(1S,2S)-(-)-1,2-Diphenylethylenediamine | CAS 29841-69-8

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Name (1S,2S)-(−)-1,2-Diphenylethylenediamine; (1S,2S)-(−)-1,2-Diamino-1,2-diphenylethane
CAS 29841-69-8
Appearance White crystal powder
Molecular Formula C14H16N2
Molecular Weight 212.29
Assay 98%
Packing; Delivery 100g, 1kg, 25Kg/drum; Delivery within 3-5 working days
Sample Available
Payment L/C, D/A, D/P, T/T, Other

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  • We provide free samples, trial orders, bulk purchases of tons of (1S,2S)-(-)-1,2-Diphenylethylenediamine, procurement tiered pricing, and cost reduction 15%+.
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(1S,2S)-(-)-1,2-Diphenylethylenediamine Basic Information, Physicochemical Properties, etc.

Basic Information
Name (1S,2S)-(-)-1,2-Diphenylethylenediamine
Synonyms (1S,2S)-(-)-1,2-Diphenyl-1,2-ethanediamine,99%,ee:99%;(1S,2S)-(-)-1,2-Diphenylethylenediamine,99%;(1S,2S)-(-)-1,2-Diph;1S,2S-diphenylethane-1,2-diamine;(1S,2S)-(-)Chemicalbook-1,2-Diphenyl-1,2-ethanediamineee;(1S,2S)-(-)-1,2-Diphenyl-1,2-ethanediamine,99%,99%ee;((1S,2S)-2-AMino-1,2-diphenylethyl)aMine;(S,S)-1,2-DiaMino-1,2-diphenylethane
CAS Number 29841-69-8
Molecular Formula C14H16N2
Molecular Weight 212.29
EINECS Number 608-420-1
Structural Formula
Physicochemical Properties
Melting Point 83-85 °C(lit.)
Boiling Point 342.14°C (rough estimate)
Density 1.0799 (rough estimate)
Optical Activity [α]20/D 102°, c = 1 in ethanol
Refractive Index -103 ° (C=1, EtOH)
Solubility DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
Water Solubility
Insoluble in water
Form Crystal
Color White to pale yellow
Appearance Colorless needle-shaped crystals are odorless, insoluble in water, easily soluble in methanol and ethanol, and easily oxidized in the air.
Acidity Coefficient (pKa) 9.78±0.10(Predicted)
Safety and Regulatory Information
InChIKey
PONXTPCRRASWKW-KBPBESRZSA-N
BRN 3201645
NIST Chemical Substance Information /
EPA Chemical Substance Information /
Other Information
Detection Methods HPLC

(1S,2S)-(-)-1,2-Diphenylethylenediamine Application, Use, Usage, Synthesis Method, etc.

1. (1S,2S)-1,2-Diphenylethylenediamine is a compound that can be used in organic synthesis.

2. Widely used in asymmetric synthesis and optical resolution:

  • Asymmetric hydroxylation of olefins
  • Asymmetric aldol condensation
  • Asymmetric Diels-Alder reaction
  • Asymmetric allylation of carbonyl
  • Synthesis of optically active allenyl alcohols and propargyl alcohols
  • Asymmetric epoxidation of olefins without functional groups
  • Resolution of binaphthol

Preparation

The current preparation method is to treat (±)-1,2-diphenylethylenediamine in ethanol solvent with tartaric acid as a resolution agent, and adopt different resolution conditions according to the needs to obtain (1S,2S)-1,2-diphenylethylenediamine or (1R,2R)-1,2-diphenylethylenediamine.

(1S,2S)-(−)-1,2-Diamino-1,2-diphenylethane Packaging, Storage, Delivery, Transportation, etc.

Packing: 100g 1kg drum 25Kg/drum

Storage: Nitrogen protection, air sensitive, keep in dark place, sealed in dry, room temperature

Delivery: delivery within 3- 5 working days

Transportation: According to your needs

FAQ About (1S,2S)-(−)-1,2-Diamino-1,2-diphenylethane

1. What is (1S,2S)-(−)-1,2-Diamino-1,2-diphenylethane?

Answer: It is a chiral molecule with the appearance of white to light yellow crystalline powder and is an important pharmaceutical intermediate.

2. What solvents are suitable for dissolving this compound?

Answer:

  • Polar aprotic solvents: Dichloromethane, chloroform.
  • Alcohols: DMSO, Methanol, ethanol (partial solubility).
  • Avoid water due to limited solubility.

3. What distinguishes (1S,2S)-(−)-1,2-Diamino-1,2-diphenylethane from its enantiomer (1R,2R)-(+)-form?

Answer:

  • Stereochemistry: The (1S,2S) configuration is the mirror image of (1R,2R).
  • Optical rotation: The (−)-form rotates plane-polarized light to the left, while the (+)-form rotates it to the right.
  • Applications: Opposite enantiomers may show different catalytic or biological activities.

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