o-ジアニシジン

Dianisidine

HCID 8411CAS 119-90-4

基本情報

標準SMILES
COc1cc(-c2ccc(N)c(OC)c2)ccc1N
InChIKey
JRBJSXQPQWSCCF-UHFFFAOYSA-N
分子式
C14H16N2O2
平均分子量
244.29 g/mol
単同位体質量
244.12117775

概要

3,3'-Dimethoxybenzidine (o-Dianisidine) can cause cancer according to an independent committee of scientific and health experts.

名称と識別子

優先名称
Dianisidine
IUPAC
4-(4-amino-3-methoxyphenyl)-2-methoxyaniline
現地名
o-ジアニシジン
英語名
o-Dianisidine
分子式
C14H16N2O2
分子量
244.29

名称と別名

o-Dianisidine3,3'-DIMETHOXYBENZIDINE119-90-4DianisidineBlue Base NBFast Blue B BaseCellitazol BMitsui Blue B Baseortho-DianisidineAzogene Fast Blue BDiacel Navy DCNeutrosel navy bn
名称をさらに表示
o-ジアニシジン3,3’-ジメトキシベンジジンジアニシジン3,3’ジメトキシベンジジン3,3'-ジネトキシベンジジン3,3'-ジメトキシベンジジンo-ジアニシジン [生化学用]4,4'-ジアミノ-3,3'-ジメトキシビフェニルファストブルーB3,3'-ジメトキシベンジジン (別名:ジアニシジン)3,3′‐ジメトキシベンジジン3,3′‐ジメトキシベンジジン標準品O-ジアニシジン, 98+%3,3'-ジメトキシベンジジン, 10 µg/mL in Ethyl acetate3,3'-ジメトキシベンジジン, 100 µg/mL in AcCN3,3'-ジメトキシベンジジン, 1000 µg/mL in AcCN3,3′-ジメトキシ-4,4′-ビフェニルジアミン4,4′-ビ(2-メトキシアニリン)4,4′-ビ[2-メトキシアニリン]カンバミンブルーB3,3'-Dimethoxy-[1,1'-biphenyl]-4,4'-diamineai3-00864c.i.24110bluebasenbbluebnbaseC.I. 24110
Disperse Black 6Blue BN BaseBlue Base irga BSpectrolene Blue BFast Blue Base BLake Blue B Baseo-DianisidinaDiato Blue Base B

データベース識別子

CAS
119-90-4
PubChem CID
8411
DTXSID
DTXSID3025091
ChEMBL
CHEMBL398363
ChEBI
CHEBI:82321
UNII
MJY508JZXV
EC Number
204-355-4
Nikkaji
J3.253K

物性

構造計算による物性

XLogP
2.2
極性表面積
70.5 Ų
水素結合供与体数
2
水素結合受容体数
4
回転可能結合数
3
重原子数
18

実験および物理化学的性質

Chemical Classes · 2 件

Hazardous Air Pollutants (HAPs)

Carcinogens

PolymersNitrogen Compounds -> Amines, Polyaromatic
pHWEAK BASE
LogP · 3 件

log Kow = 1.81

1.81

1.81

Color/Form · 2 件

LEAFLETS OR NEEDLES FROM WATER

Colorless crystals that turn a violet color on standing.

Solubility · 6 件

less than 0.1 mg/mL at 68 °F (NTP, 1992)

Sol in alc, benzene, ether

Sol in chloroform, acetone

PROBABLY SOL IN MOST ORG SOLVENTS AND LIPIDS

In water, 60 mg/l @ 25 °C

Solubility in water, g/100ml at 25 °C: 0.006

物理化学的性質

融点
137 · 137-138 °C(lit.)
沸点
387.21 °C · 387.21°C (rough estimate)
比重(密度)
1.1079 · 1.1079 (rough estimate)
屈折率
1.6 · 1.6000 (estimate)
闪点
403 °F · 403 °F
貯蔵温度
Store at RT.
化学的性質 · 1 件

化学的特性o-Dianisidine, crystallizes dimorphically, rarely in needles, with mp 133°C , often in flakes with mp 137-138°C . It forms colorless crystals, but commercial products have a tinge of violet. It is sparingly soluble in water but soluble in alcohol, ether, and benzene. One gram of ethyl acetate dissolves 0.285 g of o-dianisidine at 73°C . The pure compound is stable upon exposure to air, but commercial products turn violet. o-Dianisidine is resistant to water but sensitive to oxidizing agents.

安全と法規制

GHS分類

GHS Classification · 6 件

Danger

H302: Harmful if swallowed [Warning Acute toxicity, oral]

P203, P264, P270, P280, P301+P317, P318, P330, P405, and P501 (click each P-code to see the statement)

Danger

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P203, P264, P270, P280, P301+P317, P318, P330, P405, and P501 (click each P-code to see the statement)

危険有害性情報

Regulatory Information · 3 件

Chemical: [1,1'-Biphenyl]-4,4'-diamine, 3,3'-dimethoxy-

Hazard Traits - Carcinogenicity

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - Benzidine congeners: Human health tier II assessment
DOT LabelPoison
Fire Hazards · 2 件

This chemical is combustible. (NTP, 1992)

Combustible. Gives off irritating or toxic fumes (or gases) in a fire.

Fire PotentialCombustible when exposed to heat or flame.
Health HazardsExcerpt from NIOSH Pocket Guide for o-Dianisidine:

安全と保護具

Fire Fighting · 2 件

Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. A water spray may also be used. (NTP, 1992)

Use water spray, dry powder, carbon dioxide.

First Aid Measures · 4 件

Fresh air, rest.

Remove contaminated clothes. Rinse and then wash skin with water and soap.

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Rinse mouth. Refer for medical attention .

First Aid · 2 件

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

(General first aid procedures)

Safe StorageSeparated from oxidants and food and feedstuffs. Well closed.
Fire Fighting ProceduresWATER, CARBON DIOXIDE, DRY CHEMICAL.
Storage Conditions · 1 件

PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. /Chemical Carcinogens/

毒性情報

Cancer Sites[in animals: bladder, liver, stomach & mammary gland tumors]
Target OrgansSkin, kidneys, liver, thyroid, liver
Environmental Fate · 3 件

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 230(SRC), determined from a log Kow of 1.81(2) and a regression-derived equation(3), indicates that 3,3'-dimethoxybenzidine is expected to have moderate mobility in soil(SRC). The first pKa of 3,3'-dimethoxybenzidine is estimated as 4.2(SRC), using an estimation method based on perturbed molecular orbital theory and linear free energy (LFER) methods(4). This estimated pKa indicates that 3,3'-dimethoxybenzidine will partially exist in the protonated form under acidic conditions and cations have greater adsorption to soils than neutral molecules(SRC). Furthermore, 3,3'-dimethoxybenzidine is an aromatic amine which may form covalent bonds with humic materials resulting in relatively immobile quinone-like complexes(5). Volatilization of the neutral species of 3,3'-dimethoxybenzidine from moist soil surfaces is not expected to be an important fate process(SRC) based upon an estimated Henry's Law constant of 4.7X10-11 atm-cu m/mole(SRC), developed using a fragment constant estimation method(6). The conjugate acid of 3,3-dimethoxybenzidine will not volatilize since cations are non-volatile(SRC). 3,3'-Dimethoxybenzidine is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 1.2X10-7 mm Hg(SRC), determined from a fragment constant method(7). No data were found regarding the biodegradation of 3,3'-dimethoxybenzidine in soils; however, screening studies using sewage sludge inoculum suggest biodegradation will occur slowly in the environment(8,9). Structurally similar compounds such as benzidine are shown to be rapidly oxidized by Fe(III) and other cations which are frequently found in soil(10), which suggest that 3,3'-dimethoxybenzidine may also be degraded by a similar process(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 230(SRC), determined from a log Kow of 1.81(2) and a regression-derived equation(3), indicates that 3,3'-dimethoxybenzidine is expected to adsorb to suspended solids and sediment(SRC). The frist pKa of 3,3'-dimethoxybenzidine is estimated as 4.2(SRC), using an estimation method based on perturbed molecular orbital theory and linear free energy (LFER) methods(4). This estimated pKa indicates that 3,3'-dimethoxybenzidine will partially exist in the protonated form under acidic conditions and cations have greater adsorption to suspended solids and sediment than neutral molecules(SRC). Volatilization of the free base from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 4.7X10-11 atm-cu m/mole(SRC), developed using a fragment constant estimation method(5). The conjugate acid of 3,3'-dimethoxybenzidine will not volatilize since cations are non-volatile(SRC). According to a classification scheme(6), an estimated BCF of 5(SRC), from its log Kow(2) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). No information on the biodegradation of 3,3'-dimethoxybenzidine in natural waters was found(SRC), but this compound was reported to be resistant to biodegradation in the Japanese MITI test(8), suggesting biodegradation in waters will most likely occur slowly(SRC). Structurally similar compounds such as benzidine are shown to be rapidly oxidized by Fe(III) and other cations which are frequently found in environmental waters(9), which suggest that 3,3'-dimethoxybenzidine may also be degraded by a similar process(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 3,3'-dimethoxybenzidine, which has an estimated vapor pressure of 1.2X10-7 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase 3,3'-dimethoxybenzidine is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 3 hours(SRC), calculated from its rate constant of 1.3X10-10 cu cm/molecule-sec at 25 °C (SRC)determined using a structure estimation method(3). Since 3,3'-dimethoxybenzidine absorbs light greater than 290 nm(4), it may be susceptible to direct photolysis in the environment(SRC). Particulate-phase 3,3'-dimethoxybenzidine may be removed from the air by wet and dry deposition(SRC).

Adverse EffectsOccupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Exposure Routes · 2 件

The substance can be absorbed into the body by inhalation, through the skin and by ingestion.

inhalation, skin absorption, ingestion, skin and/or eye contact

Signs and Symptoms · 3 件

Cough.

Redness.

irritation skin; In Animals: kidney, liver damage; thyroid, spleen changes; [potential occupational carcinogen]

法規制情報

RCRA Requirements · 1 件

U091; As stipulated in 40 CFR 261.33, when 3,3'-dimethoxybenzidine, as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to federal and/or state hazardous waste regulations. Also defined as a hazardous waste is any container or inner liner used to hold this waste or any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5(e)).

Atmospheric Standards · 1 件

Listed as a hazardous air pollutant (HAP) generally known or suspected to cause serious health problems. The Clean Air Act, as amended in 1990, directs EPA to set standards requiring major sources to sharply reduce routine emissions of toxic pollutants. EPA is required to establish and phase in specific performance based standards for all air emission sources that emit one or more of the listed pollutants. 3,3'-Dimethoxybenzidine is included on this list.

CERCLA Reportable Quantities · 1 件

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 100 lb or 45.4 kg. The toll free number of the NRC is (800) 424-8802; In the Washington D.C. metropolitan area (202) 426-2675. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

State Drinking Water Guidelines(FL) FLORIDA 250 ug/l

安全データ

wgk
3
tsca
TSCA listed
rtecs
DD0875000
ridadr
2811
毒性
Dianisidine is a probable carcinogen used in the manufacture of dyes. EPA has classified as a Group 2B—probable human carcinogen.
hs_code
29222990

化学と産業

薬理情報

Metabolism/Metabolites · 5 件

BISAZOBIPHENYL DYE DERIVED FROM 3,3'-DIMETHOXYBENZIDINE WAS METABOLIZED TO 3,3'-DIMETHOXYBENZIDINE IN BOTH THE DOG AND RAT. THE N-ACETYL DERIV OF 3,3'-DIMETHOXYBENZIDINE WAS IDENTIFIED IN URINE FROM RATS TREATED WITH DYE DERIVED FROM 3,3'-DIMETHOXYBENZIDINE.

... AFTER ADMIN OF A DOSE OF 1 G O-DIANISIDINE TO 2 DOGS, 0.4% FREE DIAMINE & ... 5% OF A METABOLITE WITH PROPERTIES SIMILAR TO ... 3,3'-DIHYDROXYBENZIDINE WERE EXCRETED IN URINE.

The carcinogenic aromatic amine 3,3'-dimethoxybenzidine was rapidly metabolized in the rat. GC/MS studies of urine and bile demonstrated the presence of 8 previously unidentified metabolites formed via-N-acetylation, hydroxylation, O-demethylation, and glucuronidation.

The conventional Ames assay metabolising system was confirmed to be deficient in its ability to N-acetylate. This may render the test less sensitive to compounds which normally have an acetylation step during their in vivo activation to carcinogens. The addition of acetyl-coenzyme A to the S9 mix in the Ames assay increased the mutagenicity of benzidine in Salmonella typhimurium strains TA98 and TA1538 4-5-fold. This was consistent with the observation that benzidine is N-acetylated prior to deoxyribonucleic acid binding in vivo in rat liver. Two 3,3'-disubstituted benzidines, o-tolidine and o-dianisidine, were also tested. A smaller increase in o-tolidine mutagenicity, compared to that observed with benzidine, occurred with the addition of acetyl-coenzyme A. However, the production of acetylated metabolites from o-tolidine was only 37% of that from benzidine. The mutagenicity of o-dianisidine was unaffected by acetyl-coenzyme A. Acetylation of o-dianisidine was only 16% of that observed with benzidine, and the N-acetyl derivatives of o-dianisidine showed lower mutagenicity than the parent amine.

For more Metabolism/Metabolites (Complete) data for 3,3'-DIMETHOXYBENZIDINE (12 total), please visit the HSDB record page.

Absorption, Distribution and Excretion · 5 件

O-DIANISIDINE HAS BEEN FOUND IN URINE OF WORKERS EXPOSED TO THIS CMPD.

(14)C-labeled 3,3'-dimethoxybenzidine was absorbed through rat skin after application of an acetone soln, and only 29% had disappeared from the application site in 24 hr. It was found in the tissues and excreta.

The carcinogenic aromatic amine 3,3'-dimethoxybenzidine was rapidly metabolized in the rat. Thirty min after iv admin of (14)C-3,3'-dimethoxybenzidine less than 2% of the dose could be recovered from the animal as the parent cmpd. Extensive biliary excretion (70%) resulted in the accumulation of 50% in the intestinal tract. Three days after either oral or iv dosing, 50% of the admin radiolabel had been excreted in the feces and 30-40% excreted in the urine while 45% of the remaining radiolabel was present in the liver in the form of covalently bound metabolites.

... In 1954 /results from laboratory tests indicated/ that skin is principal portal of entry of benzidines. ... It was considered likely that the hydrochloride salt could be absorbed percutaneously. /Benzidines/

For more Absorption, Distribution and Excretion (Complete) data for 3,3'-DIMETHOXYBENZIDINE (6 total), please visit the HSDB record page.

用途と製造

Uses · 6 件

3,3'-Dimethoxybenzidine is used as an intermediate for the production of dyes and pigments.

Used as a chemical intermediate in the production of dyes and dianisidine diisocyanate; Also used to dye leather, paper, plastics, rubber, and textiles; [HSDB]

Pulp and Paper Processing [Category: Industry]

CHEMICAL INTERMEDIATE IN PRODN OF O-DIANISIDINE DIISOCYANATE ... ; FOR DETECTION OF PRESENCE OF THIOCYANATES, NITRITES & A NUMBER OF METALS.

USED IN DYEING LEATHER, PAPER, PLASTIC, RUBBER, TEXTILES

CHEM INT FOR PIGMENTS, EG, PIGMENT ORANGE 16; DYE FOR ACETATE RAYON (FORMER USE)

U.S. Imports · 4 件

(1984) 106,005 lb

(1983) 655,000 lb

(1977) 55,500 lb

(1971) 273,000 lb

U.S. Production(1967) 368,000 lbs
Consumption PatternsESSENTIALLY 100% AS A CHEM INT FOR DYES AND PIGMENTS
Methods of ManufacturingThe methyl ether of o-nitrophenol is reduced by zinc dust and caustic soda to the hydrazo cmpd which is then rearranged with hydrochloric acid.
Formulations/PreparationsIT IS AVAILABLE COMMERCIALLY AS FREE BASE (TECHNICAL AND 99% GRADES) AND AS ITS DIHYDROCHLORIDE.
応用分野 · 3 件

用途医薬?染料(ファーストブルーBベース)中間体

使用o-Dianisidine is a starting material for the production of disazo dyes and pigments. Like benzidine and o-tolidine, o-dianisidine forms colors with numerous oxidizing agents, e.g., copper, cobalt, and gold ions. o-Dianisidine is quantitatively determined by titration with nitrite using potassium iodide and starch paper as the indicator. o-Dianisidine can be detected in the urine using potassium 1,2-naphthoquinone4-sulfonate after extraction. A rapid and easy method is based on the color formed with cyanogen bromide. Its detection limit is 0.05 mg/kg. The free o-dianisidine base and the dihydrochloride are marketed in moist forms with a 10-30% water content.

一般的な説明Colorless crystals or a light brown powder. Turns violet on standing. Carcinogen.

調製方法

製造方法2-Nitroanisole is reduced (H2-catalyst or iron-formic acid) to o-anisidine or (benzidine-type reaction) to o-dianisidine [119-90-4], both of which are important as dye intermediates.

上流・下流製品情報

下流製品

ダイレクトブルー1Direct Blue 1513,3'-ジヒドロキシベンジジン4-ヒドロキシ-3-[[4'-[[1-ヒドロキシ-6-(フェニルアミノ)-3-スルホ-2-ナフチル]アゾ]-3,3'-ジメトキシ-1,1'-ビフェニル-4-イル]アゾ]-1-ナフタレンスルホン酸二ナトリウム3,3′-ジヒドロキシ-1,1′-ビフェニル-4,4′-ジカルボン酸3,3'-[(3,3'-ジメトキシ[1,1'-ビフェニル]-4,4'-ジイル)ビス(アゾ)]ビス[4-ヒドロキシ-1-ナフタレンスルホン酸ナトリウム]1-Naphthalenesulfonic acid, 4-amino-5-hydroxy-6-[[4'-[(4-hydroxyphenyl)azo]-3,3'-dimethoxy[1,1'-biphenyl]-4-yl]azo]-, monosodium salt1,6-Naphthalenedisulfonic acid, 7-[[4'-[(6-amino-1-hydroxy-3-sulfo-2-naphthalenyl)azo]-3,3'-dimethoxy[1,1'-biphenyl]-4-yl]azo]-8-hydroxy-, trisodium salttetrasodium [mu-[[3,3'-[(3,3'-dihydroxy[1,1'-biphenyl]-4,4'-diyl)bis(azo)]bis[4,5-dihydroxynaphthalene-2,7-disulphonato]](8-)]]dicuprate(4-)C.I. Direct Black 87ダイレクトブルー14-アミノ-3-[[4'-[(1-ヒドロキシ-4-スルホ-2-ナフチル)アゾ]-3,3'-ジメトキシ-1,1'-ビフェニル-4-イル]アゾ]-1-ナフタレンスルホン酸二ナトリウム

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