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p-Anissure

4-Methoxybenzoic acid Struktur
100-09-4
CAS-Nr.
100-09-4
Bezeichnung:
p-Anissure
Englisch Name:
4-Methoxybenzoic acid
Synonyma:
ANISIC ACID;4-Methoxybenzoic acid;P-ANISIC ACID;4-ANISIC ACID;P-METHOXYBENZOIC ACID;p-Anisic acid (4-Methoxybenzoic acid);FEMA 3945;Anisic;4-Methoxybenzoic;para-anisic acid
CBNumber:
CB6746524
Summenformel:
C8H8O3
Molgewicht:
152.15
MOL-Datei:
100-09-4.mol

p-Anissure Eigenschaften

Schmelzpunkt:
182-185 °C(lit.)
Siedepunkt:
275 °C
Dichte
1.385
chüttdichte
380kg/m3
Dampfdruck
0.001Pa at 25℃
FEMA 
3945 | 4-METHOXYBENZOIC ACID
Brechungsindex
1.571-1.576
Flammpunkt:
185 °C
storage temp. 
Store below +30°C.
L?slichkeit
H2O: soluble2500 parts
Aggregatzustand
Powder
pka
4.50(at 25℃)
Farbe
White to slightly gray-beige
PH
3-4 (0.3g/l, H2O, 20℃)
Geruch (Odor)
at 10.00 % in dipropylene glycol. faint putrid sweet cadaverous
Geruchsart
animal
Biologische Quelle
synthetic
Wasserl?slichkeit
Soluble in water at 20°C 0.3g/L. Soluble in alcohol, ethyl acetate and ether.
Merck 
14,666
JECFA Number
883
BRN 
508910
Henry's Law Constant
1.8×103 mol/(m3Pa) at 25℃, Abraham and Jr. (2019)
Stabilit?t:
Stable. Incompatible with strong oxidizing agents.
Major Application
food and beverages
pharmaceutical
Kosmetik-Inhaltsstoffe Funktionen
FRAGRANCE
InChI
1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)
InChIKey
ZEYHEAKUIGZSGI-UHFFFAOYSA-N
SMILES
COc1ccc(cc1)C(O)=O
LogP
1.96
CAS Datenbank
100-09-4(CAS DataBase Reference)
NIST chemische Informationen
Benzoic acid, 4-methoxy-(100-09-4)
EPA chemische Informationen
Benzoic acid, 4-methoxy- (100-09-4)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xi,Xn
R-S?tze: 36/37/38-22
S-S?tze: 26-36-24/25
WGK Germany  1
RTECS-Nr. BZ4395000
Selbstentzündungstemperatur 185 °C
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29189090
Speicherklasse 13 - Non Combustible Solids
Toxizit?t LD50 orally in Rabbit: > 5000 mg/kg
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung
Sicherheit
P261 Einatmen von Staub vermeiden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

p-Anissure Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-S?tze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Beschreibung

P-Anisic acid, also known as 4-Methoxybenzoic acid or draconic acid, is an organic acid that has a sweet flavor. It is one of the isomers of anisic acid, including m-anisic acid and o-anisic acid. The term "anisic acid" often refers to this form specifically. P-anisic acid is produced through the oxidation of p-cresyl-methyl ether.

Chemische Eigenschaften

It appears as a colorless needle crystal at room temperature. It is soluble in ethanol, ether, and chloroform, and only slightly soluble in hot water. It remains insoluble in cold water. It is used as an intermediate for aniracetam, as well as a preservative and fragrance.

Verwenden

4-Methoxybenzoic acid (p-Anisic acid) is used in oxidation and reduction of cytochrome c in solution through different self-assembled monolayers on gold electrodes using cyclic voltammetry. p-Anisic acid has antiseptic properties. It is also used as an intermediate in the preparation of more complex organic compounds.

synthetische

To obtain 4-Methoxybenzoic acid, the mole ratio of cobalt and manganese is modified and p-methoxy toluene is reacted with oxygen or an oxygen-containing gas in the presence of acetic acid. The following is the experimental procedure:1. Using n-hexyl bromide, tri (n-hexyl) amine, para-methoxy toluene with cobalt chloride hexahydrate in about 9h;
2. By a catalytic oxidation process using p-methoxy toluene and propionic acid over a catalyst comprising of CoBr2.6H2O and MnBr2.4H2O with a reaction time of 20h;
3. Through changing the mole ratio of cobalt and manganese, using p-methoxy toluene with oxygen or oxygen containing gas in the presence of acetic acid to obtain the product.

Definition

ChEBI: 4-methoxybenzoic acid is a methoxybenzoic acid substituted with a methoxy group at position C-4. It has a role as a plant metabolite. It is functionally related to a benzoic acid. It is a conjugate acid of a 4-methoxybenzoate.

Allgemeine Beschreibung

4-Methoxybenzoic acid is the sole source of carbon and energy for growth in the cultures of Nocardia sp. DSM 1069. It is effective in clearing congestion in the lungs and the respiratory tracts in conditions like asthma or bronchitis.

Biochem/physiol Actions

The cytochrome P450 enzyme CYP199A4, a heme-dependent cytochrome P450 (CYP) monooxygenase enzyme, can efficiently demethylate 4-methoxybenzoic acid. Mechanistically, O-demethylation of 4-methoxybenzoic acid occurs via hydrogen abstraction by Compound I, followed by oxygen rebound to give the hydroxylated hemiacetal which spontaneously decomposes to yield 4-hydroxybenzoic acid and formaldehyde[5].

Materials Uses

The reaction of 4-methoxybenzoic acid and substituted tin chlorides gave the corresponding substituted tin complexes. Poly(vinyl chloride) was doped with a small quantity (0.5%) of the tin complexes and homogenous thin films were made. The effects of the additives on the stability of the polymeric material on irradiation with ultraviolet light were assessed using different methods. Such additives act as efficient ultraviolet absorbers, peroxide quenchers, and hydrogen chloride scavengers[6].

Sicherheitsprofil

Poison by subcutaneous route.When heated to decomposition it emits acrid smoke andirritating vapors.

l?uterung methode

Crystallise p-anisic acid from EtOH, water, EtOH/water or toluene. The S-benzylisothiuronium salt has m 189o (from EtOH). [Beilstein 10 II 91, 10 III 280, 10 IV 346.]

p-Anissure Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


p-Anissure Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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100-09-4(p-Anissure)Verwandte Suche:


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