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1-ブタノール

1-ブタノール 化学構造式
71-36-3
CAS番号.
71-36-3
化学名:
1-ブタノール
别名:
1-ブタノール;プロピルカルビノール;ブタン-1-オール;ブチルアルコール;3-メチル-1-プロパノール;3-メチルプロパン-1-オール;4-ブタノール;n-ブタノール;ブタノール;正ブタノール;n-ブチルアルコール;1-ブタノ-ル;1ブタノル;2-ブタノール;n-ブチルアルコール(1-ブタノール);ノルマルブチルアルコール;ノルマルブタノール;1-ブタノール [高速液体クロマトグラフィー用];1-ブタノール [吸光分析用];1‐ブタノール
英語化学名:
1-Butanol
英語别名:
NBA;BuOH;ccs203;n-BuOH;CCS 203;NA 1120;butanols;Butanolo;Hemostyp;n-C4H9OH
CBNumber:
CB9113046
化学式:
C4H10O
分子量:
74.12
MOL File:
71-36-3.mol

1-ブタノール 物理性質

融点 :
-90 °C (lit.)
沸点 :
116-118 °C (lit.)
比重(密度) :
0.81 g/mL at 25 °C (lit.)
蒸気密度:
2.55 (vs air)
蒸気圧:
6.7 hPa (20 °C)
屈折率 :
n20/D 1.399(lit.)
FEMA :
2178 | BUTYL ALCOHOL
闪点 :
95 °F
貯蔵温度 :
Store at +5°C to +30°C.
溶解性:
water: soluble
外見 :
Liquid
酸解離定数(Pka):
15.24±0.10(Predicted)
色:
APHA: ≤10
Relative polarity:
0.586
PH:
7 (70g/l, H2O, 20℃)
臭い (Odor):
Alcohol-like; pungent; strong; characteristic; mildly alcoholic, non residual.
臭気閾値(Odor Threshold):
0.038ppm
爆発限界(explosive limit):
1.4-11.3%(V)
水溶解度 :
80 g/L (20 ºC)
Sensitive :
Moisture Sensitive
極大吸収波長 (λmax):
λ: 215 nm Amax: 1.00
λ: 220 nm Amax: 0.50
λ: 240 nm Amax: 0.10
λ: 260 nm Amax: 0.04
λ: 280-400 nm Amax: 0.01
Merck :
14,1540
JECFA Number:
85
BRN :
969148
Henry's Law Constant:
49.2 at 50 °C, 92.0 at 60 °C, 152 at 70 °C, 243 at 80 °C (headspace-GC, Hovorka et al., 2002)
暴露限界値:
TLV-TWA 300 mg/m3 (100 ppm) (NIOSH), 150 mg/m3 (50 ppm) (ACGIH); IDLH 8000 ppm (NIOSH).
安定性::
Stable. Incompatible with strong acids, strong oxidizing agents, aluminium, acid chlorides, acid anhydrides, copper, copper alloys. Flammable.
CAS データベース:
71-36-3(CAS DataBase Reference)
NISTの化学物質情報:
1-Butanol(71-36-3)
EPAの化学物質情報:
1-Butanol (71-36-3)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  Xn,T,F
Rフレーズ  10-22-37/38-41-67-39/23/24/25-23/24/25-11
Sフレーズ  13-26-37/39-46-7/9-45-36/37-16-7
RIDADR  UN 1120 3/PG 3
WGK Germany  1
RTECS 番号 EO1400000
自然発火温度 649 °F
TSCA  Yes
HSコード  2905 13 00
国連危険物分類  3
容器等級  III
有毒物質データの 71-36-3(Hazardous Substances Data)
毒性 LD50 orally in rats: 4.36 g/kg (Smyth)
消防法 危険物第4類第二石油類(非水溶性)
化審法 (2)-3049 優先評価化学物質
安衛法 有機則 第二種有機溶剤等
絵表示(GHS)
注意喚起語 Danger
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H226 引火性の液体および蒸気 引火性液体 3 警告
H302 飲み込むと有害 急性毒性、経口 4 警告 P264, P270, P301+P312, P330, P501
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 P264, P280, P302+P352, P321,P332+P313, P362
H318 重篤な眼の損傷 眼に対する重篤な損傷性/眼刺激 性 1 危険 P280, P305+P351+P338, P310
H335 呼吸器への刺激のおそれ 特定標的臓器毒性、単回暴露; 気道刺激性 3 警告
H336 眠気やめまいのおそれ 特定標的臓器毒性、単回暴露; 麻酔作用 3 警告 P261, P271, P304+P340, P312,P403+P233, P405, P501
H372 長期にわたる、または反復暴露により臓器の障 害 特定標的臓器有害性、単回暴露 1 危険 P260, P264, P270, P314, P501
注意書き
P233 容器を密閉しておくこと。
P240 容器を接地すること/アースをとること。
P260 粉じん/煙/ガス/ミスト/蒸気/スプレーを吸入しないこ と。
P264 取扱い後は皮膚をよく洗うこと。
P264 取扱い後は手や顔をよく洗うこと。
P270 この製品を使用する時に、飲食または喫煙をしないこ と。
P271 屋外または換気の良い場所でのみ使用すること。
P314 気分が悪い時は、医師の診断/手当てを受けること。
P403+P233 換気の良い場所で保管すること。容器を密閉 しておくこと。
P405 施錠して保管すること。
P501 内容物/容器を...に廃棄すること。

1-ブタノール 価格 もっと(104)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01W0102-0332 1-ブタノール 面積分率99.0+% [CH3(CH2)2CH2OH](GC)
1-Butanol 面積分率99.0+% [CH3(CH2)2CH2OH](GC)
71-36-3 500mL ¥1100 2021-03-23 購入
富士フイルム和光純薬株式会社(wako) W01W0102-0332 1-ブタノール 面積分率99.0+% [CH3(CH2)2CH2OH](GC)
1-Butanol 面積分率99.0+% [CH3(CH2)2CH2OH](GC)
71-36-3 3L ¥4300 2021-03-23 購入
東京化成工業 B0228 1-ブタノール [吸光分析用] >99.0%(GC)
1-Butanol [for Spectrophotometry] >99.0%(GC)
71-36-3 100mL ¥3400 2021-03-23 購入
東京化成工業 B0704 1-ブタノール >99.0%(GC)
1-Butanol >99.0%(GC)
71-36-3 25mL ¥1600 2021-03-23 購入
関東化学株式会社(KANTO) 04354-00 1‐ブタノール >99.0%(GC)
1‐Butanol >99.0%(GC)
71-36-3 500mL ¥1200 2021-03-23 購入

1-ブタノール 化学特性,用途語,生産方法

外観

無色澄明の液体

定義

本品は、次の化学式で表される脂肪族アルコールである。

溶解性

水に可溶 (9.1ml/100ml水, 25℃), アルコール, エーテル, その他多くの有機溶剤と混和。エタノールに極めて溶けやすく、水にやや溶けにくい。

用途

溶剤、有機合成原料。

用途

分光分析用。

用途

塗料溶剤(ロジン、セラック、ダンマル、エステルガム、コーパル、繊維素塗料)、酢酸ブチル原料、安定剤、アルコール精製、果実精DBP(可塑剤)原料、医薬品、MEK、アクリル酸ブチル、化粧品原料(清浄用化粧品、頭髪用化粧品、基礎化粧品、メークアップ化粧品、芳香化粧品、日焼け?日焼け止め化粧品、爪化粧品、アイライナー化粧品、口唇化粧品、口腔化粧品、入浴用化粧品)

化粧品の成分用途

変性剤、溶剤、香料

効能

溶解剤

特徴

1.ノルマルブタノール(NBA)はノルマルブチルアルコールとも呼ばれ、炭素数4の直鎖アルコールです。
2.ノルマルブタノールは水にほとんど溶解せず、ほとんどの有機溶媒に溶解します。

主な用途/役割

ノルマルブタノール(NBA)はノルマルブチルアルコールとも呼ばれ、炭素数4の直鎖アルコールです、は水にほとんど溶解せず、ほとんどの有機溶媒に溶解します。
  1. 塗料樹脂、アクリル酸ブチル、酢酸ブチル等のカルボン酸ブチルエステル、グリコールエーテル等の原料として使用されます。
  2. 様々な有機物をよく溶解することから、溶媒としても広く利用されています。
  3. 溶剤型接着剤、水性型接着剤に使用される。

使用上の注意

不活性ガス封入

説明

n-Butyl alcohol is a colourless flammable liquid with strong alcoholic odour. n-Butyl alcohol is a highly refractive liquid and burns with a strongly luminous flame. It is incompatible with strong acids, strong oxidising agents, aluminium, acid chlorides, acid anhydrides, copper, and copper alloys. n-Butyl alcohol has an extensive use in a large number of industries. For instance, it is used as solvent in industries associated with the manufacturing of paints, varnishes, synthetic resins, gums, pharmaceuticals, vegetable oils, dyes, and alkaloids. n-Butyl alcohol finds its use in the manufacture of artificial leather, rubber, plastic cements, shellac, raincoats, perfumes, and photographic films.

化学的特性

n-Butyl alcohol is a colorless flammable liquid with a strong alcoholic odor. n-Butyl alcohol is a highly refractive liquid and burns with a strongly luminous flame. It is incompatible with strong acids, strong oxidizing agents, aluminium, acid chlorides, acid anhydrides, copper, and copper alloys. n-Butyl alcohol has extensive use in a large number of industries. For instance, it is used as a solvent in industries associated with the manufacturing of paints, varnishes, synthetic resins, gums, pharmaceuticals, vegetable oils, dyes, and alkaloids. n-Butyl alcohol is used in the manufacture of artificial leather, rubber, and plastic cements, shellac, raincoats, perfumes, and photographic films. It is a solvent, chemical intermediate and an additive in unleaded gasoline.

化学的特性

1-Butanol is a colorless, volatile liquid with a rancid sweet odor.
The air odor threshold of 1-butanol was reported to be 0.83 ppm ; others have identified the minimum concentration with identifiable odor as 11 and 15 ppm .

物理的性質

Clear, colorless liquid with a rancid sweet odor similar to fusel oil. Experimentally determined detection and recognition odor threshold concentrations were 900 μg/m3 (300 ppbv) and 3.0 mg/m3 (1.0 ppmv), respectively (Hellman and Small, 1974). Odor threshold concentration in water is 500 ppb (Buttery et al., 1988). The least detectable odor threshold in concentration water at 60 °C was 0.2 mg/L (Alexander et al., 1982). Cometto-Mu?iz et al. (2000) reported nasal pungency threshold concentrations ranging from approximately 900 to 4,000 ppm.

天然物の起源

Reported present in peppermint oil from Brazil, Achillea ageratum, tea, apple aroma, American cranberry, black currants, guava fruit, papaya, cooked asparagus, tomato, Swiss cheese, Parmesan cheese, heated butter, cognac, Armagnac, rum and cider.

使用

Lacquer solvent; manufacture of plastics and rubber cements

使用

1-Butanol is used in the production of butylacetate, butyl glycol ether, and plasticizerssuch as dibutyl phthalate; as a solvent in thecoating industry; as a solvent for extractionsof oils, drugs, and cosmetic nail products;and as an ingredient for perfumes and flavor.
1-Butanol occurs in fusel oil and as aby-product of the fermentation of alcoholicbeverages such as beer or wine. It is presentin beef fat, chicken broth, and nonfilteredcigarette smoke (Sherman 1979).

使用

As solvent for fats, waxes, resins, shellac, varnish, gums etc.; manufacture of lacquers, rayon, detergents, other butyl Compounds; in microscopy for preparing paraffin imbedding materials.

定義

ChEBI: A primary alcohol that is butane in which a hydrogen of one of the methyl groups is substituted by a hydroxy group. It it produced in small amounts in humans by the gut microbes.

定義

Two alcohols that are derived from butane: the primary alcohol butan-1-ol (CH3(CH2)2CH2OH) and the secondary alcohol butan-2-ol (CH3CH(OH)CH2CH3). Both are colorless volatile liquids used as solvents.

調製方法

The principal commercial source of 1-butanol is n-butyraldehyde obtained from the oxo reaction of propylene, followed by hydrogenation in the presence of a catalyst . 1-Butanol has also been produced from ethanol via successive dehydrogenation to acetaldehyde, followed by an aldol process. The earliest commercial route to 1-butanol, which is still used extensively in many Third World countries, employs fermentation of molasses or corn products with Clostridium acetobutylicum .

Aroma threshold values

Detection: 500 ppb to 509 ppm

一般的な説明

Colorless liquid. Used in organic chemical synthesis, plasticizers, detergents, etc.

空気と水の反応

Highly flammable. Soluble in water.

反応プロフィール

1-Butanol attacks plastics. [Handling Chemicals Safely 1980. p. 236]. Mixtures with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. May form explosive butyl hypochlorite by reacting with hypochlorous acid. May form butyl explosive butyl hypochlorite with chlorine.

危険性

Toxic on prolonged inhalation, irritant to eyes. Toxic when absorbed by skin. Flammable, moderate fire risk. Eye and upper respiratory tract irritant.

健康ハザード

The toxicity of 1-butanol is lower than thatof its carbon analog. Target organs are theskin, eyes, and respiratory system. Inhalationcauses irritation of the eyes, nose, and throat.It was found to cause severe injury to rabbits’eyes and to penetrate the cornea uponinstillation into the eyes. Chronic exposureof humans to high concentrations may causephotophobia, blurred vision, and lacrimation.
A concentration of 8000 ppm was maternallytoxic to rats, causing reduced weightgain and feed intake. Teratogenicity wasobserved at this concentration with a slightincrease in skeletal malformations (Nelsonet al. 1989).
In a single acute oral dose, the LD50 value(rats) is 790 mg/kg; in a dermal dose theLD50 value (rabbits) is 4200 mg/kg.
n-Butanol is oxidized in vivo enzymaticallyas well as nonenzymatically and iseliminated rapidly from the body in the urineand in expired air. It inhibits the metabolismof ethanol caused by the enzyme alcoholdehydrogenase.
Based on the available data, the useof n-butanol as an ingredient is consideredsafe under the present practices andconcentrations in cosmetic nail products(Cosmetic, Toiletry and Fragrance Association1987a).

健康ハザード

Exposures to n-butyl alcohol by inhalation, ingestion, and/or skin absorption are harm ful. n-Butyl alcohol is an irritant, with a narcotic effect and a CNS depressant. Butyl alcohols have been reported to cause poisoning with symptoms that include, but are not limited to, irritation to the eyes, nose, throat, and the respiratory system. Prolonged exposure results in symptoms of headache, vertigo, drowsiness, corneal infl amma tion, blurred vision, photophobia, and cracked skin. It is advised that workers com ing in contact with n-butyl alcohol should use protective clothing and barrier creams. Occupational workers with pre-existing skin disorders or eye problems, or impaired liver, kidney or respiratory function may be more susceptible to the effects of the substance.

健康ハザード

Anesthesia, nausea, headache, dizziness, irritation of respiratory passages. Mildly irritating to the skin and eyes.

火災危険

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.

化学反応性

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.

安全性プロファイル

A poison by intravenous route. Moderately toxic by skin Review: Group 3 IMEMDT 7,56,87; Animal Inadequate Evidence IMEMDT 39,67,86* contact, ingestion, subcutaneous, and intraperitoneal routes. Human systemic Reported in EPA TSCA Inventory. Community fight-To-Ihow List. OSHA PEL: TWA 10 pprn Classifiable as a Carcinogen DFG MAK: 2 ppm (11 mg/m3) DOT CLASSIFICATION: 3; Label: Flammable Liquid ingestion, inhalation, skin contact, and intraperitoneal routes. Experimental reproductive effects. A skin and eye irritant. Questionable carcinogen. A flammable fight fire, use foam, CO2, dry chemical. Incompatible with oxidzing materials. When heated to decomposition it emits acrid and irritating fumes. See also ESTERS. effects by inhalation: conjunctiva irritation, unspecified respiratory system effects, and nasal effects. Experimental reproductive Though animal experiments have shown the butyl alcohols to possess toxic properties, they have produced few cases of poisoning in industry, probably because of their low reported to have resulted in irritation of the eyes, with corneal inflammation, slight headache and H2ziness, slight irritation of the nose and throat, and dermatitis about fingers. Keratitis has also been reported. Mutation data reported.

Chemical Synthesis

n-Butyl alcohol is obtained by fermentation of glycerol, mannite, starches, and sugars in general, using Bacillus butylicus sometimes synergized by the presence of Clostridium acetobutryricum; synthetically, from acetylene.

職業ばく露

Butyl alcohols are used as solvents for paints, lacquers, varnishes, natural and synthetic resins, gums, vegetable oils, dyes, camphor, and alkaloids. They are also used as an intermediate in the manufacture of pharmaceuticals and chemicals; in the manufacture of artificial leather, safety glass; rubber and plastic cements, shellac, raincoats, photographic films, perfumes; and in plastic fabrication.

Source

1-Butanol naturally occurs in white mulberries and papaya fruit (Duke, 1992). Identified as one of 140 volatile constituents in used soybean oils collected from a processing plant that fried various beef, chicken, and veal products (Takeoka et al., 1996).

環境運命予測

2Biological. 1-Butanol degraded rapidly, presumably by microbes, in New Mexico soils releasing carbon dioxide (Fairbanks et al., 1985). Bridié et al. (1979) reported BOD and COD values of 1.71 and 2.46 g/g using filtered effluent from a biological sanitary waste treatment plant. These values were determined using a standard dilution method at 20 °C for a period of 5 d. Heukelekian and Rand (1955) reported a similar 5-d BOD value of 1.66 g/g which is 64.0% of the ThOD value of 2.59 g/g. Using the BOD technique to measure biodegradation, the mean 5-d BOD value (mM BOD/mM 1-butanol) and ThOD were 3.64 and 60.7%, respectively (Vaishnav et al., 1987). In activated sludge inoculum, following a 20-d adaptation period, 98.8% COD removal was achieved. The average rate of biodegradation was 84.0 mg COD/g?h (Pitter, 1976).
Photolytic. An aqueous solution containing chlorine and irradiated with UV light (λ = 350 nm) converted 1-butanol into numerous chlorinated compounds which were not identified (Oliver and Carey, 1977).
Reported rate constants for the reaction of 1-butanol and OH radicals in the atmosphere: 6.8 x 10-10 cm3/molecule?sec at 292 K (Campbell et al., 1976), 8.31 x 10-12 cm3/molecule?sec (Wallington and Kurylo, 1987). Reported rate constants for the reaction of 1-butanol and OH radicals in the atmosphere: 8.3 x 10-12 cm3/molecule?sec at 298 K (Atkinson, 1990); with OH radicals in aqueous solution: 2.2 x 10-9 L/molecule?sec (OH concentration 10-17 M) (Anbar and Neta, 1967). Based on an atmospheric OH concentration of 1.0 x 106 molecule/cm3, the reported half-life of 1-butanol is 0.96 d (Grosjean, 1997).
Chemical/Physical. Complete combustion in air yields carbon dioxide and water vapor. Burns with a strongly luminous flame (Windholz et al., 1983).
1-Butanol will not hydrolyze because it has no hydrolyzable functional group (Kollig, 1993).
At an influent concentration of 1,000 mg/L, treatment with GAC resulted in an effluent concentration of 466 mg/L. The adsorbability of the carbon used was 107 mg/g carbon (Guisti et al., 1974).

貯蔵

Store n-butyl alcohol in a cool, dry, well-ventilated location, away from smoking areas. Fire hazard may be acute. Outside or detached storage is preferred. Separate from incompatibles. Containers should be bonded and grounded for transfer to avoid static sparks

輸送方法

UN1120 Butanols, Hazard Class: 3; Labels: 3— Flammable liquid. UN1212 Isobutanol or Isobutyl alcohol, Hazard Class: 3; Labels: 3—Flammable liquid

純化方法

Dry it with MgSO4, CaO, K2CO3, or solid NaOH, followed by refluxing with, and distillation from, small amounts of calcium, magnesium activated with iodine, or aluminium amalgam. It can also be dried with molecular sieves, or by refluxing with n-butyl phthalate or succinate. (For method, see Ethanol.) n-Butanol can also be dried by efficient fractional distillation, water passing over in the first fraction as a binary azeotrope (contains about 37% water). An ultraviolet-transparent distillate has been obtained by drying with magnesium and distilling from sulfanilic acid. To remove bases, aldehydes and ketones, the alcohol is washed with dilute H2SO4, then NaHSO4 solution; esters are removed by boiling for 1.5hours with 10% NaOH. It has also been purified by adding 2g NaBH4 to 1.5L butanol, gently bubbling with argon and refluxing for 1 day at 50o. Then adding 2g of freshly cut sodium (washed with butanol) and refluxed for 1day. Distil and collect the middle fraction [Jou & Freeman J Phys Chem 81 909 1977]. [Beilstein 1 IV 1506.]

Toxicity evaluation

The primary effects observed following oral and inhalation exposure in rats and mice to n-butyl alcohol include neurological and neurodevelopmental effects. n-Butyl alcohol has been evaluated in a large number of experimental animal and in vitro studies examining possible mechanisms for alcoholinduced neurotoxicity. One proposed mechanism is that alcohols, in general, produce neurological changes by disrupting the lipid bilayer. A few experimental animal studies have shown that n-butyl alcohol, like other alcohols, can disrupt membrane integrity. Other in vitro and experimental animal studies have demonstrated that n-butyl alcohol interacts with protein-receptors and modulates their effects such that it potentiates inhibitory g-aminobutyric acid (GABA) and glycine receptors and inhibits excitatory neuronal receptors such a glutamate. This modulatory action of n-butyl alcohol is supportive of the observed neurobehavioral changes (e.g., central nervous system (CNS) depressant profile) associated with n-butyl alcohol exposure in humans.
In addition, experimental animal studies have shown that n-butyl alcohol inhibits fetal rat brain astroglial cell proliferation by disrupting the phospholipase D (PLD) signaling pathway. Inhibition of astroglial cell proliferation, which has been postulated as a mode of action for ethanol-induced microencephaly and mental retardation observed in cases of fetal alcohol syndrome. These mechanisms can also be relevant to the observed dilation in the brain that has been noted in animals gestationally exposed to n-butyl alcohol.

不和合性

Butyl alcohols may form explosive mixture with air. In all cases they are Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Attacks some plastics, rubber and coatings. n-Butanol is incompatible with strong acids; halogens, caustics, alkali metals; aliphatic amines; isocyanates. sec-Butanol forms an explosive peroxide in air. Ignites with chromium trioxide. Incompatible with strong oxidizers; strong acids; aliphatic amines; isocyanates, organic peroxides. tert-Butanol is incompatible with strong acids (including mineral acid), including mineral acids; strong oxidizers or caustics, aliphatic amines; isocyanates, alkali metals (i.e., lithium, sodium, potassium, rubidium, cesium, francium). isoButanol is incompatible with strong acids; strong oxidizers; caustics, aliphatic amines; isocyanates, alkali metals and alkali earth. May react with aluminum at high temperatur

廃棄物の処理

Incineration, or bury absorbed waste in an approved land fill.

1-ブタノール 上流と下流の製品情報

原材料

準備製品


1-ブタノール 生産企業

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71-36-3(1-ブタノール)キーワード:


  • 71-36-3
  • alcoolbutylique(french)
  • butanol(french)
  • Butanol-1
  • Butanolen
  • Butanolo
  • butanols
  • butylalcohol(non-specificname)
  • Butylowy alkohol
  • butylowyalkohol
  • butylowyalkohol(polish)
  • Butyric alcohol
  • butyricalcohol
  • butyricornormalprimarybutylalcohol
  • CCS 203
  • ccs203
  • femanumber2178
  • Hemostyp
  • Methylolpropane
  • NA 1120
  • NBA
  • n-Butan-1-ol
  • n-Butanolbutanolen
  • n-C4H9OH
  • normalprimarybutylalcohol
  • Propylcarbinol
  • Propylmethanol
  • Rcra waste number U031
  • rcrawastenumberu031
  • Tebol 88, 99
  • 1-butanol, hplc grade
  • 1-ブタノール
  • プロピルカルビノール
  • ブタン-1-オール
  • ブチルアルコール
  • 3-メチル-1-プロパノール
  • 3-メチルプロパン-1-オール
  • 4-ブタノール
  • n-ブタノール
  • ブタノール
  • 正ブタノール
  • n-ブチルアルコール
  • 1-ブタノ-ル
  • 1ブタノル
  • 2-ブタノール
  • n-ブチルアルコール(1-ブタノール)
  • ノルマルブチルアルコール
  • ノルマルブタノール
  • 1-ブタノール [高速液体クロマトグラフィー用]
  • 1-ブタノール [吸光分析用]
  • 1‐ブタノール
  • 1-ブタノール 99.9%
  • 1-ブタノール ACS REAGENT,≥99.4%
  • 1-ブタノール PURISS. P.A.,ACS REAGENT,REAG. ISO,REAG. PH. EUR.,≥99.5% (GC)
  • 1-ブタノール クロマソルブ PLUS,FOR HPLC,≥99.7%
  • 1-ブタノールN-ブチルアルコール
  • 分析化学
  • 高速液体クロマトグラフィー用溶剤
  • 構造分類
  • 官能性 & α,ω-二官能性アルカン
  • 溶剤 (HPLC用/吸収スペクトル測定用)
  • 吸収スペクトル測定用溶剤
  • 一官能性アルカン
  • 1-アルカノール
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