(R)-(-)-Epichlorohydrin

Base Information Edit

Chemical Name:(R)-(-)-Epichlorohydrin
CAS No.:51594-55-9
Molecular Formula:C3H5ClO
Molecular Weight:92.5251
Hs Code.:29103000
European Community (EC) Number:424-280-2,628-656-9
UNII:VEC01H609I
DSSTox Substance ID:DTXSID501014417
Nikkaji Number:J112.276B
Wikidata:Q26840862
Metabolomics Workbench ID:53645
ChEMBL ID:CHEMBL448626
Mol file:51594-55-9.mol

Synonyms:(R)-(-)-Epichlorohydrin;51594-55-9;(R)-Epichlorohydrin;(2R)-2-(chloromethyl)oxirane;r-epichlorohydrin;(-)-Epichlorohydrin;(R)-(Chloromethyl)oxirane;(R)-2-(Chloromethyl)Oxirane;Epichlorohydrin, (-)-;R-(-)-Epichlorohydrin;Oxirane, (chloromethyl)-, (2R)-;(R)-1-Chloro-2,3-epoxypropane;(R)-3-chloro-1,2-epoxypropane;Oxirane, (chloromethyl)-, (R)-;UNII-VEC01H609I;CCRIS 6387;VEC01H609I;CHEBI:18662;BRN 1420785;EC 424-280-2;(R)-(-)-Epichlorohydrin, 99%;2-(Chloromethyl)oxirane #;5-17-01-00020 (Beilstein Handbook Reference);r-epichlorohydrine;R-epi-chlorohydrin;(R)-(-)-2-(Chloromethyl)oxirane;(r)-epichlorohydrine;(r)-(-)-1-chloro-2,3-epoxypropane;(R)-epi-chlorohydrin;R-(-)-epichlorhydrin;(R)(-)epichlorohydrin;R-(-) epichlorohydrin;(R)-Chloromethyloxirane;(R)-(-)Epichlorhydrin;(r)-(-)epichlorohydrin;(R)-(-)epichlorhydrine;(R)-Chloromethyl oxirane;(r)-(-)-epiclorohydrin;(r)-(+)-epichlorohydrin;(R)-(-)-epichlorhydrine;(r)-(-)-epichlorohydrine;(R)-2-chloromethyl-oxirane;(R)-3-Chloropropylene Oxide;R-1-cloro-2,3-epoxipropano;(R)-2-(chloromethyl) oxirane;(R,S)-2-Chloromethyl-oxirane;CHEMBL448626;(R)-1-Cloro-2,3-Epossipropano;DTXSID501014417;BCP08874;STR07309;MFCD00077759;AKOS006240274;AKOS015848754;R-1-CHLORO-2,3-EPOXYPROPANE;AC-7036;CS-O-31249;Oxirane, 2-(chloromethyl)-, (2R)-;AM20090812;CS-0005957;E0581;EN300-54611;A828677;J-524218;Q26840862

Suppliers and Price of (R)-(-)-Epichlorohydrin

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(R)-Epichlorohydrin
10g
$ 145.00

TRC
(R)-Epichlorohydrin
5g
$ 95.00

TCI Chemical
(R)-Epichlorohydrin >98.0%(GC)
5g
$ 17.00

TCI Chemical
(R)-Epichlorohydrin >98.0%(GC)
25g
$ 45.00

SynQuest Laboratories
(2R)-(-)-3-Chloro-1,2-propenoxide 99%
25 g
$ 45.00

SynQuest Laboratories
(2R)-(-)-3-Chloro-1,2-propenoxide 99%
500 g
$ 221.00

SynQuest Laboratories
(2R)-(-)-3-Chloro-1,2-propenoxide 99%
100 g
$ 80.00

Sigma-Aldrich
(R)-(?)-Epichlorohydrin 99%
5g
$ 135.00

Sigma-Aldrich
(R)-(?)-Epichlorohydrin 99%
25g
$ 53.00

Oakwood
R-(-)-Epichlorohydrin
1g
$ 10.00

Total 170 raw suppliers

Chemical Property of (R)-(-)-Epichlorohydrin Edit

Chemical Property:

Appearance/Colour:colorless to light yellow liquid
Vapor Pressure:10 mm Hg ( 16.6 °C)
Melting Point:-48ºC
Refractive Index:n20/D 1.438(lit.)
Boiling Point:116.1 ºC at 760 mmHg
Flash Point:33.9 ºC
PSA：12.53000
Density:1.183 g/cm³
LogP:0.62400
Storage Temp.:2-8°C
Water Solubility.:insoluble
XLogP3:0.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:92.0028925
Heavy Atom Count:5
Complexity:37.9

Purity/Quality:

99% ^*data from raw suppliers

(R)-Epichlorohydrin ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 45-10-23/24/25-34-43
Safety Statements: 53-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(O1)CCl
Isomeric SMILES:C1[C@@H](O1)CCl
Uses ((R)-Epichlorohydrin) R-enantiomer of Epichlorohydrin, an important industrial chemical, is a bifunctional alkylating agent with the potential to form DNA cross-links. It is used as a solvent for natural and synthetic resins, gums, cellulose esters and ethers, paints, varnishes, nail enamels and lacquers, cement for Celluloid. Also, it is used as stabilizer. Building block for the synthesis of a key intermediate in the synthesis of stable PGI2 analogue UT-15.

Technology Process of (R)-(-)-Epichlorohydrin

There total 24 articles about (R)-(-)-Epichlorohydrin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%