Naturalis vanillin eugenol ex codice est scriptor syndrome 121-33-5Natural vanillin isobutyrate codice est scriptor syndrome 20665-85-4
Product Name: |
naturalis vanillin |
Synonym: |
Vanillincas: 121-33-5: EugenolEP impuritas H. VANILLINE: VANILLIC aldehyde, VANILLIN, vanilla, Vanillinum: Vanilin |
CAS: |
121-33-5 |
MF: |
C8H8O3 |
MW: |
152.15 |
EINECS: |
204-465-2 |
Mol File: |
121-33-5.mol |
|
Liquescens punctum |
81-83 ° C (Litt.) |
Ferveret |
CLXX ° mmHg C15 (lit.) |
density |
1.06 |
vapor densitatem, |
5.3 (VS caeli) |
vapor pressura |
> 0.01 mm Aggaei (XXV ° C) |
potenti |
MMMCVII | VANILLIN |
refractivam index |
1.4850 (estimate) |
Fp |
CXLVII ° F |
temp repono. |
armarium frigidarium |
solubility |
methanolum: 0.1 g / ml, liquet |
forma |
crystallinum pulveris |
pka |
7,396 pkA ± 0.004 (0.00 H2OI = T = ± 1.0 25.0) (PRAEIUDICATUS) |
color |
Albis vel pallide flavo |
PH |
4.3 (10g / l, H2O, 20a) |
aqua Solubility |
X g / L (ºC XXV) |
sensitivo |
Aeris & LightSensitive |
Merck Poland |
14,9932 |
Number JECFA |
889 |
BRN |
472792 |
Stabilitatem: |
Firmum. Maydiscolour aspirante lucem. Humorem, sensitivo. Strongoxidizing contra mentem agentium, Sodium peroxide. |
CAS DataBase Reference |
121-33-5 (CAS DataBase Reference) |
Quaestiones NIST Reference |
Benzaldehyde,-III-IV-hydroxy methoxy- (121-33-5) |
Ratio Subcriptio quod substantia EPA |
Vanillin (121-33-5) |
aleam Codes |
X, XI |
risk Denunciationes |
22-36 / XXXVII / 38-36 |
Denunciationes salutem |
XXIV / 25-22-37 / 39-26-36 / XXXVII / XXXIX |
RIDADR |
UN Consilium MMCMXXIV III / VIII / PG II |
Germania WGK |
1 |
RTECS |
YW5775000 |
Autoignition Temperature |
> CD ° F |
Capparis |
Ita |
HazardClass |
3/8 |
PackingGroup |
II |
HS Code |
29124100 |
Ancipitia substantiae Data |
121-33-5 (Malo Periculosam substantias Indicium) |
Aedes |
LD50 viva apud mures inclusi essent, Guinea porcos: MDLXXX, MCD mg / kg (Jeuner) |
proprietas eget |
Alba needlecrystal cum fragrantiam. Solutum in aqua temporibus CXXV, XX et II temporibus ofethylene glycol XCV% of tempore ethanol, in chloroform posse dissolvi. |
Properties eget |
Vanillin acharacteristic habet, alba, vanilla, sicut est valde dulcis saporem odorem nostrum. |
Properties eget |
Alba, crystallineneedles; SUBDULCIS odor. CXXV partes aquae solubiles, in Glycerol partibus XX et II partes XCV% sive spiritus ardens; et ex aethere solutum in chloroform. Combustibilis ab aere obscuritas. |
Properties eget |
Alba aut crepito, qui acus vel crystallinum pulveris mobilitate ingenii sweettaste sapore et vanilla. |
Properties eget |
Vanillin inmany inventus est essentialis olea et cibis delectentur, sed hoc non est de necessitate saepius odore oraroma. Sed hoc non est ex odore determinare essentialis olea et extractsfrom Vanilla planifolia, et Vanilla tahitensis laetum siliqua quassante quod dictum est per maturis formedduring enzymatic FISSIO est glycosides. |
res |
Vanillin occurswidely in natura; non est relatus in essential Javacitronella oleum ex (Cymbopogon nardus Rendl.), in quìdem, Peru balsamo simul scidit oiland stercoris columbarum maxime vanilla (Vanilla planifolia, V. tahitensis, pompona V.), coluerunt magis quam XL varietates vanilla, vanillin plantis attrahunt sicut et praesens Glucosum, et vanillin. Referuntur in guava, feyoa fructum, bacae tamnum et asparagus et PORRUM, cinnamo, gingiberi, Scoticis spearmint oleum, nutmeg, rigidas et siliginis panem, butyrum, lac, innitatur et fatty piscis curatus suilla, cervisiam, cognac, whiskeys, sherry, vinum vina rum Cocos, capulus tea roastbarley, popcorn, oatmeal, Cloudberry passionis fructum fabam Tamarind, dillherb et semen tuum frumentum oleum brasii peucedani, elderberry, loquat, Borbonio andTahiti vanilla et pancratium radix. |
usibus |
Vanillin aflavorant est artificialis seu factum ex synthetica vanilla quæ non possunt ex fromlignin pasce sero pingui sulfite syntheti- et retuli ibi localiter a processionaliter guaiacoland eugenol. et related productum, ethyl vanillin habet tres unum, halftimes CONDITIO in virtute vanillin. et vanillin refers to the ingredient in primaryflavor vanilla, quam adeptus est per extractionem, faba quoque ex thevanilla. vanillin adhibetur, pro vanilla extract, withapplication in glacies crepito, demerita, arte pistoria, ad quas potiones aut 60a CCXX ppm. |
usibus |
Andanalytical tenui media. |
usibus |
Pharmaceutic auxilium (saporem). Ut a CONDITIO agens CUPPEDIAE, quas potiones et cibos animalfeeds. Fragance sapor et aromatibus uterentur. Quia tenui synthesis. OfL fonte, dopa. |
usibus |
Et primarycomponent extract de faba quoque Vanilla. |
usibus |
Naturaliter ciborum varietate plantarum Vanillin.Occurs intitulatum ut lacus; majorcommercial vanillin natura fons sit faba quoque de vanilla extract.Synthetically productum mole illuc in-m-fundatur Lignina byproduct de paperprocesses aut ex guaicol. |
definitio |
ChEBI: A genus of the membrum benzaldehydes de transmigratione, et yl hydroxy substituents atpositions III et IV respectively. |
Aroma limine values |
DEPREHENSIO: XXIX: ppm bilionem to1.6; recognition: IV: ppm |
Saporem limine values |
Ppm Tastecharacteristics ad X; suavis, ut typical-vanilla, IBISCUM, cremeae, Alcaloide, caramellic cum pulveream simpliciter. |
Agrippina Minor aqua Aeris & |
Oxidizes onexposure tardius ad aerem. . Leviter aqua solutum. |
Reactividad Profile |
Vanillin potest reactviolently cum Br2, HClO4, kalium-tert-butoxide (methyl-tert-benzene NaOH +), (+ T formic acid (NO3) III). . Aldehyde Vanillin est. Aldehydes arereadily Oxidized ad carboxylate acida. Flammabiles et / vel aregenerated toxicus vapores e combinatione cum aldehydes Azo, Diazo componit, dithiocarbamates, nitrides et fortis reducing agentibus. Aldehydes reactwith caeli possunt dare primum peroxo acida, si ad ultimum carboxylate acida. Theseautoxidation rationes profectae sunt activated a lumine, catalyzed oftransition ex sales metallorum et autocatalytic autem (per ea quae per catalyzed thereaction). |
ignis DISCRIMEN |
Mico punctum notitia forVanillin non funguntur, quamvis hoc probabiliter Vanillin combustibilis ab aere obscuritas. |
salutem Profile |
Et mediocri toxicus byingestion, intraperitoneal, telae et intravenous routes.Experimental set effectus. Mutationem notitia humana relata. Cum Br2 reactviolently potest, HClO4, kalium-tert-butoxide, tert- chlorobenzene + NaOH, formic acid + thallium nitrate. Corrumpi autem succensa emitsacrid exagitandis fumi odor. Vide etiam aldehydes. |
Synthesis eget |
Ex vastum (liquor), et lignum pulpam industria; sulfite in solitudinem et extrahitur liquor vanillin cum benzene aftersaturation CO2 est. Et per Vanillin derivednaturally fermentum. |
storage |
Et lux caeli in humida oxidizesslowly Vanillin affectus. |
Ratio purificatione |
Crystallize vanillinfrom EtOH aquam et aquea, non autem per destillationem in vacuo. [Beilstein IV1763 VIII.] |
incompatibilities |
Withacetone esse formatam a coloribus compositis. A practicallyinsoluble compositis, in ethanol praeservatum plasmatus est et GLYCERINUM. |
Status regulatory |
Gras listed.Included per FDA Inactive Ingredients Database (solutions oris, suspensiones, syrupis, loculos tabulamque lacerto). Nonparenteral medicineslicensed includitur in in UK. Index includitur in Canadian bonus Non medicinalIngredients. |