Sodium bitartrate monohydrate - UltraBio™, Ultra pure, ≥99%(T) , CAS No.6131-98-2

CAS: 6131-98-2 Cat. No.: S476200 Formula: C4H5NaO6.H2O Peso molecolare: 190.08 Numero EC: 208-400-9 PubChem CID: 23678966
Disponibile su ordine
GRADE & PURITY UltraBio™ ? UltraBio™ — Aladdin's line for molecular-biology applications. Use for nuclease-free, high-consistency reagents across molecular workflows. Ultra pure ? Ultra-pure grade with very low impurity content across the board. Use for trace analysis, electronics, or processes intolerant of contamination. ≥99%(T)
Synonyms
Sodium bitartrate monohydrate | SCHEMBL72547 | sodium 3-carboxy-2,3-dihydroxypropanoate hydrate | L-(+)-Tartaric acid monosodium salt | Sodium bitartrate monohydrate, BioUltra, >=99.0% (T) | A870929 | Sodium 3-carboxy-2,3-dihydroxypropanoate--water (1/1/1
Storage
Room temperature
★
Size
Germania (EU)
USA*
Price
Qty
250g
S476200-250g
Su ordinazione · 8–12 settimane
130,07€
Enter a quantity for the sizes you want to add.
🧪

Why this grade

UltraBio™, Ultra pure, ≥99%(T) Ultra pure,UltraBio™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

L-Tartaric acid (L-(+)-Tartaric acid) sodium hydrate is the enantiomer of D-tartaric acid. L-Tartaric acid is a white crystalline dicarboxylic acid found in many plants, such as grapes, and is one of the main organic acids in wine. L-Tartaric acid sodium hydrate which acts as a flour bulking agent and as a food additive can interact with sodium bicarbonate to produce carbon dioxide.

Specifications

Sinonimi
Sodium bitartrate monohydrate | SCHEMBL72547 | sodium 3-carboxy-2,3-dihydroxypropanoate hydrate | L-(+)-Tartaric acid monosodium salt | Sodium bitartrate monohydrate, BioUltra, >=99.0% (T) | A870929 | Sodium 3-carboxy-2,3-dihydroxypropanoate--water (1/1/1
Specifiche e purezza
UltraBio™, Ultra pure, ≥99%(T)
Condizioni di conservazione di stoccaggio
Room temperature
Grado
Ultra pure, UltraBio™
Purezza
≥99%(T)
Nomi e identificatori
Sorrisi canoniciC(C(C(=O)[O-])O)(C(=O)O)O.O.[Na+]
IUPAC Namesodium;2,3,4-trihydroxy-4-oxobutanoate;hydrate
InChIKeyLLVQEXSQFBTIRD-UHFFFAOYSA-M
INCHI1S/C4H6O6.Na.H2O/c5-1(3(7)8)2(6)4(9)10;;/h1-2,5-6H,(H,7,8)(H,9,10);;1H2/q;+1;/p-1
Isomeri SMILES C(C(C(=O)[O-])O)(C(=O)O)O.O.[Na+]
PubChem CID 23678966
Peso molecolare 190.08

Documentazione

📋 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
ClasseOrganooxygen 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  Carboxylic acid salts  1,2-diols  Carboxylic acids  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Organic cations  
Molecular FrameworkAliphatic acyclic compounds
Substituents Beta-hydroxy acid - Sugar acid - Short-chain hydroxy acid - Alpha-hydroxy acid - Fatty acid - Monosaccharide - Hydroxy acid - Dicarboxylic acid or derivatives - 1,2-diol - Carboxylic acid salt - Secondary alcohol - Organic alkali metal salt - Carboxylic acid derivative - Carboxylic acid - Organic oxide - Alcohol - Organic salt - Carbonyl group - Organic sodium salt - Hydrocarbon derivative - Organic cation - Aliphatic acyclic compound
DescrizioneThis 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 Not available
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Solubilità H2O: 0.1M at20°C, clear, colorless
SensibilitàMoisture sensitive
Peso molecolare190.080 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass190.009 Da
Monoisotopic Mass190.009 Da
Topological Polar Surface Area119.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity157.000
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
Domande frequenti e articoli
Citations of This Product
Riferimenti
1. Ma Liang, Zhu Yindi, Chen Xueming, Fang Raohao, Chen Yuru, Xu Xia, Huang Guozheng, Liu Zi, Liu Xiang.  (2021)  A novel nickel-modified nano-magnetite for isolation of histidine-tagged proteins expressed in Escherichia coli.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  413  (27): (6813-6821).  [PMID:34491395] [10.1007/s00216-021-03637-5]
2. Fengfeng Dong, Qishen Huang, Shufeng Pang, Yun-Hong Zhang.  (2024)  Hydrogel network formation triggers atypical hygroscopic behavior in atmospheric aerosols.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:39488286] [10.1016/j.scitotenv.2024.177298]
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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.