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3,4-Dimethylphenol

HCID 7249
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기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
95-65-8
표준 SMILES
Cc1ccc(O)cc1C
InChIKey
YCOXTKKNXUZSKD-UHFFFAOYSA-N
분자식
C8H10O
평균 분자량
122.16 g/mol
단동위원소 질량
122.07316494

개요

3,4-dimethylphenol appears as colorless to light tan crystalline powder or solid. Odor threshold 1.2 mg/L. Taste threshold 0.05 mg/L. (NTP, 1992)

이름 및 식별자

우선 이름
3,4-Dimethylphenol
IUPAC
3,4-dimethylphenol
영어명
3,4-Xylenol
분자식
C8H10O
분자량
122.1644

이름 및 동의어

3,4-DIMETHYLPHENOL95-65-83,4-Xylenol4,5-DimethylphenolPhenol, 3,4-dimethyl-1,3,4-Xylenol1-Hydroxy-3,4-dimethylbenzene4-Hydroxy-1,2-dimethylbenzene3,4-DMPAsym-O-XylenolFEMA No. 3596DTXSID4024062
이름 더 보기
4-Hydroxy-o-xylene1,2-Dimethyl-4-hydroxybenzeneAI3-015524L479F5JU6NSC-1549DTXCID004062CHEBI:39839AS-O-XYLENOL

데이터베이스 식별자

CAS
95-65-8
PubChem CID
7249
DTXSID
DTXSID4024062
ChEMBL
CHEMBL192008
ChEBI
CHEBI:39839
UNII
4L479F5JU6
EC Number
202-439-5
Nikkaji
J43.457D

물성

구조 계산 물성보충 중

XLogP
2.2
극성 표면적
20.2 Ų
수소 결합 공여자 수
1
수소 결합 수용자 수
1
회전 가능 결합 수
0
무거운 원자 수
9
형식 전하
0
복잡도
90.6

실험 및 물리화학적 성질

Chemical ClassesOther Classes -> Phenols
DrugsPharmaceuticals -> Listed in ZINC15
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
FragrancesFragrance Ingredient (3,4-Xylenol) -> IFRA transparency List
PesticidesPesticide -> EPA IRIS
LogP · 3건

log Kow= 2.23

2.23

2.37

Taste0.05 mg/l (taste threshold concn)
Food AdditivesFLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Density · 2건

0.983 at 68 °F (NTP, 1992) - Less dense than water; will float

0.983 @ 20 °C/4 °C

Flavoring AgentsEU Flavoring substances
Viscosity3.00 mN.s.m-2 at 80 °C

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 6건

Danger

H301: Toxic if swallowed [Danger Acute toxicity, oral]

P260, P262, P264, P270, P273, P280, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P361+P364, P363, P391, P405, and P501 (click each P-code to see the statement)

Danger

H301 (99.7%): Toxic if swallowed [Danger Acute toxicity, oral]

P260, P261, P262, P264, P264+P265, P270, P272, P273, P280, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P330, P333+P317, P361+P364, P362+P364, P363, P391, P405, and P501 (click each P-code to see the statement)

유해성 정보

Regulatory Information · 5건

Chemical: Phenol, 3,4-dimethyl-

Commission Regulation (EC) No 1565/2000 (Repealed by Com. Implementing Reg. (EU) No 872/2012)

Phenol, 3,4-dimethyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Phenol, 3,4-dimethyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 17-12-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/30340

3,4-Dimethylphenol: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationIMAP assessments - Xylenols: Human health tier II assessment
DOT LabelPoison
Fire HazardsFlash point data for this chemical are not available. It is probably combustible. (NTP, 1992)
Health Hazards · 1건

SYMPTOMS: Symptoms of exposure to this compound may include burning sensation, coughing, wheezing, laryngitis, and shortness of breath. Other symptoms may include severe irritation or burning of the eyes and skin; irritation of the respiratory system; dizziness, stomach pain, exhaustion, and coma. It can cause headaches, nausea, and vomiting. It can also cause corrosion of the mucous membranes, upper respiratory tract, skin, and eyes. Inhalation may be fatal as a result of spasm, inflammation and edema of the larynx and bronchi; chemical pneumonitis; and pulmonary edema. Chronic exposure may cause liver or kidney damage.

화학 및 산업

약리 정보

Metabolism/Metabolites · 5건

HYDROXYLATION OF AROMATIC HYDROCARBONS WAS STUDIED FOLLOWING THEIR ORAL ADMINISTRATION TO RATS THAT ALSO RECEIVED A PURIFIED DIET CONTAINING NEOMYCIN TO REDUCE THE LEVELS OF NORMALLY OCCURRING SIMPLE URINARY PHENOLS. PHENOLIC METABOLITES WERE QUANTITATIVELY ESTIMATED IN HYDROLYZED URINE SAMPLES BY GAS CHROMATOGRAPHY. AFTER THE ADMIN OF 100 MG/KG OF O-XYLENE IN RATS, 0.1% WAS METABOLIZED TO 3,4-DIMETHYLPHENOL.

YIELDS 4,5-DIMETHYLCATECHOL IN RABBITS. YIELDS 3,4-DIMETHYLPHENYL-BETA-D-GLUCURONIDE IN RABBITS. /FROM TABLE/

YIELDS 3,4-DIMETHYLPHENYL SULFATE IN RABBITS & IN RATS. /FROM TABLE/

FOUR PERSONS WERE EXPOSED TO XYLENES. 2,3- AND 3,4-XYLENOL WERE OBSERVED IN URINE OF THOSE EXPOSED TO O-XYLENE. 2,4-XYLENOL OBSERVED AFTER M-XYLENE AND 2,5-XYLENOL AFTER P-XYLENE.

2,3-Dimethylphenol is a known human metabolite of o-xylene.

Absorption, Distribution and Excretion · 1건

Associations between o-cresol, p-cresol, m-cresol, 2,4-xylenol, 2,5-xylenol, 3,4-xylenol, and 3,5-xylenol exposure levels and urinary phenol excretion were examined in the coke facility industry. The subjects consisted of 76 exposed workers employed in the tar distillation process and 34 controls. ... Urinary metabolite levels were corrected for specific gravity and creatinine. The time weighted average exposure concentrations in the breathing zones of the tar distillation workers were ... 0.02 to 0.04 mg/cu m for xylenols. ... The urinary xylenol levels of exposed workers ranged from 0.12 to 0.97 mg/l with specific gravity correction. In control urine samples, the specific gravity corrected xylenol concentrations ranged from 25 x 10(-3) to 43 x 10(-3) mg/l. Significant correlations were observed between the ambient levels and urinary concentrations of phenol, o-cresol, and the xylenols, with coefficients ranging from 0.45 to 0.82. The author concludes that the biological monitoring of urinary xylenols may be used as a means of measuring xylenol exposure in coke facility workers.

Cellular LocationsCytoplasm

용도 및 제조

Uses · 3건

관련 반응

109건
반응 기록 만들기
HRID 93463 반응식
HRID 93463반응물로Training data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 105689 반응식
HRID 105689반응물로Training data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 132006 반응식
HRID 132006반응물로uspto-grants-2008_06
HRID 134033 반응식
HRID 134033반응물로Training data from https://doi.org/10.1039/C8SC04228D (9/10)
HRID 136257 반응식
HRID 136257반응물로Training data from https://doi.org/10.1039/C8SC04228D (9/10)
HRID 157183 반응식
HRID 157183반응물로Training data from https://doi.org/10.1039/C8SC04228D (9/10)
HRID 228523 반응식
HRID 228523반응물로uspto-grants-2009_07
HRID 228686 반응식
HRID 228686반응물로uspto-grants-2009_07
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Color/Form · 2건

Needles from water

Prisms from ligroin

Hazards Summary · 1건

Safe when used as a flavoring agent in food; [JECFA] Causes tetany, hepatitis, and renal tubular changes in lethal-dose feeding studies of rats; [RTECS] Toxic by ingestion; [HSDB] Corrosive to tissues; May cause spasm, inflammation, and edema of the larynx and bronchi after inhalation; Can cause liver and kidney damage; [CAMEO] May cause burns; [eChemPortal: ESIS] A corrosive substance that can cause injury to the skin, eyes, and respiratory tract; Inhalation may cause chemical pneumonitis; May be absorbed through skin; Effects in high-dose animal studies include acute tubular necrosis and hepatitis; [MSDSonline] As the six dimethylphenol isomers and the mixed isomer substance are generally similar in toxicity, a common TLV for these substances is appropriate. . . . In mice, oral exposure to 250 mg/kg/day produced changes in blood parameters including statistically significant decreases in mean corpuscular volume and mean corpuscular hemoglobin concentration (4 and 3% reduction in mean values, respectively. . . . Available data on skin sensitization from exposure to dimethylphenol are mixed but warrant the addition of a DSEN notation. . . . All six dimethylphenol isomers were tested in a mouse local lymph node assay and the results found 2.4, 2,5, and 3,4-dimethylphenol to be positive for skin sensitization. There are no epidemiology studies. In a case report, ingestion of about 250 ml of a mixture of dimethylphenol isomers resulted in CNS depression, hypotension, and death. [ACGIH] See Phenol.

Reactive GroupPhenols and Cresols
TSCA Requirements · 2건

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. 3,4-Dimethylphenol is included on this list.

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, use, and exposure to EPA as cited in the preamble in 51 FR 41329.

Reactivity Profile3,4-DIMETHYLPHENOL is incompatible with bases, acid chlorides, acid anhydrides, and oxidizing agents. It corrodes steel, brass, copper, and copper alloys. (NTP, 1992)
DOT Emergency Guidelines · 5건

/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Health: TOXIC; inhalation, ingestion, or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution. /Xylenols; Xylenols, liquid; Xylenols, solid/

/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Fire or Explosion: Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors, and sewers explosion hazards. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form. /Xylenols; Xylenols, liquid; Xylenols, solid/

/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Public Safety: CALL Emergency Response Telephone Number ... . As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate enclosed areas. /Xylenols; Xylenols, liquid; Xylenols, solid/

/GUIDE 153: SUBSTANCES - TOXIC AND/OR CORROSIVE (COMBUSTIBLE)/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. /Xylenols; Xylenols, liquid; Xylenols, solid/

For more DOT Emergency Guidelines (Complete) data for 3,4-DIMETHYLPHENOL (8 total), please visit the HSDB record page.

Air and Water ReactionsHygroscopic. Insoluble in water.
Hazard Classes and Categories · 5건

Acute Tox. 3 (99.7%)

Acute toxicity - category 3

Acute toxicity (Oral) - Category 4

Acute toxicity (Oral) - Category 4

Acute Tox. 3 *

안전 및 보호

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1건

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.

Storage ConditionsFIBER DRUMS. /COMMERCIAL MIXTURE/
Nonfire Spill Response · 1건

SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Disposal Methods · 3건

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

The effectiveness of anaerobic filters containing granular activated carbon in treating synthetically prepared wastewaters which contained phenols, polycyclic hydroxy compounds, monocyclic n-aromatics, polycyclic n-aromatics, and aliphatic acids was evaluated. The ability of the activated carbon to retain these compounds along with its external surface, which provides vast sheltered microbial attachment areas, renders activated carbon a very unique medium for anaerobic filter treatment of coal gasification wastewater.

Chemical Treatability of 3,4-Dimethylphenol; Concentration Process: Biological treatment; Chemical Classification: Phenols; Scale of Study: Unknown; Type of Wastewater Used: Pure compound (one solute in a solvent; Results of Study: 95.5% reduction based on chemical oxygen demand; rate of biodegradation 13.4 mg chemical oxygen demand/g hr (activated sludge process).

Isolation and EvacuationExcerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]:
Threshold Limit Values (TLV)1.0 [ppm], inhalable fraction and vapor
Personal Protective Equipment (PPE) · 5건

MINIMUM PROTECTIVE CLOTHING: If Tyvek-type disposable protective clothing is not worn during handling of this chemical, wear disposable Tyvek-type sleeves taped to your gloves.

Some data suggesting breakthrough times /for butyl rubber/ of approximately an hour or more. /Aromatic hydroxyl cmpd/

Breakthrough times /for neoprene/ greater than one hour reported by (normally) two or more testers. /Aromatic hydroxyl cmpd/

Breakthrough times /for polyvinyl alcohol/ less (usually significantly less) than one hour reported by (normally) two or more testers. /Aromatic hydroxyl cmpd/

Wear appropriate chemical protective gloves, boots and goggles.

독성 정보

Body BurdenUrine samples of 35 varnishing workers in six different workplaces contained 3,4-dimethylphenol (0.8 mg/l). The source of this dimethylphenol is probably due to the metabolism of original aromatic components of the varnish(1).
InteractionsA SPONTANEOUSLY DEVELOPING VASOCONSTRICTION IN ISOLATED PERFUSED LUNG AND THE VASOCONSTRICTION CAUSED BY ARTERIALLY INJECTED ATP 50 UG WERE BOTH INHIBITED BY THE ADDITION TO THE PERFUSATE OF VARIOUS PHENOLS INCLUDING 3,4-XYLENOL.
Target OrgansCardiovascular
Ecotoxicity Values · 5건

TLm Carassius carassius (Crucian carp) 21 mg/l/24 hr /Conditions of bioassay not specified/

TLm Rutilus rutilus (roach) 16 mg/l/24 hr /Conditions of bioassay not specified/

TLm Tinca tinca (tench) 18 mg/l/24 hr /Conditions of bioassay not specified/

TLm Salvelinus (trout embryos) 7 mg/l/24 hr /Conditions of bioassay not specified/

For more Ecotoxicity Values (Complete) data for 3,4-DIMETHYLPHENOL (9 total), please visit the HSDB record page.

Environmental Fate · 3건

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 390(SRC), determined from a log Kow of 2.23(2) and a regression-derived equation(3), indicates that 3,4-dimethylphenol is expected to have moderate mobility in soil(SRC). Volatilization of 3,4-dimethylphenol from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.2X10-6 atm-cu m/mole(SRC), determined from its vapor pressure of 0.036 mm Hg(4) and water solubility of 4760 mg/l(5). 3,4-Dimethylphenol is not expected to volatilize from dry soil surfaces based upon a its vapor pressure(3). 3,4-Dimethylphenol has been reported to completely biodegrade in soil in 9 days at a temperature of 19 °C(6).

AQUATIC FATE: Based on a classification scheme(1), a Koc value of 390(SRC), determined from a log Kow of 2.23(2) and a regression-derived equation(3), indicates that 3,4-dimethylphenol is expected to adsorb very little to suspended solids and sediment in water(SRC). 3,4-Dimethylphenol is expected to volatilize from water surfaces(3,SRC) based upon an estimated Henry's Law constant of 1.2X10-6 atm-cu m/mole(SRC), determined from its vapor pressure of 0.036 mm Hg(4) and water solubility of 4760 mg/l(5). Estimated volatilization half-lives for a model river and model lake are 34 days and 250 days, respectively(3,SRC). According to a classification scheme(6), an estimated BCF of 29(3,SRC), from 3,4-dimethylphenol's log Kow(2), suggests bioconcentration in aquatic organisms is low(SRC). In humic waters, degradation by the reaction with peroxy radicals should ensue with a half-life on the order of hours(7). 3,4-Dimethylphenol is not expected to undergo hydrolysis in the environment due to the lack of hydrolyzable functional groups(3). Screening studies indicate that theoretical oxygen demand reached 43% after 5 days(8,9). In addition, it has been reported that 3,4-dimethylphenol was readily degraded in St. Lawrence River water(10). Biodegradation under anaerobic conditions failed to occur after 24 days from a river sediment inoculum(11).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 3,4-dimethylphenol, which has a vapor pressure of 0.036 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 3,4-dimethylphenol 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 4.7 hours(SRC) from its rate constant of 8.14X10-11 cu cm/molecule-sec at 25 °C(3). Atmospheric 3,4-dimethylphenol is known to be removed by rainwater(4). 3,4-Dimethylphenol has an absorption band at 274 nm (water), and a shoulder may extend over 290 nm, thus making it a candidate for direct photochemical degradation(5,6). Night-time degradation in urban areas should occur rapidly through reaction with atmospheric nitrate radicals, as rate constants for this reaction with phenolic compounds are approximately 250 times faster than with hydroxyl radicals(7,SRC).

Food Survey Values3,4-Dimethylphenol was identified as a volatile flavor component of the Japanese dried food, Bonito(1).
Adverse EffectsNeurotoxin - Other CNS neurotoxin
Effluent Concentrations · 1건

3,4-Dimethylphenol was measured in raw waste water from a paper mill at 0.0457 mg/l in 1974, and had been observed at this site in 1972. It was not detected in the treated effluent from the plant(1). 3,4-Dimethylphenol was identified in Los Angeles County, CA effluent (1980-81) at 20 ug/l(2). Waste water from the gasification of Indian Head lignite coal in North Dakota was determined to have an approximate 3,4-dimethylphenol concn of 158 mg/l(3). 3,4-Dimethylphenol was detected in treated refinery effluent (Geelong, Victoria, Australia, 1985) at a concn of 0.02 mg/l(4). 3,4-Dimethylphenol was identified but not quantified in leachate collected from a Swedish municipal landfill in May 1990(5). 3,4-Dimethylphenol was also identified in the leachate from a sanitary landfill in Barcelona, Spain(6).

EPA IRIS Information · 3건

3,4-Dimethylphenol

Cardiovascular

1 x 10 ^-3 mg/kg-day

Soil Adsorption/Mobility · 1건

The Koc of 3,4-dimethylphenol is estimated as 390(SRC), using a log Kow of 2.23(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 3,4-dimethylphenol is expected to have moderate mobility in soil(SRC). 65.2% of 3,4-dimethylphenol was sorbed onto the high clay content, adsorption activated material Bentone 24 at pH= 7.8; 13% with Bentone 18C at pH 7.7; these values fluctuate as a function of pH(4).

Natural Pollution SourcesDimethylphenols, of which 3,4-dimethylphenol is an isomer, are present in the essential oils of various conifers(1), in tea(4,5), in tobacco and tobacco smoke(1-3,5), in roasted coffee and in various smoked foods(5).
Atmospheric Concentrations · 1건

URBAN/SUBURBAN: In 1984, a gas phase concn of 3,4-dimethylphenol was detected in two of seven rain events in Portland, OR, at 5.4 and 3.5 ng/cu m respectively. The amount associated with adsorption to particulate matter was <5% of the gas phase concn in every case(1). Not detected in either rural or urban air samples (detection limit = 0.05 ug/cu m)(2). SOURCE DOMINATED: Although found in gasoline and diesel motor exhaust, it was not detected in an Allegheny Mountain highway tunnel(3).

규제 정보

TSCA Requirements · 2건

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. 3,4-Dimethylphenol is included on this list.

Section 8(a) of TSCA requires manufacturers of this chemical substance to report preliminary assessment information concerned with production, use, and exposure to EPA as cited in the preamble in 51 FR 41329.

Used as a starting material for phenolic resins; [HSDB]

Starting materials in the phenolic resins. /Xylenols/

3,4-Dimethylphenol is found in coffee and coffee products.

U.S. Production2023: 1,000,000 - <8,500,000 lb
Consumer UsesCleaning agent
Industry UsesIntermediate
Methods of Manufacturing · 2건

The insertion of methyl groups into phenol to produce ... xylenols is a commercial process of considerable utility. The process commomly employed is methylation with methyl alcohol over a solid catalyst, generally a modified metal oxide, at temp in the range of 300-450 °C. /Xylenols/

Produced from the hydrolysis of 4-chloro-o-xylene

Use Classification · 4건

Fragrance Ingredients

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavoring Agents -> JECFA Flavorings Index

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

General Manufacturing Information · 2건

Plastics Material and Resin Manufacturing

Phenol, 3,4-dimethyl-: ACTIVE