Turpentine
- CAS NO.:9005-90-7
- Molecular Weight: 0
- MDL number: MFCD00147790
- EINECS: 232-688-5
- Update Date: 2024-05-21 13:52:30
What is Turpentine?
Absorption
Turpentine is readily absorbed from GI tract, skin, and respiratory tract.
Toxicity
Human : TCLo ( Inhalation) 175ppm, Effects : lung, Thorax or Respiration Human: TCLo ( inhalation ) 6gm/m3/3h , Effects : Behavioral: Headache Infant: LDLo ( Oral ) 1748 mg/kg, Effect : GI, Nausea or vomiting Man: LDLo (Oral ) 3mg/kg Mouse LC50 ( inhalation ) 29mg/m3/2h Mouse: LD50 ( intravenous ) 1180ug/kg Rabbit: LDLo ( Skin) 5010mg/kg, Effect: general depressed activity
Chemical properties
Balsam turpentine is the oleo-gum-resin obtained by incisions made on the trunks of several trees belonging to the genus Pinus. The common American turpentine comes from P. palustris. Crude turpentine contains 75 to 90% resin and 10 to 25% oil. It is of paramount importance to use special techniques in making incisions, because the tree otherwise may die in a short time. A gum (gum turpentine) consisting of white incrustations is formed around the incisions in the tree. Rosin is the resinous residue of the distillation of turpentine. There are several varieties of rosin, varying in color from the palest amber to nearly black and from translucent to opaque, depending on the turpentine source. Colophony is the name of the common rosin variety. The part used is the oleo-gum-resin (turpentine balsam). Turpentine has a penetrating and characteristic odor and a pungent, bitter taste.
Physical properties
Turpentine is a clear, flammable liquid, with a pungent odor and a bitter taste. It is immiscible with water and has a boiling point above 150 °C. Turpentine is a mixture of organic compounds, mainly terpenes, and its composition can vary considerably according to the species of pine from which it is derived. Fractional distillation of turpentine allows the isolation of α-pinene and β-pinene.
The Uses of Turpentine
Turpentine is a mixture of substances called terpenes, primarily pinene. Gum turpentine is extracted from pine pitch; wood turpentine, from wood chips. It has had greater home than industrial use as a solvent. It is irritating and anesthetic and is one of the few solvents that causes allergic contact dermatitis. The incidence of sensitization varies with the type of pine, being generally higher with European than American pines. Owing to the frequency of allergic dermatitis, the availability of turpentine is now extremely limited. One recent study suggested that occupational paternal exposure to turpentine was associated with neuroblastoma in offspring.
Indications
Turpentine has been used experimentally in a bath for the treatment of disseminated sclerosis and sexual dysfunction. It also has been studied for its antibacterial activity and inhibition of osteoclast activity. Turpentine is utilized in experimental models of inflammation to induce a systemic inflammatory immune response in animals.
Background
Turpentine, also known as spirit of turpentine, oil of turpentine, and wood turpentine, is a liquid extracted from live trees, mainly pine, through distillation of resin. It is used as a solvent and base material in organic synthesis reactions. Turpentine is composed of terpenes, mainly the monoterpenes alpha-pinene and beta-pinene with lesser amounts of carene, camphene, dipentene, and terpinolene.
Definition
A yellow viscous resin obtained from coniferous trees. It can be distilled to produce turpentine oil (also known simply as turpentine), used in medicine and as a solvent in paints, polishes, and varnishes.
Definition
turpentine: An oily liquid extractedfrom pine resin. It contains pinene,C10H16, and other terpenes and ismainly used as a solvent.
Composition
Turpentine is primarily composed of monoterpene hydrocarbons (pinenes, camphene and 3-carene). Rosin contains primarily diterpene resin acids, such as abietic acid, dehydroabietic acid, palustric acid and isopimaric acid. P. elliottii turpentine contains around 60% of α-pinene and 30% of β-pinene. P. radiata turpentine generally contains more than 95% of total pinene, of which over half is β-pinene. 3-Carene, which is found in significant proportions in the turpentine of some Pinus species (such as P. roxburghii and P. sylvestris), is of little value and even if it is present in relatively small amounts it may be undesirable for certain applications.
Health Hazard
Recommended Personal Protective Equipment: Organic canister or air-supplied mask; goggles or face shield; rubber gloves; Symptoms Following Exposure: Vapors cause headache, confusion, respiratory distress. Liquid irritates skin. If ingested, can irritate the entire digestive system and may injure kidneys. If liquid is taken into lungs, causes several pneumonitis; General Treatment for Exposure: INHALATION: remove victim to fresh air; call a doctor; administer artificial respiration and oxygen if required. INGESTION: give water and induce vomiting; call a doctor. EYES: flush with water for at least 15 min. SKIN: wipe off, wash with soap and water; Toxicity by Inhalation (Threshold Limit Value): 100 ppm; Short-Term Exposure Limits: 200 ppm for 30 min.; Toxicity by Ingestion: Grade 2, LD50 = 0.5-5 g/kg; Late Toxicity: None; Vapor (Gas) Irritant Characteristics: Vapor causes a slight smarting of the eyes or respiratory system if present in high concentration. The effect is temporary; Liquid or Solid Irritant Characteristics: Minimum hazard. If spilled on clothing and allowed to remain, may be cause smarting and reddening of the skin; Odor Threshold: Data not available.
Chemical Reactivity
Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Pharmacokinetics
Turpentine oil, when inhaled, may help reduce congestion. When used on the skin, turpentine oil may cause warmth and redness that can help relieve pain in the tissue underneath.
Metabolism
Not Available
Properties of Turpentine
Boiling point: | 154-170°C |
Density | 0.86 |
FEMA | 3088 | TURPENTINE GUM (PINUS SPP.) |
Flash point: | 35°C |
Odor | Aromatic, rather unpleasant, penetrating. |
EPA Substance Registry System | Turpentine (9005-90-7) |
Safety information for Turpentine
Computed Descriptors for Turpentine
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium THOMAIND PAPER PH 2.0 TO 4.5 1 BOX BUFFER CAPSULE PH 9.2 - 10 CAP SODIUM CHLORIDE 0.1N CVS ALLOXAN MONOHYDRATE 98% PLATINUM 0.5% ON 3 MM ALUMINA PELLETS (TYPE 73) LITHIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
You may like
-
1-Methyl-6-oxo-1,6-dihydropyridazine-3-carbonitrile 98%View Details
99903-60-3 -
88491-46-7 98%View Details
88491-46-7 -
1823368-42-8 98%View Details
1823368-42-8 -
2-(3-(tert-butyl)phenoxy)-2-methylpropanoic acid 1307449-08-6 98%View Details
1307449-08-6 -
Ethyl 3-(furan-2-yl)-3-hydroxypropanoate 25408-95-1 98%View Details
25408-95-1 -
2-Chloro-5-fluoro-1-methoxy-3-methylbenzene 98%View Details
1805639-70-6 -
1784294-80-9 98%View Details
1784294-80-9 -
Lithium ClavulanateView Details
61177-44-4