벤조트리아졸

벤조트리아졸
벤조트리아졸 구조식 이미지
카스 번호:
95-14-7
한글명:
벤조트리아졸
동의어(한글):
1,2,3-트리아자인덴;벤젠아지미드;벤즈이소트리아졸;아즈1H-BENZOTRIAZOLE;2,3-디아자인돌;벤조트리아졸;아지미도벤젠;1,2,3-벤조트리아졸;아지미도벤젠;벤젠아지미드;2,3-디아자인돌;벤조트라이아졸
상품명:
1H-Benzotriazole
동의어(영문):
BENZOTRIAZOLE;1H-Benzo[d][1,2,3]triazole;1,2,3-BENZOTRIAZOLE;Benzotriazol;1,2,3-Benztriazole;1H-Benzotriazol;1,2,3-Benzotrialole;1H-1,2,3-BENZOTRIAZOLE;Cobratec;BLS 1326
CBNumber:
CB4467102
분자식:
C6H5N3
포뮬러 무게:
119.12
MOL 파일:
95-14-7.mol
MSDS 파일:
SDS

벤조트리아졸 속성

녹는점
97-99 °C(lit.)
끓는 점
204 °C (15 mmHg)
밀도
1,36 g/cm3
증기 밀도
4.1 (vs air)
증기압
0.04 mm Hg ( 20 °C)
굴절률
1.5589 (estimate)
인화점
170 °C
저장 조건
Store below +30°C.
용해도
19g/L
물리적 상태
분말, 과립, 결정, 바늘 또는 플레이크
산도 계수 (pKa)
1.6(at 20℃)
색상
흰색에서 노란색-베이지색
수소이온지수(pH)
6.0-7.0 (100g/l, H2O, 20℃)suspension
냄새
약간의 독특한 냄새
폭발한계
2%
수용성
에 용해됨물 25g/l(20ºC)
Merck
14,1108
BRN
112133
안정성
안정적이지만 빛에 민감할 수 있습니다. 강한 산화제, 중금속과 호환되지 않습니다.
InChIKey
QRUDEWIWKLJBPS-UHFFFAOYSA-N
LogP
1.34 at 22.7℃
CAS 데이터베이스
95-14-7(CAS DataBase Reference)
NIST
1H-Benzotriazole(95-14-7)
EPA
1,2,3-Benzotriazole (95-14-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi,F
위험 카페고리 넘버 20/22-36-52/53-5-36/37/38-20/21/22-11
안전지침서 26-36/37-61-45-36/37/39-28A
유엔번호(UN No.) 2811
WGK 독일 1
RTECS 번호 DM1225000
자연 발화 온도 400 °C
위험 참고 사항 Harmful/Irritant
TSCA Yes
HS 번호 29339990
유해 물질 데이터 95-14-7(Hazardous Substances Data)
독성 LD50 orally in Rabbit: 560 mg/kg LD50 dermal Rabbit > 2000 mg/kg
기존화학 물질 KE-02732
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, 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:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
2 2

벤조트리아졸 MSDS


1H-Benzotriazole

벤조트리아졸 C화학적 특성, 용도, 생산

화학적 성질

yellow to beige solid or Colorless needle-like crystals. Slightly soluble in cold water, ethanol and ether.

용도

1H-Benzotriazole is an anticorrosive agent, which is useful in aircraft deicing and antifreeze fluids. It is also employed in dishwasher detergents. Further, it is used as a restrainer in photographic emulsions and also useful as a reagent for the determination of silver in analytical chemistry. It also serves as a corrosion inhibitor in the atmosphere and underwater. Further, it is utilized in the synthesis of amines from glyoxal.

정의

ChEBI: 1H-Benzotriazole is the simplest member of the class of benzotriazoles that consists of a benzene nucleus fused to a 1H-1,2,3-triazole ring. It has a role as an environmental contaminant and a xenobiotic.

제조 방법

1H-Benzotriazole is prepared by the reaction of o-phenylenediamine with nitrous acid in dilute sulfuric acid. Damschrodner and Peterson were able to synthesize the 1H-benzotriazole in a high yield (80%) by nitrosation of o-phenylenediamine with sodium nitrite in glacial acetic acid and water.
Synthesis of 1H-benzotriazole via diazotization of o-phenylenediamine
Synthesis of 1H-benzotriazole via diazotization of o-phenylenediamine
Reaction: Add o-phenylenediamine to 50°C water to dissolve, then add glacial acetic acid, cool down to 5°C, add sodium nitrite to stir the reaction. The reactant gradually turned dark green, the temperature rose to 70-80 ℃, the solution turned orange-red, placed at room temperature for 2 hours, cooled, filtered out the crystals, washed with ice water, dried to obtain the crude product, the crude product was distilled under reduced pressure, and collected 201 -204°C (2.0kPa) fraction, and then recrystallized with benzene to obtain 1H-Benzotriazole products with a melting point of 96-97°C, with a yield of about 80%.

주요 응용

1H-Benzotriazole (BT) is a chemical used in a wide variety of industrial, commercial, and consumer products. It main used as an anticorrosive in metalworking, in art restoration, and as a tarnish remover and protective coating in the construction industry.
In the aircraft industry, 1H-benzotriazole and tolyl benzotriazole are found to be the primary agents in most types of aircraft deicing/antiicing fluid (ADAFs).
Benzotriazole is also used as a component of aircraft deicing fluid, pickling inhibitor in boiler scale removal, restrainer, developer and antifogging agent in photographic emulsions, corrosion inhibitor for copper, chemical intermediate for dyes, in pharmaceuticals, and as fungicide. (HSDB 1998).
Benzotriazole(BTA), ethylenediamine tetraaceticacid(EDTA), and potassium iodide(KI) were used for preparing the polishing slurries.

일반 설명

White to light tan crystals or white powder. No odor.

공기와 물의 반응

Dust may form an explosive mixture in air. Slightly soluble in water.

반응 프로필

The triazoles are a group of highly explosive materials that are sensitive to heat, friction, and impact. Sensitivity varies with the type substitution to the triazole ring. Metal chelated and halogen substitution of the triazol ring make for a particularly heat sensitive material. Azido and nitro derivatives have been employed as high explosives. No matter the derivative these materials should be treated as explosives.

위험도

Highly toxic by ingestion. May explode under vacuum distillation.

건강위험

ACUTE/CHRONIC HAZARDS: When heated to decomposition 1H-Benzotriazole emits toxic fumes. 1H-Benzotriazole can react violently during vacuum distillation.

화재위험

Flash point data are not available for 1H-Benzotriazole. 1H-Benzotriazole is probably combustible.

Safety Profile

Poison by intravenous route.Moderately toxic by ingestion and intraperitoneal routes.Questionable carcinogen with experimental tumorigenicdata. Mutation data reported. May detonate at 220°C or during vacuum distillation. When heated to decompositionit

잠재적 노출

Because benzotriazoles are used in large quantities as a corrosion inhibitor, it is mainly through this type of use that benzotriazoles become an environmental contaminant. As a corrosion inhibitor and fire retardant, they are used in antifreeze in concentrations of 0.01-2.0% and in airplane deicing/antiicing fluids in unknown concentrations, up to 10% (Cancilla et al.,1997). Used antifreeze may leak or be poured down drains and thence enters the environment. Also, an estimated 80% of aircraft deicing/anti-icing fluids are deposited on the ground due to spray drift, jet blast, and wind shear during taxiing and takeoff, according to a recent study (Hartwell et al., 1995).

Carcinogenicity

Chronic (2-year) feeding studies were conducted. Rats were given 0, 6700, or 12,000 ppm in feed for 78 weeks and held for an additional 26 weeks. Mice were given 0, 11,700, or 23,500 ppm in feed in 104 weeks. The authors concluded that under the conditions shown in this study, there were no convincing evidence that 1-H-benzotriazole was carcinogenic in rats or mice.

Purification Methods

1,2,3-Benzotriazole crystallises from toluene, CHCl3, Me2NCHO or a saturated aqueous solution, and is dried at room temperature or in a vacuum oven at 65o. Losses are less if the material is distilled in a vacuum. CAUTION: may EXPLODE during distillation; necessary precautions must be taken. [Damschroder & Peterson Org Synth Coll Vol III 106 1955, Beilstein 26 III/IV 93.]

벤조트리아졸 준비 용품 및 원자재

원자재

준비 용품


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