,   GHS07
Signal Danger
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H318:Causes serious eye damage

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P317:Get emergency medical help.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS WW7875000
Reaxy-Rn 1725145
Merck Index 9068

Related Documents

Citations of This Product(14)

1. 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]
2. 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]
3. 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,  (3): (3854–3862).  [PMID:] [10.1021/acsaem.2c00360]
4. 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]
5. 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]
6. 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,  288  (121499).  [PMID:31128545] [10.1016/j.biortech.2019.121499]
7. 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,  134  (141).  [PMID:] [10.1016/j.cep.2018.10.021]
8. 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,  131  (326).  [PMID:] [10.1016/j.reactfunctpolym.2018.08.004]
9. 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]
10. 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,  (2): (2463–2469).  [PMID:31458541] [10.1021/acsomega.7b01963]
11. 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,  62  (12): (4344–4355).  [PMID:] [10.1021/acs.jced.7b00698]
12. 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,  1490  (63).  [PMID:28222860] [10.1016/j.chroma.2017.02.018]
13. 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,  79  (615).  [PMID:] [10.1016/j.carbon.2014.08.022]
14. 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,  110  (764).  [PMID:] [10.1016/j.microc.2013.08.013]

References

1. 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]
2. 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]
3. 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,  (3): (3854–3862).  [PMID:] [10.1021/acsaem.2c00360]
4. 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]
5. 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]
6. 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,  288  (121499).  [PMID:31128545] [10.1016/j.biortech.2019.121499]
7. 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,  134  (141).  [PMID:] [10.1016/j.cep.2018.10.021]
8. 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,  131  (326).  [PMID:] [10.1016/j.reactfunctpolym.2018.08.004]
9. 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]
10. 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,  (2): (2463–2469).  [PMID:31458541] [10.1021/acsomega.7b01963]
11. 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,  62  (12): (4344–4355).  [PMID:] [10.1021/acs.jced.7b00698]
12. 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,  1490  (63).  [PMID:28222860] [10.1016/j.chroma.2017.02.018]
13. 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,  79  (615).  [PMID:] [10.1016/j.carbon.2014.08.022]
14. 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,  110  (764).  [PMID:] [10.1016/j.microc.2013.08.013]

Solution Calculators