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Category: natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
| Assay: | 95.00 to 100.00 %
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| Food Chemicals Codex Listed: | No |
| Specific Gravity: | 0.77800 to 0.78500 @ 20.00 °C.
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| Pounds per Gallon - (est).: | 6.481 to 6.540
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| Refractive Index: | 1.37800 to 1.38100 @ 20.00 °C.
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| Flash Point: | 4.00 °F. TCC ( -15.56 °C. )
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| Soluble in: |
| | water, 1.209e+004 mg/L @ 25 °C (est) |
Organoleptic Properties:
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| Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Safety Information:
| Preferred SDS: View |
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| Hazards identification |
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| Classification of the substance or mixture |
| GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
| None found. |
| GHS Label elements, including precautionary statements |
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| Pictogram | |
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| Hazard statement(s) |
| None found. |
| Precautionary statement(s) |
| None found. |
| Oral/Parenteral Toxicity: |
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Not determined
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| Dermal Toxicity: |
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Not determined
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| Inhalation Toxicity: |
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Not determined
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Safety in Use Information:
| Category: | natural substances and extractives |
| Recommendation for pivaldehyde usage levels up to: | | | not for fragrance use.
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| Recommendation for pivaldehyde flavor usage levels up to: |
| | not for flavor use.
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Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| 2,2- | dimethyl propanal | | alpha,alpha- | dimethyl propanal | | 2,2- | dimethyl propionaldehyde | | alpha,alpha- | dimethyl propionaldehyde | | 2,2- | dimethylpropanal | | 2,2- | dimethylpropionaldehyde | | neo | pentanal | | | pivalic aldehyde | | | propanal, 2,2-dimethyl- | | | trimethyl acetaldehyde |
Articles:
| PubMed: | Chemoselectivity and stereoselectivity of cyclisation pathways leading to bicyclic tetramates controlled by ring-chain tautomerisation in thiazolidines. |
| PubMed: | Divinyl BODIPY derivative: Synthesis, photophysical properties, crystal structure, photostability and bioimaging. |
| PubMed: | Double stereodifferentiation in the catalytic asymmetric aziridination of imines prepared from α-chiral amines. |
| PubMed: | Asymmetric synthesis and evaluation of a hydroxyphenylamide voltage-gated sodium channel blocker in human prostate cancer xenografts. |
| PubMed: | Synthesis of P-stereogenic compounds via kinetic deprotonation and dynamic thermodynamic resolution of phosphine sulfides: opposite sense of induction using (-)-sparteine. |
| PubMed: | Analysis of an asymmetric addition with a 2:1 mixed lithium amide/n-butyllithium aggregate. |
| PubMed: | Diastereomeric Reissert compounds of isoquinoline and 6,7-dimethoxy-3,4-dihydroisoquinoline in stereoselective synthesis. |
| PubMed: | Origin of syn/anti diastereoselectivity in aldehyde and ketone crotylation reactions: a combined theoretical and experimental study. |
| PubMed: | Gas-phase synthesis and reactivity of the organomagnesates [CH3MgL2]- (L = Cl and O2CCH3): from ligand effects to catalysis. |
| PubMed: | Cinchona alkaloid-lewis acid catalyst systems for enantioselective ketene-aldehyde cycloadditions. |
| PubMed: | Reactions of superoxo and oxo metal complexes with aldehydes. Radical-specific pathways for cross-disproportionation of superoxometal ions and acylperoxyl radicals. |
| PubMed: | Rate acceleration of the Baylis-Hillman reaction in polar solvents (water and formamide). Dominant role of hydrogen bonding, not hydrophobic effects, is implicated. |
| PubMed: | Copper(II) complexes of novel N-alkylated derivatives of cis,cis-1,3,5-triaminocyclohexane. 1. Preparation and structure. |
| PubMed: | Asymmetric strecker synthesis of alpha-amino acids via a crystallization-induced asymmetric transformation using (R)-phenylglycine amide as chiral auxiliary. |
| PubMed: | Synthesis of Homoleptic Neopentoxide and Hydrido-Neopentoxide Trirhenium(III) Clusters. |
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