ALLYL ISOTHIOCYANATE |
PRODUCT
IDENTIFICATION
|
CAS
NO. |
57-06-7 107231-30-1,
50888-64-7, 50978-48-8, 58391-87-0 (former numbers),
8007-40-7 (Mustard oil) |
|
EINECS
NO. |
200-309-2 |
FORMULA |
CH2=CHCH2NCS |
MOL
WT. |
99.15 |
H.S.
CODE
|
|
TOXICITY |
|
SYNONYMS |
Isothiocyanic
acid, allyl ester; Mustard oil, synthetic; |
3-Isothiocyanato-1-propene;
2-Propenyl
isothiocyanate; Allyl isosulfocyanate; Allyl isosulphocyanate; Allyl mustard oil,
synthetic; Allyl sevenolum; Allylisothiokyanat; Allylsenevol,
Allylsenfoel; Allylsevenolum; Allyspol; Artificial mustard oil;
Artificial oil of mustard; Isothiocyanate d'allyle;
Isothiocyansaeureallylester; Oleum sinapis; |
DERIVATION |
|
CLASSIFICATION
|
|
PHYSICAL
AND CHEMICAL PROPERTIES
|
PHYSICAL
STATE |
Clear
to pale yellow, oily liquid |
MELTING
POINT |
-80
C |
BOILING
POINT |
148
- 153 C |
SPECIFIC
GRAVITY |
1.015
- 1.025 |
SOLUBILITY
IN WATER |
Insoluble |
pH |
|
VAPOR
DENSITY |
|
AUTOIGNITION
|
|
NFPA
RATINGS
|
|
REFRACTIVE
INDEX
|
1.526 - 1.528 |
FLASH
POINT |
46
C |
STABILITY |
Stable
under ordinary conditions. Moisture sensitive |
GENERAL
DESCRIPTION & APPLICATIONS
|
Thiocyanate is a
salt or ester of thiocyanic acid (HSCN). Aqueous solutions of thiocyanic acid ,
also called sulfocyanic acid, are very strong acids of the equilibrium mixture
of thiocyanic and isothiocyanic. Thiocyanates are bonded through the sulfur(s)
with the structure R-S-C¡ÕN or the isomeric R-N=C=S (isothiocyanates).
Thiocyanates are bonded through the sulfur(s) which replace for the oxygen (O)
atom. Thiocyanates are the sulfur analog of isocyanates. Organic as well as
metallic thiocyanates [CuSCN, Ca(SCN)2, NaSCN, KSCN] are
very versatile compounds. They have wide range of applications including
manufacturing industrial chemicals, pharmaceuticals and pesticides. It is used
in freezing solutions, fabric dyeing, electroplating, steel pickling, printing,
and corrosion inhibitor against acid gases. It is used in photography industry
as a stabilizer or accelerator.
Allyl- is the
prefix for the univalent organic group, -CH2=CHCH2. Allyl alcohol is
an example, CH2=CHCH2OH, clear, pungent liquid, boiling at 96 C; soluble in
water. It is prepared from allyl chloride by hydrolysis. Allyl compound,
an alkene hydrocarbon, has a vinyl group, CH2=CH-, attached to a methylene -CH2.
Because of the highly reactive double bond, allyl can undergo free radical addition to double bond which
readily combine with themselves or other monomers to form homopolymers or co-polymers
which are used in the production of coatings, adhesives and elastomers. In addition
to free radical addition,
allyl compounds can participate in a wide variety of reactions
including electrophilic additions, allylic substitution
and oxidation. Allyl,
an unsaturated bond, imparts a characteristic
odor in some compounds. An example is allyl
isothiocyanate which is the main ingredient of black mustards.
(white mustard consists principally of
p-hydroxybenzyl isothiocyanate). Allyl
isothiocyanate is called mustard oil.
Powdered mustard has essentially no aroma until it combines
to moisture. Naturally occurring allyl
isothiocyanate is known to have
anti-tumor and anti-oxidant properties
by inducing the activity
of phase II detoxification enzymes in the urinary bladder. Synthetic allyl
isothiocyanate is used as a fumigant, counterirritant in ointments and plasters
and as
an intermediate to create a desired chemical compound
through a series of chemical reactions, including in the field of fungicide, bactericide, wood preservative,
pharmaceutical and plastic and rubber. |
SALES
SPECIFICATION |
APPEARANCE
|
Clear
to pale yellow, oily liquid |
ASSAY |
98.0%
min |
SPECIFIC
GRAVITY |
1.015
- 1.025 |
REFRACTIVE
INDEX
|
1.526 - 1.528 |
TRANSPORTATION |
PACKING |
200kgs
in drum |
HAZARD
CLASS |
6.1
(Packing Group: II) |
UN
NO. |
1545 |
OTHER
INFORMATION |
Hazard Symbols: T, Risk Phrases: 10-24/25-34-42/43,
Safety Phrases:
23-26-36/37/39-45 FEMA No. 2034 |
|