아니시딘

아니시딘
아니시딘 구조식 이미지
카스 번호:
90-04-0
한글명:
아니시딘
동의어(한글):
O-아니시딘;아니시딘;2-메톡시벤젠아민;2-메톡시아닐린;2-아미노아니솔;o-메톡시아닐린
상품명:
o-Anisidine
동의어(영문):
2-METHOXYANILINE;ORTHO ANISIDINE;2-ANISIDINE;2-Methoxybenzenamine;2-Methoxy-phenylamine;nsc3122;ai3-08584;O-ANISOLE;2-Anisidin;O-ANISIDINE
CBNumber:
CB1286995
분자식:
C7H9NO
포뮬러 무게:
123.15
MOL 파일:
90-04-0.mol
MSDS 파일:
SDS

아니시딘 속성

녹는점
3-6 °C(lit.)
끓는 점
225 °C(lit.)
밀도
1.092 g/mL at 25 °C(lit.)
증기압
<0.1 at 25 °C (NIOSH, 1994)
굴절률
n20/D 1.574(lit.)
인화점
210 °F
저장 조건
Refrigerator
용해도
14g/L
물리적 상태
분말/고체
산도 계수 (pKa)
4.52(at 25℃)
색상
회백색
수소이온지수(pH)
7.3 (1g/l, H2O, 20℃)
수용성
13g/L(20℃)
감도
Light Sensitive
Merck
14,667
BRN
386210
Henry's Law Constant
1.25 at 25 °C (approximate - calculated from water solubility and vapor pressure)
노출 한도
Potential occupational carcinogen. NIOSH REL: TWA 0.5 mg/m3, IDLH 50 mg/m3; OSHA PEL: TWA 0.5 mg/m3; ACGIH TLV: TWA 0.1 ppm (adopted).
Dielectric constant
5.2300000000000004
안정성
안정적인. 강산화제, 산무수물, 클로로포르메이트, 산, 일부 플라스틱, 고무와 호환되지 않습니다. 공기에 민감합니다.
InChIKey
VMPITZXILSNTON-UHFFFAOYSA-N
LogP
1.180
CAS 데이터베이스
90-04-0(CAS DataBase Reference)
NIST
Benzenamine, 2-methoxy-(90-04-0)
IARC
2A (Vol. Sup 7, 73, 127)
EPA
o-Anisidine (90-04-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,Xi
위험 카페고리 넘버 45-23/24/25-68
안전지침서 53-45
유엔번호(UN No.) UN 2431 6.1/PG 3
WGK 독일 3
RTECS 번호 BZ5410000
F 고인화성물질 8
TSCA Yes
위험 등급 6.1
포장분류 III
HS 번호 29222200
유해 물질 데이터 90-04-0(Hazardous Substances Data)
독성 Acute oral LD50 for rats 2,000 mg/kg, wild birds 422 mg/kg, mice 1,400 mg/kg, rabbits 870 mg/kg (quoted, RTECS, 1985).
IDLA 50 mg/m3
기존화학 물질 KE-23211
중점관리물질 필터링 별표1-36
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H341 유전적인 결함을 일으킬 것으로 의심됨 (노출되어도 생식세포 유전독성을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 생식세포 변이원성 물질 구분 2 경고 P201,P202, P281, P308+P313, P405,P501
H350 암을 일으킬 수 있음 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 1A, 1B 위험 GHS hazard pictograms
예방조치문구:
P201 사용 전 취급 설명서를 확보하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
NFPA 704
1
0

아니시딘 MSDS


o-Anisidine

아니시딘 C화학적 특성, 용도, 생산

개요

o-Anisidine was produced commercially in the United States from the 1920s until late 1950s. By 2009, worldwide only six industries manufactured o-anisidine, but none produced hydrochloride salt. o-Anisidine was available from 44 suppliers, including 20 US suppliers, and the hydrochloride salt was available from eight suppliers, including five US suppliers. US imports of o-anisidine and its hydrochloride salt are reported in the category ‘o-anisidines, p-anisidines, and p-phenetidine,’ and US exports are reported in the category ‘anisidines, dianisidines, phenetidines, and their salts.’ From 1989 to 2008, imports ranged from a high of over 4.6 million kg in 1996 to zero in 2007 and 2008, and exports ranged from zero to 262 000 kg. Reports filed under the US Environmental Protection Agency’s (EPA) Toxic Substances Control Act Inventory Up Rule indicated that United States production plus imports of o-anisidine totaled 500 000 lb–1 million lb in 1986, 1990, and 2006; 1 million–10 million lb in 1990 and 1998; and 10 000–500 000 lb in 2002.

화학적 성질

Anisidine exists as ortho-, meta-, and paraisomers. They have characteristic amine (fishy) odors.
o-Anisidine (or o-methoxyaniline) is an aromatic amine with a methoxyl group ortho to the amino group of aniline. It is a colorless to yellowish, pink, or reddish liquid.o-Anisidine is soluble in water and mineral oils, and miscible with alcohol, benzene, acetone, and diethylether. o-Anisidine hydrochloride, a salt of o-anisidine, is a grayish crystalline solid or powder at room temperature and is soluble in water (NTP, 2011).

물리적 성질

Colorless, yellow to reddish liquid with an amine-like odor. Becomes brown on exposure to air.

용도

Similar to other aromatic amines, o-anisidine may cause methemglobinemia and cancer in humans. It is used mainly as an intermediate for the production of azo dyes and pigments. Other industrial uses of o-anisidine include synthesis of other dyes and pharmaceuticals, as a corrosion inhibitor for steel, and as an antioxidant for polymercaptan resins (IARC, 1999; HSDB, 2012).
Intermediate for azo dyes and for guaiacol.

일반 설명

Clear, yellowish to reddish or brown liquid with an amine (fishy) odor.

공기와 물의 반응

o-Anisidine darkens on exposure to air. Insoluble in water.

반응 프로필

o-Anisidine is sensitive to heat. o-Anisidine is also sensitive to exposure to light. o-Anisidine is incompatible with strong oxidizers. o-Anisidine is also incompatible with acids, acid chlorides, acid anhydrides and chloroformates. o-Anisidine will attack some forms of plastics, rubber and coatings. .

위험도

Strong irritant. Toxic when absorbed through the skin. Possible carcinogen.

건강위험

o-Anisidine was carcinogenic in experimental animals.

화재위험

o-Anisidine is combustible.

Safety Profile

Confirmed carcinogen. Moderately toxic by ingestion. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

잠재적 노출

Anisidines are used in the manufacture of azo dyes; pharmaceuticals; textile-processing chemicals Incompatibilities: 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 coatings and some forms of plastic and rubber.

Carcinogenicity

o-Anisidine is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity in experimental animals.

환경귀착

Biological. o-Anisidine should be biodegradable according to OECD guidelines (Brown and Labouerer (1983). Chemical/Physical. At influent concentrations (pH 3.0) of 10, 1.0, 0.1, and 0.01 mg/L, the GAC adsorption capacities were 52, 20, 7.8, and 3.0 mg/g, respectively. At pHs 7 and 9, the GAC adsorption capacities were 110, 50, 23, and 10 mg/g at influent concentrations of 10, 1.0, 0.1, and 0.01 mg/L, respectively (Dobbs and Cohen, 1980).

운송 방법

UN2431 Anisidines, Hazard Class: 6.1; Labels: 6.1-Poisonous materials

Purification Methods

It is separated from the m-and p-isomers by steam distillation. It is also separated from its usual synthetic precursor o-nitroanisole by dissolving it in dilute HCl (pH <2.0) extracting the nitro impurity with Et2O, adjusting the pH to ~8.0 with NaOH, extracting the amine into Et2O or steam distilling. Extract the distillate with Et2O, dry the extract (Na2SO4), filter, evaporate and fractionate the residual oil. Protect the almost colourless oil from light which turns it yellow in color. [Biggs & Robinson J Chem Soc 3881961, Nodzu et al. Yakugaku Zasshi (J Pharm Soc Japan) 71 713, 715 1951, Beilstein 13 IV 806.]

폐기물 처리

Dissolve in combustible solvent (alcohols, benzene, etc.) and spray solution into furnace equipped with afterburner and scrubber, or burn spill residue on sand and soda ash absorbent in a furnace.

아니시딘 준비 용품 및 원자재

원자재

준비 용품


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