D-Threitol - ≥99% , CAS No.2418-52-2

CAS: 2418-52-2 Cat. No.: S197225 Fórmula: HOCH2[CH(OH)]2CH2OH Peso molecular: 122.12 Beilstein Registry Number: 1719752 Número EC: 621-282-7
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
DL-Threitol, 97% | 1,2,3,4-Butanetetrol, (R*,R*)- | 3VB | DTXSID801016717 | 082CB5C6-FE44-4BE0-BEE0-8575D840C94A | F85623 | UNII-6DN82XBT5M | (R*,R*)-1,2,3,4-Butanetetrol | Threitol, D- | (2R,3R)-1,2,3,4-Butanetetrol | D-Threitol, 99% | rel-(2R,3R)-butane
Storage
Room temperature
Shipped In
Normal
★
Size
Alemania (EU)
USA*
Price
Qty
250mg
S197225-250mg
Fabricado bajo pedido · 8–12 semanas
357,42€
1g
S197225-1g
Fabricado bajo pedido · 8–12 semanas

1.022,11€

1.192,19€
Guardar 170,08 € (14.27%)
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Why this grade

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

🌡

Storage & shipping

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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

D-Threitol is a chiral tetrol used in the preparation of chiral bis-crown ethers. Also used in the synthesis of the threo-L-tetramine via a tetrasulfonate.

Specifications

Sinónimos
DL-Threitol, 97% | 1,2,3,4-Butanetetrol, (R*,R*)- | 3VB | DTXSID801016717 | 082CB5C6-FE44-4BE0-BEE0-8575D840C94A | F85623 | UNII-6DN82XBT5M | (R*,R*)-1,2,3,4-Butanetetrol | Threitol, D- | (2R,3R)-1,2,3,4-Butanetetrol | D-Threitol, 99% | rel-(2R,3R)-butane
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥99%
Nombres e identificadores
Sonrisas canónicasC(C(C(CO)O)O)O
IUPAC Name(2R,3R)-butane-1,2,3,4-tetrol
InChIKeyUNXHWFMMPAWVPI-QWWZWVQMSA-N
INCHI1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2/t3-,4-/m1/s1
Isómeros SMILES C([C@H]([C@@H](CO)O)O)O
Peso molecular 122.12
Beilstein 1719752
Reaxy-Rn 1735878
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1735878&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 ParentSugar alcohols
Alternative Parents Secondary alcohols  Polyols  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Sugar alcohol - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
External Descriptors threitol
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:
Propiedades químicas y físicas
SolubilidadSoluble in water. Insoluble in ethyl ether, and benzene., Soluble in water. Insoluble in ethyl ether, and benzene.
Peso molecular122.120 g/mol
XLogP3-2.300
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass122.058 Da
Monoisotopic Mass122.058 Da
Topological Polar Surface Area80.900 Ų
Heavy Atom Count8
Formal Charge0
Complexity48.000
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
Referencias
1. Yingshuang Hui, Yulu Zhan, Wenrong Hou, Lou Gao, Yahong Zhang, Yi Tang.  (2021)  Product Control and Insight into Conversion of C6 Aldose Toward C2, C4 and C6 Alditols in One-Pot Retro-Aldol Condensation and Hydrogenation Processes.  ChemistryOpen,  10  (5): (560-566).  [PMID:33945238] [10.1002/open.202100023]
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