CAS 51594-55-9|(R)-(-)-Epichlorohydrin
| Common Name | (R)-(-)-Epichlorohydrin | ||
|---|---|---|---|
| CAS Number | 51594-55-9 | Molecular Weight | 92.524 |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 116.1±0.0 °C at 760 mmHg |
| Molecular Formula | C3H5ClO | Melting Point | -48ºC |
| MSDS | Chinese | Flash Point | 33.9±0.0 °C |
| Symbol | GHS02, GHS05, GHS06, GHS08 | Signal Word | Danger |
Names
| Name | (R)-epichlorohydrin |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 116.1±0.0 °C at 760 mmHg |
| Melting Point | -48ºC |
| Molecular Formula | C3H5ClO |
| Molecular Weight | 92.524 |
| Flash Point | 33.9±0.0 °C |
| Exact Mass | 92.002892 |
| PSA | 12.53000 |
| LogP | 0.45 |
| Vapour Pressure | 22.0±0.2 mmHg at 25°C |
| Index of Refraction | 1.444 |
| InChIKey | BRLQWZUYTZBJKN-VKHMYHEASA-N |
| SMILES | ClCC1CO1 |
| Storage condition | 2~8°C |
Toxicological Information
CHEMICAL IDENTIFICATION |
ACUTE TOXICITY DATA - TYPE OF TEST :
- Mutation test systems - not otherwise specified
- TYPE OF TEST :
- Cytogenetic analysis
MUTATION DATA - TEST SYSTEM :
- Rodent - mouse
- DOSE/DURATION :
- 100 mg/kg
- REFERENCE :
- MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 298,197,1993
- TEST SYSTEM :
- Rodent - mouse
- DOSE/DURATION :
- 100 mg/kg
- REFERENCE :
- MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 298,197,1993
Safety Information
| Symbol | GHS02, GHS05, GHS06, GHS08 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H226-H301-H311-H314-H317-H331-H350 |
| Precautionary Statements | P201-P261-P280-P301 + P310-P305 + P351 + P338-P310 |
| Personal Protective Equipment | Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Hazard Codes | T:Toxic |
| Risk Phrases | R10;R23/24/25;R34;R43;R45 |
| Safety Phrases | S45-S53 |
| RIDADR | UN 2023 |
| WGK Germany | 3 |
| RTECS | RR0427000 |
| Packaging Group | II |
| Hazard Class | 6.1 |
| HS Code | 2910900090 |
Customs
| HS Code | 2910900090 |
|---|---|
| Summary | 2910900090. epoxides, epoxyalcohols, epoxyphenols and epoxyethers, with a three-membered ring, and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Articles4
More Articles| Halogenated derivatives QSAR model using spectral moments to predict haloacetic acids (HAA) mutagenicity. Bioorg. Med. Chem. 16 , 5720-32, (2008) The risk of the presence of haloacetic acids in drinking water as chlorination by-products and the shortage of experimental mutagenicity data for most of them requires a research work. This paper desc... | |
| The intramolecular asymmetric Pauson-Khand cyclization as a novel and general stereoselective route to benzindene prostacyclins: synthesis of UT-15 (treprostinil). J. Org. Chem. 69 , 1890, (2004) A general and novel solution to the synthesis of biologically important stable analogues of prostacyclin PGI(2), namely benzindene prostacyclins, has been achieved via the stereoselective intramolecul... | |
| Strategy for the enantioselective synthesis of trans-2,4-disubstituted piperidines: application to the CCR3 antagonist IS811. J. Org. Chem. 71 , 8975, (2006) A strategy for the enantioselective synthesis of trans-2,4-disubstituted piperidines is proposed and applied to the preparation of IS811, a potent CCR3 antagonist. The C2 stereocenter is derived from ... |
Synonyms
| EINECS 424-280-2 |
| (2R)-(Chloromethyl)oxirane |
| (R)-Chloromethyloxirane |
| EPICHLOROHYDRIN, (-)- |
| (R)-3-Chloropropylene Oxide |
| (2R)-(-)-2-(Chloromethyl)oxirane |
| (2R)-(-)-3-Chloro-1,2-propenoxide |
| (R)-(-)-Epichlorohydrin |
| (R)-(−)-Epichlorohydrin |
| (-)-Epichlorohydrin |
| MFCD00077759 |
| (R)-Epichlorohydrin |
| ()-Chloromethyl oxirane |
| (2R)-2-(Chloromethyl)oxirane |
| Oxirane, 2-(chloromethyl)-, (2R)- |
| (-)-2-(Chloromethyl)oxirane |
| T3OTJ B1G &&(R)-(-)- Form |
| (R)-1-Chloro-2,3-epoxypropane |
