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OEM Customized Methyl (S)-(-)-2-Chloropropionate - D-(+)-Camphoric Acid CAS 124-83-4 Purity 99.0%~101.0% High Purity – Ruifu Featured Image
  • OEM Customized Methyl (S)-(-)-2-Chloropropionate - D-(+)-Camphoric Acid CAS 124-83-4 Purity 99.0%~101.0% High Purity – Ruifu

OEM Customized Methyl (S)-(-)-2-Chloropropionate - D-(+)-Camphoric Acid CAS 124-83-4 Purity 99.0%~101.0% High Purity – Ruifu

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OEM Customized Methyl (S)-(-)-2-Chloropropionate - D-(+)-Camphoric Acid CAS 124-83-4 Purity 99.0%~101.0% High Purity – Ruifu Detail:

Supply with High Purity and Stable Quality
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Chemical Name D-(+)-Camphoric Acid
Synonyms (+)-Camphoric Acid; (1R,3S)-(+)-Camphoric Acid
CAS Number 124-83-4
CAT Number RF-CC275
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C10H16O4
Molecular Weight 200.23
Density 1.1860
Solubility Solube in Methanol
Shipping Condition Shipped Under Ambient Temperature
Brand Ruifu Chemical
Item Specifications
Appearance White Crystalline Powder
Purity 99.0%~101.0%
Melting Point 185.0~190.0℃
Specific Rotation [α]D20 ≥+45.0°
Loss On Drying ≤0.50%
Heavy Metals (Pb) ≤20ppm
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates; Chiral Compounds

Package: Bottle, Aluminium foil bag, Cardboard Drum, 25kg/Drum, or according to customer’s requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

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Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of D-(+)-Camphoric Acid (CAS: 124-83-4) with high quality, widely used in organic synthesis, synthesis of pharmaceutical intermediates and Active Pharmaceutical Ingredient (API) synthesis.

D-(+)-Camphoric Acid (CAS: 124-83-4) is used primarily as a reagent in syntheses of crystalline structures. It is used in the preparation of polymeric transition metal dipyridylamine D-camphorate complexes. D-(+)-Camphoric Acid (CAS: 124-83-4) may be used in the preparation (1R,2S,3R,5S)-2,3-dibenzyl-1,8,8-trimethyl-3-thianiumbicyclo[3.2.1]octane perchlorate. It reacts with uranyl nitrate in pyridine(py) or py/methanol(MeOH) to form novel uranyl-organic assemblages.

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