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3,4-Dichlorophenol
Names
Preferred IUPAC name
3,4-Dichlorophenol
Identifiers
3D model ( JSmol)
907693
ChEBI
ChEMBL
ECHA InfoCard 100.002.228 Edit this at Wikidata
EC Number
  • 202-450-5
PubChem CID
UNII
UN number 2020
  • InChI=1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H checkY
    Key: WDNBURPWRNALGP-UHFFFAOYSA-N checkY
  • C1=CC(=C(C=C1O)Cl)Cl
Properties
C6H4Cl2O
Molar mass 163.00 g·mol−1
Odor Phenolic
Melting point 67.8 °C (154.0 °F; 340.9 K) [1]
Boiling point 253 °C (487 °F; 526 K) [1]
Hazards
GHS labelling:
GHS05: Corrosive GHS06: Toxic GHS07: Exclamation mark GHS09: Environmental hazard
Danger
H302, H311, H314, H411
P260, P264, P270, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P361, P363, P391, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond Health 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chloride Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazard COR: Corrosive; strong acid or base. E.g. sulfuric acid, potassium hydroxide
0
1
0
COR
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

3,4-Dichlorophenol (3,4-DCP) is a chlorinated derivative of phenol with the molecular formula Cl2C6H3OH.

References

  1. ^ a b Haynes, p. 3.166

Cited sources

  • Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. ISBN  9781498754293.
Stub icon

This article about an organic halide is a stub. You can help Wikipedia by expanding it.

Retrieved from " https://en.wikipedia.org/?title=3,4-Dichlorophenol&oldid=1162263829"
From Wikipedia, the free encyclopedia
3,4-Dichlorophenol
Names
Preferred IUPAC name
3,4-Dichlorophenol
Identifiers
3D model ( JSmol)
907693
ChEBI
ChEMBL
ECHA InfoCard 100.002.228 Edit this at Wikidata
EC Number
  • 202-450-5
PubChem CID
UNII
UN number 2020
  • InChI=1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H checkY
    Key: WDNBURPWRNALGP-UHFFFAOYSA-N checkY
  • C1=CC(=C(C=C1O)Cl)Cl
Properties
C6H4Cl2O
Molar mass 163.00 g·mol−1
Odor Phenolic
Melting point 67.8 °C (154.0 °F; 340.9 K) [1]
Boiling point 253 °C (487 °F; 526 K) [1]
Hazards
GHS labelling:
GHS05: Corrosive GHS06: Toxic GHS07: Exclamation mark GHS09: Environmental hazard
Danger
H302, H311, H314, H411
P260, P264, P270, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P361, P363, P391, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond Health 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chloride Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazard COR: Corrosive; strong acid or base. E.g. sulfuric acid, potassium hydroxide
0
1
0
COR
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

3,4-Dichlorophenol (3,4-DCP) is a chlorinated derivative of phenol with the molecular formula Cl2C6H3OH.

References

  1. ^ a b Haynes, p. 3.166

Cited sources

  • Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. ISBN  9781498754293.
Stub icon

This article about an organic halide is a stub. You can help Wikipedia by expanding it.

Retrieved from " https://en.wikipedia.org/?title=3,4-Dichlorophenol&oldid=1162263829"

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