도데칸

도데칸
도데칸 구조식 이미지
카스 번호:
112-40-3
한글명:
도데칸
동의어(한글):
N-도데칸;노르말도데칸;도데칸;디헥실;n-도데케인;도데케인;도데케인 (모든 이성질체);두오데칸;비헥실
상품명:
Dodecane
동의어(영문):
N-DODECANE;Dodecan;DUODECANE;n-dodecan;ADAKANE 12;DIHEXYL;ALKANE C12;Twelve alkyl;n-Dodecane min;dodecanenormal
CBNumber:
CB5678167
분자식:
C12H26
포뮬러 무게:
170.33
MOL 파일:
112-40-3.mol
MSDS 파일:
SDS

도데칸 속성

녹는점
-9.6 °C (lit.)
끓는 점
215-217 °C (lit.)
밀도
0.75 g/mL at 25 °C (lit.)
증기 밀도
5.96 (vs air)
증기압
1 mm Hg ( 47.8 °C)
굴절률
n20/D 1.421(lit.)
인화점
181.4 °F
저장 조건
Store below +30°C.
용해도
아세톤, 알코올, 클로로포름, 에테르(Weast, 1986) 및 다양한 탄화수소에 용해됩니다.
물리적 상태
액체
산도 계수 (pKa)
>14 (Schwarzenbach et al., 1993)
Specific Gravity
0.749 (20/4℃)
색상
무색의
냄새
알칸
Odor Threshold
0.11ppm
폭발한계
0.6%(V)
수용성
25 ºC에서 <0.1g/100mL
열전도율
0.135 W/(m·K) at 25 ℃
비열
Cp(liquid): 2.21 J/(g·K), at 25℃
BRN
1697175
Henry's Law Constant
29.7(atmm3/mol) at 25 °C (calculated from water solubility and vapor pressure, Tolls et al., 2002) Interfacial tension
Dielectric constant
2.0(20℃)
화장품 원료 기능
향수
InChI
1S/C12H26/c1-3-5-7-9-11-12-10-8-6-4-2/h3-12H2,1-2H3
InChIKey
SNRUBQQJIBEYMU-UHFFFAOYSA-N
SMILES
CCCCCCCCCCCC
LogP
6.100
표면장력
24.07mN/m at 293.15K
CAS 데이터베이스
112-40-3(CAS DataBase Reference)
NIST
n-Dodecane(112-40-3)
EPA
Dodecane (112-40-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn
위험 카페고리 넘버 65-66
안전지침서 62-60-36
유엔번호(UN No.) NA 1993 / PGIII
WGK 독일 3
RTECS 번호 JR2125000
자연 발화 온도 401 °F
TSCA TSCA listed
위험 등급 CBL
HS 번호 29011090
스토리지 클래스 10 - Combustible liquids
Hazard Classifications Asp. Tox. 1
유해 물질 데이터 112-40-3(Hazardous Substances Data)
독성 mouse,LDLo,intravenous,2672mg/kg (2672mg/kg),BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX),Acta Pharmacologica et Toxicologica. Vol. 37, Pg. 56, 1975.
기존화학 물질 KE-12826
그림문자(GHS): Health Hazard (GHS08)
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H304 삼켜서 기도로 유입되면 치명적일 수 있음 흡인 유해성물질 구분 1 위험
예방조치문구:
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.
P331 토하게 하지 마시오.
P405 밀봉하여 저장하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
2
1 0

도데칸 MSDS


Dodecane

도데칸 C화학적 특성, 용도, 생산

화학적 성질

Dodecane, C12H26, is a flammable, colorless liquid with specific gravity 0.749. It occurs in the paraffin fraction of petroleum. Dodecane is released to the environment by wastewater and spills from laboratory and general use of paraffins, petroleum oils, and tars.

물리적 성질

Clear, colorless liquid with a mild aliphatic hydrocarbon odor. An odor threshold concentration of 620 ppbv was reported by Nagata and Takeuchi (1990).

용도

Dodecane is a component of gasoline and is used as solvent, in organic synthesis, in jet fuel research, as a distillation chaser, and in the rubber and paper processing industries.

생산 방법

Dodecane is isolated from the kerosene and gas oil fractions of crude oil by selective adsorption and subsequent desorption to yield mixtures of paraffins that can be separated by fractional distillation.

정의

ChEBI: A straight-chain alkane with 12 carbon atoms. It has been form the essential oils of various plants including Zingiber officinale (ginger).

일반 설명

Clear colorless liquid.

공기와 물의 반응

Flammable. Insoluble in water.

반응 프로필

Saturated aliphatic hydrocarbons, such as Dodecane, may be incompatible with strong oxidizing agents like nitric acid. Charring of the hydrocarbon may occur followed by ignition of unreacted hydrocarbon and other nearby combustibles. In other settings, aliphatic saturated hydrocarbons are mostly unreactive. They are not affected by aqueous solutions of acids, alkalis, most oxidizing agents, and most reducing agents. When heated sufficiently or when ignited in the presence of air, oxygen or strong oxidizing agents, they burn exothermically to produce carbon dioxide and water.

화재위험

Dodecane is combustible.

Carcinogenicity

Dodecane has been shown to be a promoter of skin carcinogenesis for benzo[a]pyrene and ultraviolet radiation.

환경귀착

Biological. Dodecane may biodegrade in two ways. The first is the formation of dodecyl hydroperoxide which decomposes to 1-dodecanol. The alcohol is oxidized forming dodecanoic acid. The other pathway involves dehydrogenation to 1-dodecene, which may react with water, giving 1-dodecanol (Dugan, 1972).
Estimated half-lives of dodecane (0.3 μg/L) from an experimental marine mesocosm during the spring (8–16 °C), summer (20–22 °C), and winter (3–7 °C) were 1.1, 0.7, and 3.6 d, respectively (Wakeham et al., 1983).
Chemical/Physical. Complete combustion in air yields carbon dioxide and water. Dodecane will not hydrolyze because it has no hydrolyzable functional group.

Purification Methods

Pass it through a column of Linde type 13X molecular sieves. Store it in contact with, and distil it from sodium. Pass through a column of activated silica gel. It has been crystallised from diethyl ether at -60o. Unsaturated dry material which remained after passage through silica gel has been removed by catalytic hydrogenation (Pt2O) at 45lb/in2 (3.06 atmospheres), followed by fractional distillation under reduced pressure [Zook & Goldey J Am Chem Soc 75 3975 1953]. It has also purified by partial crystallisation from the melt. [Beilstein 1 IV 498.]

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