6-Chlorohexanol

6-Chlorohexanol Basic information
Product Name:6-Chlorohexanol
Synonyms:6-chloro-1-hexano;omega-chlorohexanol;6-CHLOROHEXYL CYANIDE 97%;1-CHLORO-6-HYDROXYHEXANE, 6-CHLORO-1-HEXANOL;1-Chloro-6-hydroxyhexane, Hexamethylene chlorohydrin;6-Chloro-1-hexanol ,95%;1-Chloro-6-hydroxyhexane,95%;6-Chlorohexan-1-ol 97+%
CAS:2009-83-8
MF:C6H13ClO
MW:136.62
EINECS:217-925-2
Product Categories:Pharmaceutical Intermediates;omega-Chloroalkanols;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;OLED materials,pharm chemical,electronic;API Intermediate
Mol File:2009-83-8.mol
6-Chlorohexanol Structure
6-Chlorohexanol Chemical Properties
Melting point 102 °C
Boiling point 108-112 °C14 mm Hg(lit.)
density 1.024 g/mL at 25 °C(lit.)
vapor pressure 1.066hPa at 21.1℃
refractive index n20/D 1.456(lit.)
Fp 210 °F
storage temp. Sealed in dry,Room Temperature
solubility Soluble in dimethylformamide.
form Liquid
pka15.17±0.10(Predicted)
Specific Gravity1.024
color Clear colorless to pale yellow
Water Solubility 11.3g/L at 20℃
BRN 1697307
InChIKeyJNTPTNNCGDAGEJ-UHFFFAOYSA-N
LogP1.86 at 30℃
CAS DataBase Reference2009-83-8(CAS DataBase Reference)
NIST Chemistry Reference1-Hexanol, 6-chloro-(2009-83-8)
EPA Substance Registry System1-Hexanol, 6-chloro- (2009-83-8)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21-36/38-36/37/38-20/21/22
Safety Statements 26-36/37-36/37/39
RIDADR 2810
WGK Germany 3
RTECS MO9160000
TSCA T
HazardClass IRRITANT
HS Code 29055900
Toxicitymouse,LD50,intraperitoneal,> 100mg/kg (100mg/kg),Journal of Organic Chemistry. Vol. 21, Pg. 739, 1956.
MSDS Information
ProviderLanguage
1-Chloro-6-hydroxyhexane English
SigmaAldrich English
ACROS English
ALFA English
6-Chlorohexanol Usage And Synthesis
Chemical Propertiesclear colorless to pale yellow liquid
Uses6-Chloro-1-hexanol is used in the preparation of its corresponding bromide by reaction with sodium bromide using N,N-dimethylformamide and dibromomethane (2:1) as a solvent. It is utilized in the selective elimination of 6-chloro-1-hexene from esters of 6-chloro-1-hexanol.
Preparation6-Chlorohexanol is obtained from the reaction of 1,6-Hexanediol with hydrochloric acid.
Synthesis Reference(s)Organic Syntheses, Coll. Vol. 3, p. 446, 1955
Tetrahedron Letters, 36, p. 3161, 1995 DOI: 10.1016/0040-4039(95)00501-3
Epichlorohydrin rubber 1-CHLORO-4-HYDROXYCYCLOHEXANE N,3,4,6-O-Tetraacetyl-α-D-galactosaMinyl Chloride 3,3-DICHLORO-2,2-DIHYDROXYCYCLOHEXANONE 2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL CHLORIDE 3,4,6-TRIACETATE 2-CHLOROCYCLOHEXANOL 6-CHLORO-N-HEXANOIC ACID (+)-CAMPHANIC ACID CHLORIDE 6-CHLOROHEXANOL [489.1.8 MOR] 6-CHLORO-6-DEOXY-ALPHA-D-GLUCOPYRANOSE Clobetasol propionate 4-chloro-2-hexanol Diallyl 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate 6-CHLORO-6-DEOXY-D-MANNOSE 2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL CHLORIDE Chlorhexidine diacetate 6-CHLORO-6-DEOXY-ALPHA-D-MANNOSE 2,2,6,6-TETRACHLOROCYCLOHEXANOL

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