Methyl chloroacetate CAS#96-34-4

  • CAS Number:  301-02-0

  • Chemical Formula:  C18H35NO

  • Synonyms:

  • Appearance: Transparent liquid

  • MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)


Product Details

Methyl chloroacetate CAS#96-34-4

A crystalline solid or a solid dissolved in a liquid. Insoluble in water and denser than water. Contact may slightly irritate skin, eyes and mucous membranes. May be slightly toxic by ingestion. Used to make other chemicals.


Methyl chloroacetate Chemical Properties

Melting point 

-33 °C

Boiling point 

130 °C740 mm Hg(lit.)

density 

1.238 g/mL at 25 °C(lit.)

vapor density 

3.8 (vs air)

vapor pressure 

10 mm Hg ( 25 °C)

refractive index 

n20/D 1.422(lit.)

Fp 

125 °F

storage temp. 

Store at <= 20°C.

solubility 

51.6g/l (slow decomposition)

form 

Liquid

color 

Clear colorless

PH

4.6 (28g/l, H2O, 20℃)

explosive limit

4.6-18.5%(V)

Water Solubility 

28 g/L (20 ºC)

Merck 

14,6042

BRN 

506255

Dielectric constant

12.9(20℃)

InChI

1S/C3H5ClO2/c1-6-3(5)2-4/h2H2,1H3

InChIKey

QABLOFMHHSOFRJ-UHFFFAOYSA-N

SMILES

ClCC(=O)OC

LogP

0.63 at 20℃

CAS DataBase Reference

96-34-4(CAS DataBase Reference)

NIST Chemistry Reference

Acetic acid, chloro-, methyl ester(96-34-4)

EPA Substance Registry System

Acetic acid, 2-chloro-, methyl ester (96-34-4)


Safety Information

Hazard Codes 

T,Xi,F

Risk Statements 

10-23/25-37/38-41-40-36/37/38-38

Safety Statements 

26-37/39-45-36-16

RIDADR 

UN 2295 6.1/PG 1

WGK Germany 

2

RTECS 

AF9500000

19

Autoignition Temperature

869 °F

TSCA 

TSCA listed

HS Code 

2915 40 00

HazardClass 

6.1

PackingGroup 

I

Storage Class

3 - Flammable liquids

Hazard Classifications

Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Eye Dam. 1
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3

Hazardous Substances Data

96-34-4(Hazardous Substances Data)

Toxicity

LD50 orally in Rabbit: 107 mg/kg


Product Application Of Methyl chloroacetate CAS#96-34-4

Methyl chloroacetate (MC) is a halogenated ester mainly used as a solvent in organic synthesis or in the preparation of several compounds. Typically, MC is used in the preparation of (carboxymethyl) trimethylammonium chloride estersor in the synthesis of octakis- (carbethoxymethoxy)calix[8]arene. Additionally, methyl chloroacetate acts as an extraction solvent during the separation of neutral compounds with concentration enhancement using coupling liquid–liquid semi-microextraction with micellar electrokinetic chromatography through oncapillary decomposition.

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