C3H5ClO
97.55 g/mol
Research ReagentDanger
Oxirane-d3, (chloromethyl-d2)-
CAS69533-54-6EC685-801-9
Category
Research Reagent
Compound Class
Halocarbon
Primary Use
Research Compound
This compound is a deuterated form of epichlorohydrin, where multiple hydrogen atoms are replaced with deuterium. It is primarily used as a research reagent in laboratories for studies involving isotopic labeling.
research reagent for deuterium labeling studiesinternal standard in analytical chemistry
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 69533-54-6
Related Compounds
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2-chloromethylpyridine hydrochloride
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3-chloromethylpyridine hydrochloride
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research compound
Referencestereoisomer of
Epichlorohydrin
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production of epoxy resins
Referencestereoisomer of
(−)-epichlorohydrin
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pharmaceutical intermediate
Referencestereoisomer of
(+)-epichlorohydrin
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pharmaceutical intermediate
Safety Reference
Danger
H226Flammable liquid and vapour
H301Toxic if swallowed
H311Toxic in contact with skin
H314Causes severe skin burns and eye damage
H317May cause an allergic skin reaction
H331Toxic if inhaled
H350May cause cancer
Identifiers
IUPAC Name
2-[chloro(dideuterio)methyl]-2,3,3-trideuteriooxirane
InChIKey
BRLQWZUYTZBJKN-UXXIZXEISA-N
SMILES
[2H]C1(C(O1)([2H])C([2H])([2H])Cl)[2H]
Synonyms (6)
- (+/-)-Epichlorohydrin-d5