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Merck
CN

454680

(R)-(−)-Glycidyl methyl ether

97%

Synonym(s):

(R)-(−)-2-(Methoxymethyl)oxirane, (R)-(−)-Methyl glycidyl ether

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About This Item

Empirical Formula (Hill Notation):
C4H8O2
CAS Number:
64491-70-9
Molecular Weight:
88.11
Beilstein:
102505
MDL number:
MFCD00273372
UNSPSC Code:
12352005
PubChem Substance ID:
24868954
NACRES:
NA.22

Key Documents

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Quality Level

100

Assay

97%

optical activity

[α]20/D −15°, c = 5 in toluene

refractive index

n20/D 1.406 (lit.)

bp

110-111 °C (lit.)

density

0.982 g/mL at 25 °C (lit.)

functional group

ether

SMILES string

COC[C@H]1CO1

InChI

1S/C4H8O2/c1-5-2-4-3-6-4/h4H,2-3H2,1H3/t4-/m0/s1

InChI key

LKMJVFRMDSNFRT-BYPYZUCNSA-N

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Related Categories

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

EUH019

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

62.6 °F - closed cup

Flash Point(C)

17 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS5716
MKCS4434
MKCM9657
MKBR8834V
MKBQ7962V

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Young-Gyun Park et al.
Nature biotechnology (2018-12-18)
Understanding complex biological systems requires the system-wide characterization of both molecular and cellular features. Existing methods for spatial mapping of biomolecules in intact tissues suffer from information loss caused by degradation and tissue damage. We report a tissue transformation strategy

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