붕산트리메틸

붕산트리메틸
붕산트리메틸 구조식 이미지
카스 번호:
121-43-7
한글명:
붕산트리메틸
동의어(한글):
붕산트리메틸;트라이메틸보레이트;트라이메틸보레이트;트라이메틸 보레이트
상품명:
Trimethyl borate
동의어(영문):
trimethyl;TRIMETHOXYBORANE;B(OCH3)3;METHYL BORATE;C3H9BO3;TriMethyl borat;borestero;Borester O;Lobitridol;BORON METHOXIDE
CBNumber:
CB1126251
분자식:
C3H9BO3
포뮬러 무게:
103.91
MOL 파일:
121-43-7.mol
MSDS 파일:
SDS

붕산트리메틸 속성

녹는점
-34 °C (lit.)
끓는 점
68-69 °C (lit.)
밀도
0.932 g/mL at 20 °C (lit.)
증기 밀도
3.59 (vs air)
굴절률
n20/D 1.358(lit.)
인화점
8 °F
저장 조건
Store at <= 20°C.
용해도
테트라히드로푸란, 에테르, 이소포르필아민, 헥산 및 메탄올과 혼합 가능.
물리적 상태
액체
Specific Gravity
0.915
색상
무색의
수용성
물과 반응
감도
Moisture Sensitive
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
Merck
14,9712
BRN
1697939
Dielectric constant
8.2(20℃)
노출 한도
ACGIH: TWA 200 ppm; STEL 250 ppm (Skin)
OSHA: TWA 200 ppm(260 mg/m3)
NIOSH: IDLH 6000 ppm; TWA 200 ppm(260 mg/m3); STEL 250 ppm(325 mg/m3)
안정성
안정적인. 산화제와 호환되지 않습니다. 수분이 있으면 천천히 분해되고 물에서는 빠르게 분해됩니다. 가연성.
InChIKey
WRECIMRULFAWHA-UHFFFAOYSA-N
CAS 데이터베이스
121-43-7(CAS DataBase Reference)
NIST
Boric acid, trimethyl ester(121-43-7)
EPA
Boric acid (H3BO3), trimethyl ester (121-43-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,F,T
위험 카페고리 넘버 11-21-23/25-36/37/38-10-36-61-60
안전지침서 16-27-36/37/39-45-25-23-2-26-53
유엔번호(UN No.) UN 2416 3/PG 2
WGK 독일 3
RTECS 번호 ED5600000
F 고인화성물질 21
TSCA Yes
위험 등급 3
포장분류 II
HS 번호 29209085
유해 물질 데이터 121-43-7(Hazardous Substances Data)
독성 LD50 orally in rats: 6.14 ml/kg (Smyth)
기존화학 물질 KE-03514
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
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H370 장기(또는, 영향을 받은 알려진 모든 장기를 명시)에 손상을 일으킴(노출되어도 특정 표적장기 독성을 일으키지 않는다는 결정적인 노출경로가 있다면 노출경로를 기재) 특정 표적장기 독성 - 1회 노출 구분 1 위험 GHS hazard pictograms P260, P264, P270, P307+P311, P321,P405, P501
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
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.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
3
1 1

붕산트리메틸 MSDS


Trimethyl borate

붕산트리메틸 C화학적 특성, 용도, 생산

화학적 성질

Water-white moisture-sensitive liquid, fumes in the air. It forms an azeotrope with methanol with an azeotrope of 55°C. Miscible with ether, methanol, hexane, tetrahydrofuran; It is stable in anhydrous state and decomposes into methanol and boric acid in presence of water.

용도

Trimethyl borate is a useful reagent in organic synthesis. It is involved in the production of resins, waxes and paints and acts as a methylation agent. As a boron source, it is used to prepare flame retardants, anti-oxidants and corrosion inhibitors. It reacts with Grignard reagents followed by hydrolysis to prepare boronic acid. It is also used as a precursor of borate esters, which finds application in the Suzuki coupling reaction. It is used as neutron detector gas in the presence of a scintillation counter; as a promoter of diborane reactions.

주요 응용

Trimethyl borate reacts with a Grignard reagent or organolithium compounds to yield dimethyl boronates, which upon subsequent aqueous acid treatment afford corresponding boronic acids. The resultant boronic acids or esters are useful intermediates in various cross-coupling reactions such as Suzuki coupling and Chan-Lam coupling. It is also used in the preparation of sodium borohydride.

정의

ChEBI: Trimethyl borate is a member of the class of borate esters obtained by the formal condensation of three equivalents of methanol with boric acid.

제조 방법

The preparation method of trimethyl borate
1. The direct reaction between boric acid and methanol is as follows:
3CH30H+H3B03→B (OCH3) 3+3H20
Usually the trimethyl borate formed in the reaction forms an azeotrope with excess methanol and is distilled out together, and then the trimethyl borate is obtained by separating the azeotrope.
2. The direct reaction between boron oxide and methanol is as follows:
B203+6CH30H→2B (OCH3) 3+3H20
3. Borax, methanol and sulfuric acid are directly reacted, and the reaction formula is :
Na2B4O7.1OH2O+12CH30H+2H2S04→4B (OCH3)3+2NaHS04+17H20

화학 반응

Trimethyl borate B(OCH3)3 is a popular borate ester used in organic synthesis.
borate esters are prepared from alkylation of trimethyl borate:
ArMgBr + B(OCH3 )3 → MgBrOCH3 + ArB(OCH3 )2
ArB(OCH3 )2 + 2H2O → ArB(OH)2 + 2 HOCH3

일반 설명

Trimethyl borate appears as a water-white liquid. Denser than water. Vapors heavier than air. Used as a solvent and fungicide for fruit.

공기와 물의 반응

Highly flammable. Rapidly decomposes in water.

반응 프로필

Borates, such as Trimethyl borate, behave similarly to esters in that they react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters/borates with alkali metals and hydrides.

건강위험

May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

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

Moderately toxic by ingestion, skin contact, and intraperitoneal routes. An eye irritant. A very dangerous fire hazard when exposed to heat, flame, or oxidizers. Moderately explosive when exposed to flame. Will react with water or steam to produce toxic and flammable vapors. To fight fire, use dry chemical, CO2, spray, foam. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS and BORON COMPOUNDS.

Purification Methods

Carefully fractionate the borate through a gauze-packed column. Re-distil and collect it in weighed glass vials and seal them. Keep it away from moisture. It undergoes alkyl exchange with alcohols and forms azeotropes, e.g. with MeOH the azeotrope consists of 70% (MeO)3B and 30% MeOH with b 52-54o/760mm, d 0.87. [Charnley et al. J Chem Soc 2288 1952, Gerrard & Lappert Chem Ind (London) 53 1952, Schlesinger et al. J Am Chem Soc 75 213 1953.] It has also been dried with Na and then distilled. [Beilstein 1 IV 1269.]

붕산트리메틸 준비 용품 및 원자재

원자재

준비 용품


붕산트리메틸 공급 업체

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