Ethyl 4-Chloro-3-Hydroxybutanoate CAS 10488-69-4 Assay ≥98.0% (GC) High Purity
Manufacturer Supply with High Purity and Stable Quality
Ethyl 4-Chloro-3-Hydroxybutanoate CAS 10488-69-4
Ethyl (S)-4-Chloro-3-Hydroxybutyrate CAS 86728-85-0
Ethyl (R)-(+)-4-Chloro-3-Hydroxybutyrate CAS 90866-33-4
Chiral Compounds, High Quality, Commercial Production
Chemical Name | Ethyl 4-Chloro-3-Hydroxybutanoate |
Synonyms | DL-Ethyl 4-Chloro-3-Hydroxybutyrate |
CAS Number | 10488-69-4 |
CAT Number | RF-CC187 |
Stock Status | In Stock, Production Scale Up to Tons |
Molecular Formula | C6H11ClO3 |
Molecular Weight | 166.6 |
Melting Point | 136℃ |
Brand | Ruifu Chemical |
Item | Specifications |
Appearance | Colorless to Pale Yellow Liquid |
Assay / Analysis Method | ≥98.0% (GC) |
Ethyl 4-Chloroacetoacetate | ≤0.30% |
Moisture (K.F) | ≤0.30% |
Dichloromethane | ≤0.50% |
Ethanol | ≤1.50% |
pH | 5.0~7.0 |
Test Standard | Enterprise Standard |
Usage | Pharmaceutical Intermediate |
Package: Bottle, Aluminum 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.


Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Ethyl 4-Chloro-3-Hydroxybutanoate (CAS: 10488-69-4) with high quality, widely used in organic synthesis, synthesis of pharmaceutical intermediates and Active Pharmaceutical Ingredient (API) synthesis.
Ethyl 4-Chloro-3-Hydroxybutanoate (CAS: 10488-69-4) is a key chiral intermediate in statins. It is an intermediate of Olacetam, Olacetam in the treatment of alzheimer's disease. Ethyl 4-Chloro-3-Hydroxybutanoate (CAS: 10488-69-4), it is an important organic intermediate to synthesize precursor compounds of cholesterol-lowering drugs, but also for many activities synthesis of drugs such as hydroxymethylglutaryl reductase inhibitors and 1,4-dihydropyridine β-blockers. It has the advantage of being easy to synthesize and inexpensive, and it is a very cost-effective way to prepare Ethyll-4-Chloro-3-Hydroxy Butyrate by asymmetric reduction as a reaction raw material.
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