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Safflower oil ( CASNO:8001-23-8 )

Identification and Related Records
Name:
Safflower oil
CAS Registry number:
8001-23-8
Synonyms:
Carthamustinctorius oil
Diestel oil
Diestelol
Distelol
Fats and Glyceridic oils,safflower
Neobee 18
Oils, glyceridic, safflower
Safflower seed oil
Saffola
Thistle oil
EINECS(EC#):
232-276-5
Molecular Formula:
Unspecified
Molecular Weight:
0
Inchi:
InChI=1S/C4H7ClOS/c1-2-3-7-4(5)6/h2-3H2,1H3
Canonical SMILES:
CCCSC(=O)Cl
Chemical and Physical Properties
Appearance:
yellow liquid
Density:
0.9211
Boiling Point:
155 DEG C
Refractive Index:
n20/D 1.476(lit.)
Flash Point:
> 110 C
Water:
0.1 g/100 mL at 19℃
Solubilities:
Appearance:yellow liquid
Transport Information:180kgs
Hazard Symbols:Not regulated UN NO.
particular:particular
Color/Form:
Amber-colored liquid
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents. Thickens and becomes rancid upon prolonged exposure to air.
Storage temp:
Keep tightly closed in a cool place in a tightly closed container.
Computed Properties:
Molecular Weight:138.61578 [g/mol]
Molecular Formula:C4H7ClOS
XLogP3-AA:2.6
H-Bond Donor:0
H-Bond Acceptor:2
Rotatable Bond Count:3
Exact Mass:137.990613
MonoIsotopic Mass:137.990613
Topological Polar Surface Area:42.4
Heavy Atom Count:7
Formal Charge:0
Complexity:64.7
Isotope Atom Count:0
Defined Atom Stereocenter Count:0
Undefined Atom Stereocenter Count:0
Defined Bond Stereocenter Count:0
Undefined Bond Stereocenter Count:0
Covalently-Bonded Unit Count:1
Feature 3D Hydrophobe Count:1
Effective Rotor Count:3
Conformer Sampling RMSD:0.4
CID Conformer Count:38
Safety and Handling
Hazard Codes:
Not regulated UN NO.
Safety:
A human skin and eye irritant. Ingestion of large doses can cause vomiting. When heated to decomposition it emits acrid smoke and irritating fumes.
Skin, Eye, and Respiratory Irritations:
Lachrymator.
Cleanup Methods:
Soak up pooled liquid with a suitable neutralizing absorbent, such as dry calcium hydroxide. Exercise caution during the neutralization as considerable heat may be generated. Place the absorbed material into a suitable chemical waste container. Apply diethanolamine (DEA) to the spill area and allow to stand for 5 min. Using wet towels, wipe up the DEA. Flush the spill area to remove residual DEA.
Transport:
180kgs
Fire Fighting Procedures:
Use water, dry chemicals, foam or carbon dioxide. If drums are not leaking, keep cooled with a water spray. High pressure water hose may spread product from broken containers increasing contamination hazards. Use of contaminated buildings, areas and equipment must be prevented until they are properly decontaminated.
Fire Potential:
This material is considered combustible.
Formulations/Preparations:
The pesticide products, which appear to be vernolate and pebulate, are marketed by Stauffer under the trade names Vernam and PEBC, respectively.
Reactivities and Incompatibilities:
This material is acidic in nature and is not compatible with strong bases or water. It reacts with amino-, amido-, hydroxyl- or mercapto groups.
Protective Equipment and Clothing:
Lachrymator.
Octanol/Water Partition Coefficient:
0.1 (est).
Use and Manufacturing
Use and Manufacturing:
U.S. Production

1-10 million pounds produced in 1977; current annual production is 1-10 million pounds.
Usage:
As linseed oil in paints, for salad oil blends, in hydrogenated state as shortening, dietary supplement.
Environmental Fate and Exposure Potential
Environmental Fate/Exposure Summary:
Atmospheric: photolysis and hydrolysis in water droplets should rapidly destroy the cmpd in the atmosphere.
S-(n-propyl) chlorothioformate is likely to have minimal environmental release. The manufacture of the cmpd should take place in a closed system. Use of this cmpd as an intermediate in preparation of pesticides is likely to also occur in a closed system.
Atmospheric: ... based on its estimated volatility the cmpd could move into the atmosphere.
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