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ChemicalBook >> CAS DataBase List >>Heptaldehyde

Heptaldehyde

CAS No.
111-71-7
Chemical Name:
Heptaldehyde
Synonyms
HEPTANAL;N-HEPTANAL;N-HEPTALDEHYDE;FEMA 2541;1-HEPTALDEHYDE;FEMA 2542;ENANTHALDEHYDE;HEPTYL ALDEHYDE;ENANTHAL;FEMA 2540
CBNumber:
CB2451916
Molecular Formula:
C7H14O
Molecular Weight:
114.19
MDL Number:
MFCD00007028
MOL File:
111-71-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-23 16:59:16
Product description Number Pack Size Price
Heptanal ≥95%, FCC, FG W254002 1 each $32.2
Heptaldehyde 95% H2120 1l $145
Heptaldehyde analytical standard 61696 1ml $93.6
Heptanal ≥95%, FCC, FG W254002 1 unit $31.2
Heptanal ≥95%, FCC, FG W254002 1 unit $31.2
More product size

Heptaldehyde Properties

Melting point -43 °C (lit.)
Boiling point 153 °C (lit.)
Density 0.817 g/mL at 25 °C (lit.)
vapor pressure 3 hPa (20 °C)
FEMA 2540 | HEPTANAL
refractive index n20/D 1.413(lit.)
FLAVIS Number 05.031 | Heptanal
Flash point 95 °F
storage temp. Flammables area
solubility 1.25g/l insoluble;Very slightly soluble in water, soluble in alcohol and oils.
form Powder, Crystals or Chunks
color White to light yellow-beige
Odor Green-herbaceous, vegetable-like odor
biological source synthetic
Odor Type green
explosive limit 1.1-5.2%(V)
Odor Threshold 0.00018ppm
Water Solubility insoluble
Specific Heat Capacity Cp(liquid): 2.02 J/(g·K), at 25℃
Thermal Conductivity 0.146 W/(m·K) at 25 ℃
Sensitive Hygroscopic
Merck 14,4658
JECFA Number 95
BRN 1560236
Henry's Law Constant 3.4×10-2 mol/(m3Pa) at 25℃, Brockbank (2013)
Dielectric constant 9.1(Ambient)
Stability Stable. May be light sensitive. Flammable - readily forms explosive mixtures with air. Incompatible with strong oxidizing agents, strong bases, strong reducing agents.
Major Application flavors and fragrances
Cosmetics Ingredients Functions PERFUMING
InChI 1S/C7H14O/c1-2-3-4-5-6-7-8/h7H,2-6H2,1H3
InChIKey FXHGMKSSBGDXIY-UHFFFAOYSA-N
SMILES CCCCCCC=O
LogP 2.8 at 20℃
CAS DataBase Reference 111-71-7(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) HEPTANAL
EWG's Food Scores 1
FDA UNII 92N104S3HF
NIST Chemistry Reference Heptanal(111-71-7)
EPA Substance Registry System Heptanal (111-71-7)
UNSPSC Code 85151701
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
Signal word  Warning
Hazard statements  H303-H315+H320-H335-H401-H226
Precautionary statements  P501-P273-P240-P261-P210-P233-P243-P241-P242-P271-P264-P280-P370+P378-P312-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P304+P340+P312-P403+P233-P403+P235-P405
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi,N
Risk Statements  10-36/37/38-38-50/53
Safety Statements  26-36-37-16-61-60
RIDADR  UN 3056
WGK Germany  1
RTECS  MI6900000
Autoignition Temperature 250 °C
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  2912 19 00
HazardClass  3
PackingGroup  III
Storage Class 3 - Flammable liquids
Hazard Classifications Aquatic Chronic 3
Flam. Liq. 3
Skin Irrit. 2
Hazardous Substances Data 111-71-7(Hazardous Substances Data)
Toxicity LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 5000 mg/kg
REACH Registrations Active
Limited Quantities 5.0 L (1.3 gallons) (liquid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
2
2 0

Heptaldehyde price More Price(53)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W254002 Heptanal ≥95%, FCC, FG 111-71-7 1 each $32.2 2026-04-30 Buy
Sigma-Aldrich H2120 Heptaldehyde 95% 111-71-7 1l $145 2026-04-30 Buy
Sigma-Aldrich 61696 Heptaldehyde analytical standard 111-71-7 1ml $93.6 2026-04-30 Buy
Sigma-Aldrich W254002 Heptanal ≥95%, FCC, FG 111-71-7 1 unit $31.2 2025-07-31 Buy
Sigma-Aldrich W254002 Heptanal ≥95%, FCC, FG 111-71-7 1 unit $31.2 2025-07-31 Buy
Product number Packaging Price Buy
W254002 1 each $32.2 Buy
H2120 1l $145 Buy
61696 1ml $93.6 Buy
W254002 1 unit $31.2 Buy
W254002 1 unit $31.2 Buy

Heptaldehyde Chemical Properties,Uses,Production

Uses

Heptanal or heptanaldehyde is an alkyl aldehyde. It is a colourless liquid with a strong fruity odor, which is used as precursor to components in perfumes and lubricants.

Description

Heptanal has a very strong, fatty, harsh, pungent odor and an unpleasant, fatty taste. Heptanal is obtained by distilling castor oil, preferably under reduced pressure.

Chemical Properties

Heptanal has a very strong, fatty, harsh, pungent odor and an unpleasant, fatty taste.

Chemical Properties

colourless liquid

Occurrence

Heptanal is a constituent of the essential oils of ylang-ylang, clary sage, California lemon, bitter orange, rose and hyacinth Also reported found in cocoa, buckwheat, elderberry fruit and juice and babaco fruit (Carica pentagona Heilborn)

Uses

Heptanal is used as a synthesis intermediate in the fragrances and flavors industry. It is the precursor to 1-heptanol, ethyl heptanoate and for certain lubricants.

Uses

Manufacture of 1-heptanol; ethyl oenanthate.

Uses

Labelled Heptanal. Bioconversion of heptanal to heptanol by Saccharomyces cerevisiae and effect of C source maltose.

Definition

ChEBI: Heptanal is an n-alkanal resulting from the oxidation of the alcoholic hydroxy group of heptan-1-ol to the corresponding aldehyde. An endogenous aldehyde coming from membrane lipid oxidation, it is found in the blood of lung cancer patients and has been regarded as a potential biomarker of lung cancer. It has a role as a biomarker. It is a saturated fatty aldehyde, a n-alkanal and a medium-chain fatty aldehyde.

Preparation

Obtained by distilling castor oil, preferably under reduced pressure.

Aroma threshold values

Detection: 3 to 60 ppb.

Synthesis Reference(s)

Journal of the American Chemical Society, 105, p. 6285, 1983 DOI: 10.1021/ja00358a017
The Journal of Organic Chemistry, 31, p. 3446, 1966 DOI: 10.1021/jo01348a534

General Description

A colorless, oily liquid with a penetrating fruity odor. Insoluble in water and less dense than water. Hence floats on water. Flash point near 141°F. Used to make perfumes and pharmaceuticals.

Air & Water Reactions

Flammable. Insoluble in water.

Reactivity Profile

Heptaldehyde may undergo exothermic self-condensation or polymerization reactions in the presence of acids. May generate flammable and/or toxic gases with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Is readily oxidized to give heptanoic acid. Can react with air to give first peroxo acids, and ultimately heptanoic acid. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The presence of stabilizers (antioxidants) retards autoxidation. Incompatible with strong oxidizers, bases and reducing agents.

Hazard

Combustible.

Health Hazard

May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Metabolism

Aldehyde C-7 (heptaldehyde) is readily oxidized in the animal body to the corresponding fatty acid, which then undergoes -oxidation and is eventually oxidized to carbon dioxide and water . Boyland was unable to detect pimelic acid in the urine of rats fed heptanal, indicating that the compound was probably completely oxidized in the body. The finding of tumour-inhibiting action by malonic acid supported the possibility of ω-oxidation leading to the formation of glutaric and malonic acids, although the intermediate pimelic acid was not isolated. Yoshida et al. found that heptanal was not utilized as an energy source by chicks when fed at 5% in the diet for 6 days, although the diet was palatable and caused no deaths. Direct evidence was obtained by Erwin & Deitrich for the oxidation in rat, monkey and bovine brain of heptanal and other aldehydes that may arise from biologically active amines in the brain. Aldehyde-oxidizing activity was present in all the areas of bovine brain studied. It was suggested that brain aldehyde dehydrogenase may be important in oxidizing aldehydes from exogenous sources.

Purification Methods

Dry n-heptaldehyde with CaSO4 or Na2SO4 and fractionally distil it under reduced pressure. More extensive purification is by precipitation as the bisulfite compound (formed by adding the aldehyde to saturated aqueous NaHSO3) which is filtered off and recrystallised from hot H2O. The crystals, after being filtered and washed well with H2O, are hydrolysed by adding 700mL of aqueous Na2CO3 (12.5% w/w of anhydrous Na2CO3) per 100g of aldehyde. The aldehyde is then steam distilled off, separated, dried with CuSO4 and distilled under reduced pressure in a slow stream of nitrogen. [McNesby & Davis J Am Chem Soc 76 2148 1954, Beilstein 1 H 695, 1 I 357, 1 II 750, 1 III 2844, 1 IV 3314.]

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View Lastest Price from Heptaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Heptaldehyde pictures 2026-05-28 Heptaldehyde
111-71-7
$2.00-5.00 1KG 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
Heptaldehyde pictures 2026-03-20 Heptaldehyde
111-71-7
1KG 99% 20 mt Hebei Chuanghai Biotechnology Co., Ltd
Heptaldehyde pictures 2020-01-03 Heptaldehyde
111-71-7
$1.00 1KG 99% 10000KGS Career Henan Chemical Co
  • Heptaldehyde pictures
  • Heptaldehyde
    111-71-7
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  • 99%
  • Hebei Chuanghai Biotechnology Co,.LTD
  • Heptaldehyde pictures
  • Heptaldehyde
    111-71-7
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd
1-Heptanal, Aldehyde C7, Enanthaldehyde, Oenanthaldehyde 1-Heptanal, Aldehyde C7, Enanthaldehyde, Heptanal, Oenanthaldehyde Oenanthoaldehyde Heptaldehyde,95%,stabilized Heptaldehyde, stabilized, 95% 250ML Heptaldehyde, stabilized, 95% 50ML Enanthal Enanthaldehyde Heptaldehyde Heptyl Aldehyde HEPTANAL FOR SYNTHESIS 100 ML HEPTANAL FOR SYNTHESIS 500 ML 1-Heptanal 0.2 Heptaldehyde≥ 97% (GC) HEPTALDEHYDE ENAPTHALDEHYDE N-HEPTANALDEHYDE N-HEPTYL ALDEHYDE OENANTHALDEHYDE 1-hexanecarbaldehyde Enanthic aldehyde enanthicaldehyde Enanthole HEPTANAL 92+% FCC HEPTANAL 92+% NATURAL FCC 1-HEPTALDEHYDE, STAB. HEPTANAL 97+% Heptaldehyde, stabilized, 95% n-enanthal(dehyde) n-enanthic aldehyde n-heptanal ALDEHYD C 7 (HEPTANAL) HEPTANAL, NATURAL femanumber2541 heptan-1-al n-C6H13CHO Oenanthal Oenanthaldehyd Oenanthic aldehyde oenanthicaldehyde Oenanthol Heptanal> Heptaldehyde ISO 9001:2015 REACH heptanal (aldehyde C-7) 111-71-7 Heptaldehyde HEPTALDEHYDE For Synthesis 1-Heptanal, Aldehyde C7, Enanthaldehyde, Heptaldehyde, Oenanthaldehyde HEPTALDEHYDE ,95% HEPTYL ALDEHYDE ENANTHAL ENANTHALDEHYDE ALDEHYDE C-7 1-HEPTANAL N-HEPTALDEHYDE Heptaldehyd Heptanaldehyde standard for GC,≥98%(GC) Heptaldehyde Solution in Acetonitrile Levodropropizine Impurity 32 1-HEPTALDEHYDE FEMA 2540 FEMA 2541
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