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 3-Chloroacetophenone

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3-Chloroacetophenone Molecular Weight: 154.593580 [g/mol]
 

 

 

 

 

 

 

 

 
















 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


 

HOME >> Chemicals >> 3-Chloroacetophenone


 3-Chloroacetophenone logo
 

 3-Chloroacetophenone

 3-Chloroacetophenone structure
 

IUPAC Name: 1-(3-chlorophenyl)ethanone

Synonyms:
3'-Chloroacetophenone, omega-Chloroacetophenone,CHLOROACETOPHENONE, Ambap7200, Acetophenone, 3'-chloro-, Ethanone, 1-(3-chlorophenyl)-, 1-(3-Chlorophenyl)ethanone, CCRIS 638, 288799_ALDRICH, 22845_FLUKA, EINECS 202-721-8, ZINC02039606, Ethanone, 1-phenyl-, monochloro deriv, Ethanone, 1-phenyl-, monochloro deriv., LS-67567, InChI=1/C8H7ClO/c1-6(10)7-3-2-4-8(9)5-7/h2-5H,1H, 99-02-5, 1341-24-8, 29731-15-5

CAS Registry Number: 99-02-5
Molecular Formula: C8H7ClO
Molecular Weight: 154.593580 [g/mol]
Density 1.184
Boiling point 241 șC
Flash point 105 șC

Other chemicals were found as well: chlorodiphenyl (which can cause liver damage and irritate the eyes and skin), chloroacetophenone (tear gas), phosgene (a colorless gas that can cause weakness lasting weeks or months), hydrogen cyanide (a colorless gas with a slight almond-like odor that at low-level exposures can cause breathing difficulties, heart pains, vomiting, and headache), and trichloroarsine (which affects respiration and can cause cancer).

Phenacyl chloride is a substituted acetophenone. It is a useful building block in organic chemistry. Apart from that, it has been historically used as a riot control agent, where it is designated CN.

Preparation
Phenacyl chloride is readily available commercially. It may be synthesized by the Friedel-Crafts acylation of benzene using chloroacetyl chloride, with an aluminium chloride catalyst

 Uses
* 3-Chloroacetophenone is primarily used as a riot-control agent (tear gas) and in Chemical Mace. (1-3,7)
* It is also used as a pharmaceutical intermediate and formerly as an alcohol denaturant.

Sources and Potential Exposure
* The use of tear gas and Chemical Mace to control riots and disable attackers causes direct exposure to 3-Chloroacetophenone through skin contact and inhalation.

Occupational exposure may occur during its manufacture and use by inhalation and dermal contact.

Assessing Personal Exposure

* No information was located regarding the measurement of personal exposure to 3-Chloroacetophenone.

Health Hazard Information
Acute Effects:
* 3-Chloroacetophenone is a potent eye, throat, and skin irritant. Acute inhalation exposure of humans causes burning of the eyes with lacrimation; some degree of blurred vision; possible corneal damage; irritation and burning of the nose, throat, and skin; burning in the chest with dyspnea; and laryngotracheobronchitis

Acute dermal exposure is irritating and can result in first, second, and third degree chemical burns in humans; these effects are exacerbated when the skin is wet. Acute animal tests in rats, mice, rabbits, and guinea pigs have demonstrated 3-Chloroacetophenone to have high acute toxicity from oral exposure.

Preparation

Note: These API/ chemicals are designated as those that are used in the manufacture of the controlled substances and are important to the manufacture of the substances. For any (Control Substance) products Import and Export *** subjected to your country government laws /control substance ACT.

Note /Government Notification:  N/A

 
               
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 3-Chloroacetophenone 3-Chloroacetophenone CAS Registry Number: 99-02-5
3-Chloroacetophenone Molecular Formula: C8H7ClO


 


 


 


 

 

 

 

 

 

 

 

 

 

 


 

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