1-프로판올

1-프로판올
1-프로판올 구조식 이미지
카스 번호:
71-23-8
한글명:
1-프로판올
동의어(한글):
1-프로판올;n-프로필알코올;노말-프로필알콜;에틸칼비놀(EthylCarbinol),프로필알콜(PropylAlcohol),프로파놀(Propanol),N-프로파놀(N-Propanol),1-하이드록시프로판(1-Hydroxypropane),1-프로파놀(1-Propanol),프로필릭알콜(PropylicAlcohol),1-프로필알콜(1-PropylAlcohol),;N-프로판올;노말프로필알코올;프로필알코올;노말-프로필알콜
상품명:
1-Propanol
동의어(영문):
PROPANOL;N-PROPANOL;PROPAN-1-OL;Propyl alcohol;N-PROPYL ALCOHOL;Propanol-1;1-Propyl alcohol;PROPANE-1-OL;n-Propan-1-ol;n-C3H7OH
CBNumber:
CB9854149
분자식:
C3H8O
포뮬러 무게:
60.1
MOL 파일:
71-23-8.mol
MSDS 파일:
SDS

1-프로판올 속성

녹는점
-127 °C(lit.)
끓는 점
97 °C(lit.)
밀도
0.804 g/mL at 25 °C(lit.)
증기 밀도
2.1 (vs air)
증기압
10 mm Hg ( 147 °C)
FEMA
2928 | PROPYL ALCOHOL
굴절률
n20/D 1.384(lit.)
인화점
59 °F
저장 조건
Store at +5°C to +30°C.
용해도
H2O: 테스트 통과
물리적 상태
액체
산도 계수 (pKa)
>14 (Schwarzenbach et al., 1993)
색상
<10(APHA)
냄새
에틸알코올과 비슷합니다.
상대극성
0.617
수소이온지수(pH)
7 (200g/l, H2O, 20℃)
폭발한계
2.1-19.2%(V)
Odor Threshold
0.094ppm
?? ??
알코올 중독자
수용성
녹는
최대 파장(λmax)
λ: 220 nm Amax: ≤0.40
λ: 240 nm Amax: ≤0.071
λ: 275 nm Amax: ≤0.0044
Merck
14,7842
JECFA Number
82
BRN
1098242
Henry's Law Constant
6.75 (static headspace-GC, Merk and Riederer, 1997)
노출 한도
TLV-TWA (200 ppm); (500 mg/m3); STEL 250 ppm (625 mg/m3); IDLH 4000 ppm.
Dielectric constant
20.1(25℃)
안정성
안정적인. 공기와 접촉하면 과산화물을 형성할 수 있습니다. 알칼리 금속, 알칼리 토류, 알루미늄, 산화제, 니트로 화합물과 호환되지 않습니다. 가연성이 높습니다. 증기/공기 혼합물은 폭발성이 있습니다.
LogP
0.33
CAS 데이터베이스
71-23-8(CAS DataBase Reference)
NIST
1-Propanol(71-23-8)
EPA
1-Propanol (71-23-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F,Xi
위험 카페고리 넘버 11-41-67
안전지침서 7-16-24-26-39
유엔번호(UN No.) UN 1274 3/PG 2
WGK 독일 1
RTECS 번호 UH8225000
F 고인화성물질 10-23
자연 발화 온도 700 °F
TSCA Yes
위험 등급 3
포장분류 II
HS 번호 29051200
유해 물질 데이터 71-23-8(Hazardous Substances Data)
독성 LD50 orally in rats: 1.87 g/kg (Smyth)
IDLA 800 ppm
기존화학 물질 KE-29362
그림문자(GHS): GHS 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
H225 고인화성 액체 및 증기 인화성 액체 구분 2 위험 GHS hazard pictograms P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H318 눈에 심한 손상을 일으킴 심한 눈 손상 또는 자극성 물질 구분 1 위험 GHS hazard pictograms P280, P305+P351+P338, P310
H336 졸음 또는 현기증을 일으킬 수 있음 특정표적장기 독성 물질(1회 노출);마취작용 구분 3 경고 P261, P271, P304+P340, P312,P403+P233, P405, P501
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P233 용기를 단단히 밀폐하시오. 용기는 환기가 잘 되는 곳에 단단히 밀폐하여 보관하시오.
P240 용기와 수용설비를 접지 및 접합시키시오.
P241 폭발 방지용 장비[전기적/환기/조명/...]을(를) 사용하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
3
1 0

1-프로판올 MSDS


Propan-1-ol

1-프로판올 C화학적 특성, 용도, 생산

물성

물과는 임의의 비율로 혼합되지만, 염화칼슘의 찬 포화 용액에는 녹지 않으므로 에틸알코올과 구별된다. 에틸알코올, 에테르에도 임의의 비율로 혼합된다. 산화하면 프로피온알데히드가 되며 다시 프로피온산이 된다. 황산에 의해 탈수하면 프로필렌이 되며 여기에 요오드화수소를 첨가한 후 가수 분해하면 이소프로필알코올을 생성한다 240~250℃로 수산화칼륨을 작용시키면 프로피온산과 프로필렌이 된다. 브롬과는 반응하여 1, 1-디브로모프로피온알데히드와 브롬화프로필을 생성하며 요오드와 수산화칼륨에서는 요오도포름을 생성한다.

합성

염화에틸마그네슘과 트리히드록시메틸렌을 반응시킨다. 또 프로피온알데히드를 환원해도 좋다. 공업적으로는 천연물에서 분별 증류로 얻어지며 메틸알코올 합성의 부산물로서 얻어진다.

포장, 보관 및 운송

n- 프로판올은 실온에서 휘발성이다. 저장 및 운송은 화재 원인을 피하기 위해 제한되어야합니다. 제한된 저온 보존과 수송 탱커.

개요

1-propanol is the compound with the hydrogen atom in the propane molecules being replaced by hydroxyl group. Because the hydroxyl group can substitute the hydrogen atoms contained in the carbons in the two terminals of carbon chain or middle carbon, thus generating two isomers, n-propyl alcohol and isopropyl alcohol.
The chemical property of the 1-propanol is similar to that of ethanol. It is the byproduct during the process of the methanol synthesis from carbon monoxide and hydrogen. At room temperature and normal pressure, it appears as colorless transparent liquid with fragrance odor. In industry, it is prepared through the reaction between ethylene, carbon monoxide and hydrogen under high pressure and cobalt catalysis; alternatively through the hydration of propylene under the action of sulfate or through the catalytic hydrogenation of acetone. It is commonly used as a solvent with irritating effect on the eyes and mucosa. Inhalation of propyl alcohol steam can lead to dizziness, headache and vomiting, etc.

화학적 성질

1-Propanol is a clear, colorless liquid with an alcoholic odor and a characteristic ripe, fruity flavor. It is soluble in water and miscible with organic solvents (Propanols). It has better dissolution properties than ethanol for fats and oils, and dissolves polar resins in the same way as ethanol. Cellulose nitrate and poly(vinyl acetate) are, however, almost insoluble. For economic reasons propanol is of only limited use as a solvent, and is a starting material for esters.

물리적 성질

Colorless liquid with a mild, alcohol-like odor. Experimentally determined detection and recognition odor threshold concentrations were <75 μg/m3 (<31 ppbv) and 200 μg/m3 (81 ppbv), respectively (Hellman and Small, 1974). An odor threshold concentration of 100 ppbv was reported by Nagata and Takeuchi (1990).

출처

Reported found in the natural aromas of apple, cognac and rum; also formed during alcoholic fermentation. Also reported found in apple, apricot, banana, sweet cherry, papaya, pineapple, orange juice, lingonberry, cranberry, grapes, peas, pineapple, raspberry, strawberry, onion, leek, tomato, ginger, vinegar, many cheeses, butter, fatty fish, fish oil, cooked beef, mutton and pork, beer, several types of bread, pear brandy, Scotch blended whiskey, malt whiskey, cognac, armagnac, weinbrand rum, bourbon whiskey, Irish whiskey, rum, grape wines, cider, sherry, cocoa, tea, roasted filberts and peanuts, honey, soybean, oats, passion fruit, plum, beans, mushroom, apple and plum brandy, gin, rice, rice bran, quince, prickly pear, jackfruit, sake, buckwheat, loquat, wild rice, anise brandy, endive, truffle, arrack, clam, cape gooseberry and Chinese quince.

용도

1-Propanol is used in making n-propyl acetate; and as a solvent for waxes, resins, vegetable oils, and flexographic printing ink. It is produced from the fermentation and spoilage of vegetable matter.

주요 응용

The propanols are used mainly as solvents for coatings; in antifreeze compositions and household and personal products; and as chemical intermediates for the production of esters, amines, and other organic derivatives. As a solvent, 1-propanol is used principally in printing inks, paint, cosmetics, pesticides, cellulose esters and insecticides.
1-Propanol is used commercially to produce glycol ethers. These are characterized by dual functionality, which imparts high solvency, chemical stability, and water compatibility.

제조 방법

1-Propanol is produced commercially by the oxo process by reacting ethylene with carbon monoxide and hydrogen in the presence of a catalyst to give propionaldehyde, which is then hydrogenated. 1-Propanol [71-23-8] is the major product of catalytic reduction of propanal (→Propanols). Reduction is carried out most economically by a continuous vapor-phase process over a heterogeneous catalyst of supported reduced nickel, copper, and/or zinc and manganese metals.

정의

ChEBI: 1-Propanol is the parent member of the class of propan-1-ols that is propane in which a hydrogen of one of the methyl groups is replaced by a hydroxy group. It has a role as a protic solvent and a metabolite. It is a short-chain primary fatty alcohol and a member of propan-1-ols.

일반 설명

N-propanol appears as a clear colorless liquid with a sharp musty odor like rubbing alcohol. Flash point 53-77 °F. Autoignites at 700 °F. Vapors are heavier than air and mildly irritate the eyes, nose, and throat. Density approximately 6.5 lb / gal. Used in making cosmetics, skin and hair preparations, pharmaceuticals, perfumes, lacquer formulations, dye solutions, antifreezes, rubbing alcohols, soaps, window cleaners, acetone and other chemicals and products.

공기와 물의 반응

Highly flammable. Water soluble.

반응 프로필

1-Propanol reacts with alkali metal, nitrides and strong reducing agents to give flammable and/or toxic gases. Reacts with oxoacids and carboxylic acids to form esters plus water. Converted by oxidizing agents to propanal or propionic acid. May initiate the polymerization of isocyanates and epoxides. Incompatible with strong oxidizing agents .

위험도

Flammable, dangerous fire risk. Explosive limits in air 2–13%. Toxic by skin absorption. Eye and upper respiratory tract irritant. Questionable carcinogen.

건강위험

Target organs: skin, eyes, gastrointestinal tracts, and respiratory system. Toxic routes: ingestion, inhalation, and skin contact.
LD50 value, oral (rats): 5400 mg/kg (NIOSH1986)
LD50 value, skin (rabbits): 6700 mg/kg(NIOSH 1986)
Ingestion causes headache, drowsiness,abdominal cramps, gastrointestinal pain,ataxia, nausea, and diarrhea. Eye contactproduces irritation. It may cause dermatitison repeated skin contact. Although thetoxicity of 1-propanol is low, at a highconcentration it may produce a narcoticeffect, as well as irritation of the eyes, nose,and throat..

화재위험

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Safety Profile

Poison by subcutaneous route. Moderately toxic by inhalation, ingestion, intraperitoneal, and intravenous routes. A skin and severe eye irritant. Questionable carcinogen with experimental carcinogenic data. Mutation data reported. A flammable liquid and dangerous fire hazard when exposed to heat, flame, or oxidizers. Explosive in the form of vapor when exposed to heat or flame. Ignites on contact with potassium-tert- butoxide. Dangerous upon exposure to heat or flame; can react vigorously with oxidizing materials. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

잠재적 노출

n-Propyl alcohol is used as as solvent in lacquers, dopes; to make cosmetics; dental lotions; clea- ners, polishes, and pharmaceuticals; as a surgical antiseptic. It is a solvent for vegetable oils, natural gums and resins; rosin, shellac, certain synthetic resins; ethylcellulose, and butyral; as a degreasing agent; as a chemical intermediate.

Carcinogenicity

Eighteen Wistar rats were dosed by oral gavage with 0.3 mL/kg twice weekly. The average survival time was 570 days. In addition to severe liver injury and hyperplasia of the hematopoietic parenchyma, 5 malignant tumors (2 myeloid leukemias, 2 liver sarcomas, and 1 liver cell carcinoma) and 10 benign tumors were observed. Three benign but no malignant tumors were found in the controls given saline.

환경귀착

Biological. In activated sludge inoculum, following a 20-d adaptation period, 98.8% COD removal was achieved. The average rate of biodegradation was 71.0 mg COD/g?h (Pitter, 1976). Using the BOD technique to measure biodegradation, the mean 5-d BOD value (mM BOD/mM 1- propanol) and ThOD were 2.70 and 60.0%, respectively (Vaishnav et al., 1987).
Photolytic. Reported rate constants for the reaction of 1-propanol and OH radicals in the atmosphere: 2.3 x 10-12 cm3/molecule?sec at 300 K (Hendry and Kenley, 1979); 2.3 x 10-9 L/molecule?sec (second-order) at 292 K (Campbell et al., 1976), 5.33 x 10-12 cm3/molecule?sec at 296 K (Overend and Paraskevopoulos, 1978). Based on an atmospheric OH concentration of 1.0 x 106 molecule/cm3, the reported half-life of 1-propanol is 1.5 d (Grosjean, 1997).
Chemical/Physical. At an influent concentration of 1,000 mg/L, treatment with GAC resulted in an effluent concentration of 811 mg/L. The adsorbability of the carbon used was 38 mg/g carbon (Guisti et al., 1974).

운송 방법

UN1274, n-Propanol, Hazard Class: 3; Labels: 3-Flammable liquid.

비 호환성

Vapors may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, perox- ides, permanganates, perchlorates, chlorine, bromine, fluo- rine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. n-Propanol reacts with alkali metal, nitrides and strong reducing agents to give flammable and/ or toxic gases. Reacts with oxoacids and carboxylic acids to form esters plus water. Converted by oxidizing agents to propanal or propionic acid. May initiate the polymerization of isocyanates and epoxides

폐기물 처리

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

1-프로판올 준비 용품 및 원자재

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