Ammonium tartrate dibasic - ≥98% , CAS No.3164-29-2

CAS: 3164-29-2 Cat. No.: A766775 Peso molecular: 184.15 Beilstein Registry Number: 6120352 Número EC: 221-618-9
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
L-(+)-Tartaric Acid Diammonium Salt | Ammonium Tartrate | Diammonium (2R,3R)-2,3-Dihydroxysuccinate | Diammonium L-(+)-Tartrate | Ammonium tartrate, dibasic | Ammonium L-(+)-tartrate | L-Tartraic acid ammonium salt Butanedioic acid, 2,3-dihydroxy-[R-(R*,R
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100g
A766775-100g
1

14,90US$

24,90US$
Guardar 10,00 US$ (40.16%)
500g
A766775-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

72,90US$

74,90US$
Guardar 2,00 US$ (2.67%)
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

Room temperature,Argon charged Ships Normal 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
L-(+)-Tartaric Acid Diammonium Salt | Ammonium Tartrate | Diammonium (2R, 3R)-2, 3-Dihydroxysuccinate | Diammonium L-(+)-Tartrate | Ammonium tartrate, dibasic | Ammonium L-(+)-tartrate | L-Tartraic acid ammonium salt Butanedioic acid, 2, 3-dihydroxy-[R-(R*, R
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasC(C(C(=O)[O-])O)(C(=O)[O-])O.[NH4+].[NH4+]
IUPAC Namediazanium;2,3-dihydroxybutanedioate
InChIKeyNGPGDYLVALNKEG-UHFFFAOYSA-N
INCHI1S/C4H6O6.2H3N/c5-1(3(7)8)2(6)4(9)10;;/h1-2,5-6H,(H,7,8)(H,9,10);2*1H3
Isómeros SMILES C(C(C(=O)[O-])O)(C(=O)[O-])O.[NH4+].[NH4+]
WGK Alemania 3
Número ONU 3077
Grupo de embalaje III
Peso molecular 184.15
Beilstein 6120352
Reaxy-Rn 13248178
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13248178&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 acids and derivatives
ClaseHydroxy acids and derivatives
SubclassBeta hydroxy acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentBeta hydroxy acids and derivatives
Alternative Parents Short-chain hydroxy acids and derivatives  Monosaccharides  Fatty acids and conjugates  Dicarboxylic acids and derivatives  Secondary alcohols  Carboxylic acid salts  1,2-diols  Carboxylic acids  Organic salts  Organic oxides  Organic nitrogen compounds  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Beta-hydroxy acid - Short-chain hydroxy acid - Fatty acid - Dicarboxylic acid or derivatives - Monosaccharide - 1,2-diol - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Organic nitrogen compound - Organooxygen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alcohol - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

5 results found

Lot NumberCertificate TypeFechaArticulo
C2526289Certificate of AnalysisApr 01, 2025 A766775
C2526290Certificate of AnalysisApr 01, 2025 A766775
C2526312Certificate of AnalysisApr 01, 2025 A766775
C2526353Certificate of AnalysisApr 01, 2025 A766775
C2526360Certificate of AnalysisApr 01, 2025 A766775
Propiedades químicas y físicas
SolubilidadSoluble in water and alcohol.
SensibilidadMoisture sensitive.
Rotación específica [α]33° (C=1,H2O)
Peso molecular184.150 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count1
Exact Mass184.07 Da
Monoisotopic Mass184.07 Da
Topological Polar Surface Area123.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity123.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count2
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Citations of This Product
Referencias
1. Zhaoxue Zhang, Yi Lu, Haipu Li, Nan Zhang, Junfei Cao, Bo Qiu, Zhaoguang Yang.  (2021)  Simultaneous Separation of Sb(III) and Sb(V) by High Performance Liquid Chromatography (HPLC) – Inductively Coupled Plasma – Mass Spectrometry (ICP-MS) with Application to Plants, Soils, and Sediments.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2020.1788049]
2. Hengqian Lu, Haiqin Chen, Xin Tang, Qin Yang, Hao Zhang, Yong Q. Chen, Wei Chen.  (2019)  Ultra Performance Liquid Chromatography–Q Exactive Orbitrap/Mass Spectrometry-Based Lipidomics Reveals the Influence of Nitrogen Sources on Lipid Biosynthesis of Mortierella alpina.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:31525294] [10.1021/acs.jafc.9b04455]
3. Zhuotong Zeng, Xueying Guo, Piao Xu, Rong Xiao, Danlian Huang, Xiaomin Gong, Min Cheng, Huan Yi, Tao Li, Guangming Zeng.  (2018)  Responses of microbial carbon metabolism and function diversity induced by complex fungal enzymes in lignocellulosic waste composting.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:29945088] [10.1016/j.scitotenv.2018.06.102]
4. Yang Jie, Wang Guozeng, Ng Tzi Bun, Lin Juan, Ye Xiuyun.  (2016)  Laccase Production and Differential Transcription of Laccase Genes in Cerrena sp. in Response to Metal Ions, Aromatic Compounds, and Nutrients.  Frontiers in Microbiology,      [PMID:26793186] [10.3389/fmicb.2015.01558]
5. Yizhou Tu, Liqin Han, Xiaolu Ding, Xingqi Zhu, Guizhou Xu, Xianchuan Xie, Qing Zhou, Chendong Shuang, Aimin Li.  (2025)  Degradation of pharmaceuticals and personal care products (PPCPs) in municipal wastewater by white rot fungi: Neutral environment exploitation and degradation mechanisms.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.160794]
6. Lao Jinhua, Chen Jianwen, Hu Dengyan, Zhu Wenbo, Liu Si, Wang Xiucai, Zhou Shaopeng, Xiao Peng, Yu Xinmei, Pan Zhongbin.  (2024)  Enhancing the heterointerface stability of Al2O3/Ba0.5Sr0.5TiO3/Al2O3 composite thin films by adaptive anodizing method under high electric field.  JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS,  35  (34): (1-16).  [PMID:] [10.1007/s10854-024-13922-5]
7. Fei Li, Xia Zhang, Feng Liang, Chen Wang, Pingning Jin, Jing Fan.  (2024)  High stability and reactivity of porous calcium tartrate supported nano zero-valent iron in aerobic environment and alkaline wastewater.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2024.114343]
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