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(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate, 98%
(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate, 98%
(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate, 98%
Thermo Scientific Chemicals

(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate, 98%

CAS: 39961-95-0 | C10H20N2O6 | 264.278 g/mol
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Catalog number H60172.09
also known as H60172-09
Price (USD)
128.65
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Ends: 30-Jun-2026
151.00
Save 22.35 (15%)
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Quantity:
10 g
Request bulk or custom format
Price (USD)
128.65
Special offer
Online exclusive
Ends: 30-Jun-2026
151.00
Save 22.35 (15%)
Each
Chemical Identifiers
CAS39961-95-0
IUPAC Name2,3-dihydroxybutanedioic acid; cyclohexane-1,2-diamine
Molecular FormulaC10H20N2O6
InChI KeyGDOTUTAQOJUZOF-UHFFFAOYNA-N
SMILESNC1CCCCC1N.OC(C(O)C(O)=O)C(O)=O
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SpecificationsSpecification SheetSpecification Sheet
Assay (unspecified)>97.5%
(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate is a useful chemical for the synthesis of chiral ligands.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate is a useful chemical for the synthesis of chiral ligands.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Daniel Garcia Velazquez; David Diaz; Angel Gutierrez Ravelo; Jose Juan Marrero Tellado. Instantaneous low temperature gelation by a multicomponent organogelator liquid system based on ammonium salts. J. Am. Chem. Soc. 2008, 130,(25), 7967-7973.
  2. Rafal Kowalczyk; Jacek Skarzewski. Asymmetric nitroaldol reaction catalyzed by copper-diamine complexes: selective construction of two contiguous stereogenic centers. Tetrahedron: Asymmetry. 2009, 20,(21), 2467-2473.