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CAS: 26530-20-1
MF: C11H19NOS
MW: 213.34
EINECS: 247-761-7
Description
Parmetol N 20, octylisothiazolinone, is contained in relatively fewer products than other isothiazolinones.
Parmetol N 20 a member of the class of 1,2-thiazole that is 1,2-thiazol-3-one substituted on the nitrogen (position 2) by an octyl group.
A fungicide and antibacterial agent, Parmetol N 20 is used for treatment of canker and other fungal and bacterial diseases in fruit trees.
Parmetol N 20 no longer approved for use within the European Union.
Parmetol N 20 is clear dark amber liquid.
Parmetol N 20 used as a fungicide.
Parmetol N 20 Chemical Properties
Melting point: <25 °C
Boiling point: 120°C
Density: 1.04
Vapor pressure: 4.9hPa at 25℃
Refractive index: 1.5500 (estimate)
Fp: 23℃
Storage temp.: Sealed in dry,2-8°C
pka: -2.04±0.20(Predicted)
Form: neat
Color: White or Colorless to Yellow
Water Solubility: <0.1 g/100 mL at 19 ºC
Merck: 14,6755
BRN: 1211137
Stability: Stable. Incompatible with strong oxidizing agents.
InChIKey: JPMIIZHYYWMHDT-UHFFFAOYSA-N
LogP: 2.61 at 25℃
CAS DataBase Reference: 26530-20-1(CAS DataBase Reference)
NIST Chemistry Reference: 3(2H)-isothiazolone, 2-octyl-(26530-20-1)
EPA Substance Registry System: Octhilinone (26530-20-1)
Yellow solid or clear dark amber liquid.
Uses
Parmetol N 20 use to fungicide.
Biocide in cooling-tower water, paints, cutting oils, cosmetics and shampoo; for leather preservation.
Parmetol N 20 is a mildeweide; bactericide; fungicide; biocide in cooling-tower water; in paints, cutting oils, cosmetics, and shampoos; leather preservation; wound protectant for pruning cuts.
Incompatibilities
Parmetol N 20 is oxidizers.
Contact with hydrogen peroxide may form explosive material.
Parmetol N 20 are incompatible with many classes of compounds, reacting exothermically to release toxic gases.
Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat.
Ketones behave a weak acid.
Forms water soluble alkali metal salts.
Ketones are reactive with many acids and bases liberating heat and flammable gases.
The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone.
Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable hydrogen gas and heat.
Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides.
They react violently with aldehydes, nitric acid, and perchloric acid.
Synonyms
Octhilinone
26530-20-1
2-octylisothiazol-3(2H)-one
2-n-Octyl-4-isothiazolin-3-one
2-Octyl-4-isothiazolin-3-one
2-Octyl-3-isothiazolone
Pancil
2-Octyl-2H-isothiazol-3-one
3(2H)-Isothiazolone, 2-octyl-
Kathon 893
2-Octyl-3(2H)-isothiazolone
Skane 8
Skane M-8
Kathon 893F
Micro-chek skane
Kathon LM
Microbicide M-8
2-octyl-1,2-thiazol-3-one
Micro-chek 11
Micro-chek 11D
Kathon SP 70
Kathon LP preservative
Kathon 4200
4-Isothiazolin-3-one, 2-octyl-
Octyl-3(2H)-isothiazolone
2-Octyl-3-isothioazolone
2-Octyl-3-isothiazolinone
Octyl-4-isothiazol-3-one
2-n-Octyl-3-isothiazolone
4LFS24GD0
MLS002415697
CHEBI:81936
SMR001370885
DSSTox_CID_5805
Pancil-T
DSSTox_RID_77928
DSSTox_GSID_25805
Skane M8
Caswell No. 613C
Kathon
Vinylzene IT 3000DIDP
RH 893
CAS-26530-20-1
Octhilinone [ANSI:BSI:ISO]
CCRIS 6082
EINECS 247-761-7
UNII-4LFS24GD0V
EPA Pesticide Chemical Code 099901
BRN 1211137
Pancil T
2-octyl-1,2-thiazol-3(2H)-one
Skane M 8
Vinyzene IT 3000DIDP
SCHEMBL15648
cid_33528
SCHEMBL396433
CHEMBL1562104
DTXSID1025805
BDBM66023
HSDB 6713
2-Octyl-4-Isothiazolin-3-Ketone
ZINC2012904
Tox21_201459
Tox21_300566
MFCD00072473
RH-893
AKOS015897428
NCGC00091875-01
NCGC00091875-02
NCGC00091875-03
NCGC00091875-04
NCGC00091875-05
NCGC00254466-01
NCGC00259010-01
AS-11894
Octhilinone 10 microg/mL in Acetonitrile
DB-028182
FT-0613248
O0343
O0378
C18752
D91863
530O201
Q2013949
W-107168
2-Octyl-4-isothiazolin-3-one, PESTANAL(R), analytical standard
