테레핀유

테레핀유
테레핀유 구조식 이미지
카스 번호:
8006-64-2
한글명:
테레핀유
동의어(한글):
송정유;터펜틴;테레빈유;테레핀유;테레펜틴;테레펜틴오일;정류된테레펜틴오일;추출된테레펜틴;고무테레펜틴;과산화물가가10mmol/L을초과하는소나무(Pinus)속을스팀증류하여얻은터펜틴;과산화물가가10mmol/L을초과하는터펜틴오일및정제오일;수증기증류된터펜틴(소나무속);터펜틴오일및정류된오일;터펜틴오일및정제오일
상품명:
Turpentine oil
동의어(영문):
FIR OIL;FEMA 3089;turps;THUS GUM;Gum thus;gumspirit;GUM SPIRITS;Turpenitine;-Turpentine;L-TURPENTINE
CBNumber:
CB4380009
분자식:
C12H20O7
포뮬러 무게:
276.283
MOL 파일:
8006-64-2.mol
MSDS 파일:
SDS

테레핀유 속성

녹는점
-55 °C (lit.)
끓는 점
153-175 °C (lit.)
밀도
0.86 g/mL at 25 °C (lit.)
증기 밀도
4.84 (−7 °C, vs air)
증기압
4 mm Hg ( −6.7 °C)
굴절률
n20/D 1.515
FEMA
3089 | TURPENTINE, STEAM DISTILLED (PINUS SPP.)
인화점
86 °F
용해도
에탄올에 용해됨
물리적 상태
액체
Specific Gravity
0.850-0.868
색상
무색의
냄새
매운맛
폭발한계
0.80-6%
optical activity
[α]20/D 40 to +48°
?? ??
테르펜
수용성
물에 불용성
안정성
안정적인. 가연성. 염소, 강산화제와 호환되지 않습니다.
LogP
0.78-6.3 at 20℃
EPA
Turpentine, oil (8006-64-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,N
위험 카페고리 넘버 36/38-43-65-51/53-20/21/22-10
안전지침서 36/37-46-61-62
유엔번호(UN No.) UN 1299 3/PG 3
WGK 독일 2
RTECS 번호 YO8400000
자연 발화 온도 233 °C
위험 등급 3.2
포장분류 III
HS 번호 38051000
유해 물질 데이터 8006-64-2(Hazardous Substances Data)
IDLA 800 ppm
기존화학 물질 KE-35026
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H226 인화성 액체 및 증기 인화성 액체 구분 3 경고
H304 삼켜서 기도로 유입되면 치명적일 수 있음 흡인 유해성물질 구분 1 위험 GHS hazard pictograms
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.
P303+P361+P353 피부(또는 머리카락)에 묻으면 오염된 모든 의복은 벗거나 제거하시오 피부를 물로 씻으시오/샤워하시오.
P331 토하게 하지 마시오.
NFPA 704
3
0

테레핀유 MSDS


Turpentine oil

테레핀유 C화학적 특성, 용도, 생산

개요

Turpentine oil is a kind of fluid isolated from live trees, mainly pines. It consists of terpenes including monoterpenes, alpha-pinene, beta-pinene and some amount of careen, camphene, dipentene, and terpinolene. It can be used as a solvent and as a source of materials for organic synthesis. For its application in solvent, it can be used for thinning oil-based paints that are useful for the manufacturing of varnishes. In organic synthesis, it can be used for the synthesis of fragrant chemical compounds such as camphor, linalool and alpha-terpineol. It can also be used for large-scale synthesis of bundles of aligned carbon nanotubes. It can also be used as natural flavoring agent as food additive. Moreover, it can be used to synthesize pesticide as well as be used to facilitate the endodontic retreatment.

화학적 성질

Turpentine is oleorosin extracted from trees of pinus (pinacae). It is a yellowish, opaque, sticky mass with a characteristic odor and taste. It is used extensively in different industries associated with the manufacturing of polishes, grinding fl uids, paint thinners, resins, degreasing solutions, clearing materials, and ink making.
Turpentine oil
The two primary uses of turpentine in industry are as a solvent and as a source of materials for organic synthesis. As a solvent, turpentine is used for thinning oil-based paints for producing varnishes and as a raw material in the chemical industry.

물리적 성질

Turpentine is the oleoresin from species of Pinus Pinacea trees. The crude oleoresin (gum turpentine) is a yellowish, sticky, opaque mass and the distillate (oil of turpentine) is a colorless, volatile liquid with a characteristic odor. Chemically, it contains: alpha-pinene; betapinene; camphene, monocyclic terpene; and terpene alcohols.

용도

Oil of turpentine is primarily used as a solvent for industrial applications, such as thinner for paints and varnishes. Preparation of carbon nano-spheres (CNSs) by decomposition of turpentine oil has been reported.

생산 방법

Gum turpentine is the steam-volatile fraction of pine tree pitch.Wood turpentine is obtained from waste wood chips or sawdust. Sulfate turpentine is a by-product in paper manufacture.

일반 설명

A clear colorless liquid with a characteristic odor. Flash point 90-115°F. Obtained from naphtha-extraction of pine stumps. Less dense than water and insoluble in water. Hence floats on water. Vapors are heavier than air.

공기와 물의 반응

Highly flammable. Insoluble in water.

반응 프로필

WOOD TURPENTINE reacts with oxidizing agents. Calcium hypochlorite was placed in a turpentine container, thought to be empty. Reaction with the residual turpentine resulted in an explosion within a few minutes [Benson 1967]. Reacts violently with chromic anhydride [Haz. Chem. Data 1967 p. 68]. Reacts with stannic chloride producing heat and sometimes flame [Mellor 7:430 1946-47]. May also react exothermically with reducing agents to produce gaseous hydrogen.

건강위험

Occupational exposures to turpentine cause adverse health effects on absorption through the skin, lungs, and intestine. The vapor of turpentine causes severe irritation to the nose, eyes, and respiratory system has a whole. Aspiration of liquid turpentine causes direct irritation to the lungs and results in pulmonary edema and hemorrhage. It also causes dermatitis, eczema, and hypersensitivity among occupational workers. Splashing of liquid turpentine in the eyes causes corneal burns. Turpentine is also known to cause skin eruption, irritation to the gastrointestinal tract, kidney and bladder damage, delirium, ataxia, and benign skin tumor.

Safety Profile

An experimental poison by intravenous route. Moderately toxic to humans by ingestion. Mildly toxic experimentally by ingestion and inhalation. Human systemic effects by ingestion and inhalation: conjunctiva irritation, other olfactory and eye effects, hallucinations or distorted perceptions, antipsychotic, headache, pulmonary, and kidney changes. A human eye irritant. Irritating to skin and mucous membranes. Can cause serious irritation of kidneys. Questionable carcinogen with experimental tumorigenic data. A common air contaminant. A very dangerous fire hazard when exposed to heat or flame; can react vigorously with oxidizing materials. Avoid impregnation of combustibles with turpentine. Keep cool and ventilated. Spontaneous heating is possible. Moderate explosion hazard in the form of vapor when exposed to flame; can react violently with Ca(OCl)2, Cl2, CrO3, Cr- (OCl)2, SnCl4, hexachloromelamine, trichloromelamine. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

잠재적 노출

Turpentines have found wide use as chemical feedstock for the manufacture of floor, furniture, shoe, and automobile polishes; camphor, cleaning materials; inks, putty, mastics, cutting and grinding fluids; paint thinners; resins, and degreasing solutions. Recently, alpha-and beta-pinenes, which can be extracted, have found use as volatile bases for various compounds. The components d-α-pinene and 3-carene, or their hydroperoxides, may be the cause of eczema and toxic effects of turpentine.

Carcinogenicity

When turpentine was applied to the skin, tumor growth was promoted in the rabbit, but not in the mouse.

운송 방법

UN1299 Turpentine, Hazard Class: 3; Labels: 3- Flammable liquid.

비 호환성

Forms an explosive mixture with air. Violent reaction with strong oxidizers, especially chlorine; chromic anhydride; stannic chloride; chromyl chloride.

폐기물 처리

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

주의 사항

During handling of turpentine, occupational workers should always use protective clothing, rubber gloves, and face masks to avoid adverse health effects to the skin and respiratory tract.

참고 문헌

Kalpana Awasthi, et al. "Large scale synthesis of bundles of aligned carbon nanotubes using a natural precursor: turpentine oil." Journal of Experimental Nanoscience 5.6(2010):498-508.
Bai, Yun. "The general situation of flavor from turpentine oil." China Food Additives (2006).
Pakdel, H, S. Sarron, and C. Roy. "alpha-Terpineol from hydration of crude sulfate turpentine oil. " Journal of Agricultural & Food Chemistry 49.9(2001):4337-41.
Dong-Mei, L. I., et al. "Study on synthesis of high purity α-terpineol from turpentine oil." Modern Chemical Industry (2008).
Armstrong, Henry E. "XXXV.—Studies of the terpenes and allied compounds. The nature of turpentine oils, including that obtained from Pinus khasyana." Journal of the Chemical Society Transactions 59:311-315.
Guilbert, J., et al. "Anti-flatulence treatment and status epilepticus: a case of camphor intoxication." Emergency Medicine Journal Emj 24.12(2007):859.
Qin, Lang, and Y. M. Wang. "Application of Turpentine Oil in Synergist and Pesticide and Its Progress." Fine & Specialty Chemicals (2005).
Kaplowitz, G. J. "Clinical uses of rectified turpentine oil." International Endodontic Journal 29.2(1996):93.

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