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Product Name: |
Benzaldehyde |
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CAS: |
100-52-7 |
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MF: |
C7H6O |
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MW: |
106.12 |
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EINECS: |
202-860-4 |
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Mol File: |
100-52-7.mol |
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Liquescens punctum |
-26 ° C |
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Ferveret |
CLXXIX ° F |
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density |
1.044 g / III cm ad XX ° C (Litt.) |
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vapor densitatem, |
3.7 (VS caeli) |
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vapor pressura |
IV mm Aggaei (XLV ° C) |
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potenti |
MMCXXVII | BENZALDEHYDE |
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refractivam index |
n20 / D 1.545 (lit.) |
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Fp |
CXLV ° F |
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temp repono. |
locus temp |
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solubility |
H2O Prunus: soluble100mg / ml |
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pka |
14.90 (apud 25a) |
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forma |
tersus |
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Odor |
Velut in amygdalas deformati sunt. |
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PH |
5.9 (1g / l, H2O) |
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terminus explosive |
1.4-8.5% (V) |
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aqua Solubility |
<0.01 g / C ml at19.5 ºC |
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FreezingPoint |
-56â |
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sensitivo |
aeris sensitiva |
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Number JECFA |
22 |
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Merck Poland |
14,1058 |
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BRN |
471223 |
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Stabilitatem: |
Firmum. Combustible.Incompatible magnis oxidizing agentia fortis acidis deiciatur agentibus vapor. Caeli lumen, et humorem sensitivo. |
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InChIKey |
HUMNYLRZRPPJDN UHFFFAOYSA-N, |
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CAS DataBase Reference |
100-52-7 (CAS DataBase Reference) |
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Quaestiones NIST Reference |
Benzaldehyde (100-52-7) |
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Ratio Subcriptio quod substantia EPA |
Benzaldehyde (100-52-7) |
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aleam Codes |
xII |
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risk Denunciationes |
22 |
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Denunciationes salutem |
24 |
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RIDADR |
UN Consilium MCMXC IX / PG III |
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Germania WGK |
1 |
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RTECS |
CU4375000 |
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F |
8 |
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Autoignition Temperature |
CCCLXXIV ° F |
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Capparis |
Ita |
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HS Code |
XXI 00 MMCMXII |
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HazardClass |
9 |
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PackingGroup |
III |
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Ancipitia substantiae Data |
100-52-7 (Malo Periculosam substantias Indicium) |
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Aedes |
LD50 in mures inclusi essent, guineapigs (mg / kg) MCCC, M viva voce (Jeuner) |
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usibus |
In productione intermediatein Benzaldehyde usedas CONDITIO oeconomiae est talis ascinnamaldehyde, cinnamalalcohol et amyl- et hexylcinnamaldehyde forperfume, saponem et ciborum sapore penicillino synthetica, doxycycline, andephedrine; et quantum ad materiam araw Vindica herbicide. Itoccurs naturein, in amygdalas deformati sunt semina, apricots, cerasis et persica. It occurs in intraceamounts frumentum oleum. |
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usibus |
OPIFICIUM rubores, pigmentaria, Cinámico mandelic acida et quasi solvendo In saporibus destinato. |
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usibus |
Benzaldehyde aflavoring agente quod sit vivum liquidum est et exanguis, et quasi in nucis modum habet odor.it habet calidi (ardenti) gustum. et deterior est oxidized ad toair conquassatum crat sub lucem expositae. est miscible in volatile unguento delibuti fixedoils, sive, sive spiritus ardens; lorum spar- sit aqua solutum. Donec est synthesis obtainedby naturali olea eventum acerba amigdalinas persici et persicum nucleo. quae etiam est concentrata conquassatum aldehyde. |
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definitio |
Vrina citrina quando est distincta organicum oilwith almondlike odoris suavissimi componendum. Benzenecarbaldehyde fastidia sustinet reactionscharacteristic de aldehydes et erit summatim perstringitur a officinarum in in aldehyde theusual modi compositionis. Est usus ut a CONDITIO et tunc corviculi attrahunt cibo pasta et fabricare de antibiotics et libenter confici potest ex bythe chlorination methylbenzene et subsequent hydrolysa (dichloromethyl) benzene: C6H5CH3 + + Cl2â C6H5CHCl2 C6H5CHCl2 2H2O â € C6H5CH (OH) 2+ 2HCl C6H5CH (OH) II â € C6H5CHO + H2O Prunus. |
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Aroma limine values |
DEPREHENSIO: ppm C ppbto 4,6; Recognition: bilionem CCCXXX ad 4.1 ppm. |
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Saporem limine values |
L ad Tastecharacteristics ppm suavis, pinguis et amigdalinas cerasis et nemorosa nutty |
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Communia |
A hyalina toyellow liquido patet cum amara amygdalus, impinguabitur locusta odoris suavissimi componendum. CXLV iuxta mico punctum F. Magis denserthan aqua et dissolvi in aqua. Unde in aquis. Heavierthan aeris et vaporum generantur. In prima aleam est elit. Ut vestigia si statim contulerunt ad propagationem limit environment. Facilius ingruere et prope fluminum solo tocontaminate groundwater. Et in CONDITIO perfumemaking. |
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Agrippina Minor aqua Aeris & |
Oxidizes in aere toform concentrata conquassatum crat, est superior modice toxicus per ingestion. Inwater posse dissolvi. |
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Reactividad Profile |
A nontoxic combustibilis liquido reagat sunt reagentia oxidizing. Benzaldehyde beblanketed necesse est efficaciæ iners Gas aeris sunt in omni tempore quo Benzaldehyde is concentrata conquassatum crat per oxidizedreadily [Kirk, Othmer, 3 ed., Vol. III, MCMLXXVIII, p. DCCXXXVI] .In contactus cum acida bases Benzaldehyde subibit exothermiccondensation fortis reactionem [Sax, 9th ed., MCMXCVI, p. CCCXXVII]. Vehemens A in contactu cum peroxyacids wasobserved reactionem (Acidum peroxyformic) [giniensibus venisset, J. et al., Ber., MCMXV: XLVIII, p. MCXXXVI]. Strepitus pyrrolidine cum occurrit, Benzaldehyde et propionic acidum synthesis cum calefacta forma. |
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aleam |
Altus toxicus. |
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salutem DISCRIMEN |
Maximum Benzaldehydeexhibited moderari toxicityin amet animalium poisoningeffectdepending in mg. Ingestion 50a LX mLmay homines mortem afferebat. Oralintake largedose possit de causa tremor, gastrointestinal dolor et kidneydamage. Quod causatur tremor guineapigs compoundby experimentsindicated ingestion animalis huius sanguinis fromsmall intestinum urinevolume augeri in mures ingestion effecit somnolenceand coma. |
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ignis DISCRIMEN |
MULTUM NAPTHA numquid non facile ab igne calorem, sicut tædæ seu flammae. Explosivemixtures formare vapores in aere. Ut iter ad fontem ignitionem, et elevat nebulas omnia graviora sunt caeli emicare back.Most. Cum angustiis loci et loca humilia dilataberis collectin (cloacas Basements, lacus.) CREPITUS hazardindoors vapor, aut latebram prospicimus cloacas fecit. Runoff ad partum, ut ignis aut explosionhazard cloaca. Continentia, ut explodere, cum ardentis. Multi leves sint liquida thanwater. |
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eget Reactividad |
Reactividad withWater: non reactionem, Reactividad cum Clementine_Vulgate Materias: nullus motus; StabilityDuring Onerariis: Stabull; Acidis propter se curat ut medicamentis agens: Notpertinent; Polimerización: non pertinent; Matrix Polimerización: Notpertinent. |
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salutem Profile |
Ingestionand intraperitoneal per venenum urbis itinera. Per modum telae noxia iter. Anallergen. Acts, quod scilicet decrepitus loci Papaver. Locus contactdermatitis faciam ut contactus. Causa systematis nervosi centralis tristitia exigua portione medicatur et convulsionsin maior doses. A cutis irritationem. Cum dubiae carcinogen experimentaltumorigenic data. Nuntiavit mutationem notitia. Carros SAac. Pugnare ignis, aqua usum (quod potest uti stragulum); alcohole crystallina specie spumam, sicco eget. A strongreducing agente. Reacts violenter peroxyformic et acidum et aliis oxidizers.See aldehydes. |
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Synthesis eget |
A subsequent deest distillatoria et extractionem naturalis benzaldehydeis adeptus frombotanical fontibus; synthetically a benzyl chloride et visco et toluene byoxidation |
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Potentialis expositio |
In OPIFICIUM ofperfumes, colores, et ácido; quod solvent; In saporibus destinato. |
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storage |
Benzaldehyde putandam repositam in catenatos obsutaque continens et physicaldamage donec introducamus eos. Eget repono de substantia extra, sive in area ispreferred Caesar, cum sit intus in repono vexillum locus seu scrinium liquidsstorage flammabilia. Agi ab Benzaldehyde oxidizingmaterials. Item, usu et repono areas debet esse fumigans areas. Cum materia sit vacua periculo Containersof productresidues retinent (vapor umidus) Morbi tellus forthe pertinent monita omnia |
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naviportans |
UN1990 Benzaldehyde Hazard genus: IX: Labels: 9 a ancipitia Miscellaneous materia. |
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Ratio purificatione |
Rateof oxidation eius minuere, quae continet additives hydroquinone orcatechol benzaldehyde solet. Quod sit purificari potest nisi per eius bisulfite praeter compositis usuallydistillation (sub NITROGENIUM reducitur ad pressura) sat est. Prior est todistillation NaOH et laverunt per X% Na2CO3 (ultra quam isevolved CO2), deinde per naturam saturis et Na2SO3 H2O, ex siccitate sequitur CaSO4, aut MgSO4 CaCl2. [VII Beilstein IV 505] |
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incompatibilities |
Summa aeris reactswith formatam peroxides explosive. Violenter Reacts performic acidum oxidants aluminium ferro fundamentis phenol causa explosionhazard ignis. Si auto-May ignite addito spatio largesurface cum materia combustibilis ab aere obscuritas, non aliter dispersit in areas magnas. Reacts robigine amines, alkalies fortis bases et hydrideds ut redigo agentia activemetals. |
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Vastum dispositioni |
incineratio: addcombustible solvente, et in imbre et Incinerator afterburner. |
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Cautiones |
Quia operarius becareful benzaldehyde periculum spontaneouscombustion cum usura. Ut, si sua sponte id est ignium onto occupata pannisque obsita praecucurrit, cleaningcloths vel vestibus seu SERRAGO, terra Diatomaceous (kieselguhr), activatedcharcoal aliisve materiis confecta, cum superficies magna areas in workplaces. Ne Workersshould tractantem enim eget neque substantia inciditur cruorem eliciunt, vel ad orweld prope in quo est. Benzaldehyde nuditate ad caeli, lux, calidum, calidum calidi, ut superficies et fistularum tuarum, scintillas quasdam aperta flammas et ignitionsources se ipsa fugienda esse concedant. Debet gerunt propriis operarios et personalis apparatu protectiveclothing |
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Praeparatio Products |
2,3,5 chloride, Triphenyltetrazolium -> whitener W. lana -> Benzalacetone -> DIPHENYLPYRAZOLE, 3,5 -> Epalrestat -> Bis (dibenzylideneacetone) Palladium -> 2. [2. (4 Fluorophenyl) -2-i-oxo phenylethyl] -4-III-oxo N-phenylpentanamide yl -> L-Arginine dose -> 2. (Acetylamino), II-3-phenyl propenoicacid -> methyl 1H, indole-II-carboxylic -> TRANS-I-II-phenyl, CYCLOPROPANECARBOXYLICACID -> amino-I-IV-METHYLPIPERAZINEDIHYDROCHLORIDE monohydrate -> Nazgul XC omnia blue -> Diaveridine -> Nifedipine -> Reactive CIV blue -> Dichlorobenzylamine, 3,4 -> Tris (dibenzylideneacetone) dipalladium -> Nitrotetrazolium hyacintho chloride -> BENZYLHYDRAZINE DIHYDROCHLORIDE -> (R) - (+) - N-Benzyl-I-Phenylethylamine -> 2. ((E) -2-Hydroxy-III-phenylacryloyl) benzoicacid: XCVII% -> (E) Benzylidene-3-3H, isochromene-1,4-dione: XCVII% -> Reactive BRF omnia blue -> FLAVANONE -> Phenylglycine Dominus -> Benzenemethanol, ar-methyl-, acetate -> red ASTRAZON LAETUS 4G -> II-V-chloro amino-methanolum, diphenyl -> Magentagreencrystals -> Nazgul IX omnia Blue -> Hexylcinnamaldehyde alpha -> Mandelic DL, acidum -> N, N'-BISBENZYLIDENEBENZIDINE -> 2,4,5, TRIPHENYLIMIDAZOLE -> IV-Hydroxybenzylideneacetone -> Diphenylhydantoin, 5,5 -> 1. [2. [II-3-hydroxy ( propylamino) propoxi] phenyl] phenylpropan-3-I-onehydrochloride -> N, N'-dibenzyl ethylenediaminediacetate -> DIOXOLANE 1.3-II-IV-methanolum, phenyl, |
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et rudis materiae |
Toluene -> Natrii carbonas -> Palladii -> Carbon -> Benzyl chloride -> spodi -> carbo carbonis monoxide -> aluminium chloride hexahydrate -> Benzyl alcohol -> trioxide Molybdenum -> Ozone- -> trans-Cinnamaldehyde -> Cadmiae pHOSPHATE -> calami similiter ducentos quinquaginta oleum -> Amygdalin |
