1-Heptene

HCID 11610CAS 25339-56-4

Basic information

Standard SMILES
C=CCCCCC
InChIKey
ZGEGCLOFRBLKSE-UHFFFAOYSA-N
Molecular formula
C7H14
Average molar mass
98.19 g/mol
Monoisotopic mass
98.10955045

Overview

N-heptene appears as a colorless liquid. Insoluble in water and much less dense than water. Vapors heavier than air. Used to make other chemicals.

Names & identifiers

Preferred name
1-Heptene
IUPAC
hept-1-ene
English name
1-Heptene
Molecular formula
C7H14
Molecular weight
98.19

Names & synonyms

1-HEPTENEHept-1-eneHEPTENEn-HepteneNSC 74130HSDB 1078EINECS 209-767-8.alpha.-HeptyleneUN2278UNII-O748KJ11V7O748KJ11V7EINECS 246-871-2
Show more names
NSC-7413025339-56-41-HEPTENE [HSDB]1-C7H14DTXSID206046625339-56-4(n-Heptene)592-76-7(1-Heptene)alpha-heptyleneHeptenes

Database identifiers

CAS
25339-56-4、592-76-7、68526-53-4、81624-04-6
PubChem CID
11610
DTXSID
DTXSID2060466
ChEBI
CHEBI:186747
UNII
O748KJ11V7
EC Number
209-767-8、246-871-2
Nikkaji
J6.763F

Properties

Computed structural properties

XLogP
4
Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
4
Heavy atoms
7

Experimental & physicochemical properties

Chemical Classes · 3 items

Other Classes -> Aliphatics, Unsaturated

Other Classes -> Aliphatics, Unsaturated

Flammable agents - 3rd degree

LipidsFatty Acyls [FA] -> Hydrocarbons [FA11]
SpringerMaterials PropertiesBoiling point
LogP · 2 items

log Kow= 3.99

3.99

Density · 3 items

0.697 at 68 °F (USCG, 1999) - Less dense than water; will float

0.6970 @ 20 °C/4 °C

0.6969 @ 20°C

Viscosity0.5 sq mm/s

Physicochemical properties

Melting point
-119.7 °C · -119.7 °C
Boiling point
93.6 °C · 93.6 °C
Density
0.697 g/cm3 · 0.6970 g/cm3
Symbol(GHS)
2 · GHS02,GHS08
Signal word
Danger
Hazard statements
225 · H225-H304

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P273, P280, P301+P316, P303+P361+P353, P331, P370+P378, P391, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 108 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

Hazard information

Regulatory Information · 6 items

Chemical: 1-Heptene

Chemical: Heptene

1-Heptene is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1-Heptene are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

Status: Active Update: 12-08-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/32442

1-Heptene: Does not have an individual approval but may be used under an appropriate group standard

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

DOT LabelFlammable Liquid
Fire Hazards · 2 items

Excerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:

· HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames.

Fire PotentialDangerous fire hazard when exposed to heat, flame, or oxidizers.
Health Hazards · 2 items

High concentrations may produce slight irritation of eyeand respiratory tract; may also act as simple asphyxiant and slight anesthetic. (USCG, 1999)

CAUTION: Petroleum crude oil (UN1267) may contain TOXIC hydrogen sulphide gas.

Hazards Summary · 2 items

General anesthetic in mouse inhalation study (60,000 mg/m3/2H); [RTECS] An irritant; [MSDSonline] See Heptene.

Members of the group of higher olefins demonstrate potential to cause mild irritation; No evidence of skin sensitization in guinea pigs or humans; Low acute toxicity by oral, inhalation, and dermal routes; Repeated dose animal studies demonstrated no reproductive, developmental, or neurological toxicity for any members of the higher olefins group; Changes in organ weights, certain clinical chemistry/hematology values, and effects to liver and kidney were observed; [OECD SIDS: Higher Olefins - 2004] An irritant; Inhalation may cause CNS depression; An aspiration hazard by ingestion; [Matheson Tri-Gas MSDS] See 1-Heptene.

Safety & protection

Fire FightingExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Accidental Release Measures · 2 items

· CALL 911. Then call emergency response telephone number on shipping paper. If shipping paper not available or no answer, refer to appropriate telephone number listed on the inside back cover.

· ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area.

First Aid · 2 items

Remove from exposure. Administer artificial respiration if needed. (USCG, 1999)

General First Aid:

Exposure Control and Personal Protection· Wear positive pressure self-contained breathing apparatus (SCBA).
Fire Fighting ProceduresTO FIGHT FIRE, USE FOAM, DRY CHEMICAL, CARBON DIOXIDE.
Nonfire Spill ResponseExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:

Toxicology

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 3,500(SRC), determined from a log Kow of 3.99(2) and a regression-derived equation(3), indicates that 1-heptene is expected to have slight mobility in soil(SRC). Volatilization of 1-heptene from moist soil surfaces is expected to be an important fate process(SRC) given a Henry's Law constant of 0.421 atm-cu m/mole(SRC) determined from a vapor pressure of 59.3 mm Hg(4) and water solubility of 18.2 mg/l at 25 °C(5). The potential for volatilization of 1-heptene from dry soil surfaces may exist(SRC) based upon this compounds vapor pressure(4). 1-Heptene's linear hydrocarbon structure would suggest that biodegradation is an important process in soil(6).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 3,500(SRC), determined from a log Kow of 3.99(2) and a regression-derived equation(3), indicates that 1-heptene is expected to adsorb to suspended solids and sediment in water(SRC). Volatilization from water surfaces is expected to occur rapidly(3) based upon the Henry's Law constant of 0.421 atm-cu m/mole(SRC) determined from a vapor pressure of 59.3 mm Hg(4) and water solubility of 18.2 mg/l at 25 °C(5). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 3 and 94 hours, respectively(SRC). According to a classification scheme(6), an estimated BCF of 630(SRC), from its log Kow(2) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is high(SRC). 1-Heptene's linear hydrocarbon structure would suggest that biodegradation is an important process in water(7).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 1-heptene, which has a vapor pressure of 59.3 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 1-heptene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 9.5 hours(SRC), calculated from its rate constant of 4.05X10-11 cu cm/molecule-sec at 25 °C(3). The rate constant for the gas-phase reaction of 1-heptene with ozone has been measured as 1.7X10-17 cu cm/molecule-sec at 25 °C(4). This corresponds to an atmospheric half-life of about 16 hours at an atmospheric concentration of 7X10+11 ozone molecules per cu cm(4).

Food Survey Values1-Heptene was identified, not quantified, in rapeseed oil commonly used for cooking(1).
Adverse Effects · 2 items

Neurotoxin - Acute solvent syndrome

Neurotoxin - Acute solvent syndrome

Effluent Concentrations · 1 item

1-Heptene was detected in the effluent of turbo jet engines operated under varying operating conditions at concns of 0-7.3 ppb(1). 1-Heptene was identified, not quantified, in the volatiles of combusted plastics used primarily for agricultural applications(2). 1-Heptene was identified in 8 of 25 air samples taken from a landfill in Staten Island, NY at a mean concn of 0.20 ppm and a max concn of 1.31 ppm(3).

Soil Adsorption/Mobility · 1 item

The Koc of 1-heptene is estimated as 3,500(SRC), using a log Kow of 3.99(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 1-heptene is expected to have slight mobility in soil(SRC).

Atmospheric Concentrations · 3 items

SOURCE DOMINATED: 1-Heptene was identified, not quantified, in the Allegheny Tunnel, PA in 1979(1). 1-Heptene was detected at a concn of 0.2 mg/cu m in the vicinity of a gasoline station(2).

URBAN/SUBURBAN: 1-Heptene was identified, not quantified, in Leningrad, Russia, Zurich, Switzerland and Houston, TX(1).

RURAL/REMOTE: 1-Heptene was identified, not quantified, in the Sierra Nevada Mountains(1).

Safety data

Signal word
Danger
Symbol(GHS)
GHS02,GHS08
Hazard statements
H225-H304
Precautionary statements
P210-P301+P310+P331

Chemistry & industry

Pharmacology

Metabolism/MetabolitesBINDING WAS INVESTIGATED OF DIFFERENT 1-ALKENES TO CYTOCHROME P450 IN MICROSOMES FROM F344 RATS.

Uses & manufacturing

Uses · 4 items

Used in the organic synthesis of flavors, perfumes, pharmaceuticals, dyes, oils, and resins; [HSDB]

Used to make other chemicals; [CAMEO] Manufactured and used strictly as component of C6-C8 distillation cut; [IUCLID] Typical uses for C6-C8 olefins include intermediates for low-molecular weight fatty acids and mercaptans; Uses for C6-C10 olefins include intermediates for plasticizer alcohols and surfactants; [OECD SIDS: Higher Olefins - 2004]

Organic synthesis

Used in the organic synthesis of flavors, perfumes, pharmaceuticals, dyes, oils, resins.

ImpuritiesAlpha-olefins of C4, C6-C15 and >C20 are by-products of oligomerization reactions.
U.S. Production2023: 10,000,000 - <50,000,000 lb
Consumer UsesIntermediate
Industry UsesIntermediate
Methods of Manufacturing · 3 items

The One-Step Ziegler Process involves the oligomerization of ethylene in the presence of trialkylaluminum at 180-220 °C and 140 atm.

The Two-Step Ziegler Process involves the oligomerization of ethylene in the presence of aluminum alkyls at 175-200 °C and 136-204 atm. Chain growth continues with the reaction of light olefins with the aluminum alkyls continuously fed in stoichiometric amounts.

High purity ethylene contacts a nickel catalyst in a butanediol reaction medium. The alpha-olefins produced, separate from the solvent because they are insoluble in the polar medium.

Suppliers50 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖北成丰化工有限公司13125175253 · [email protected]

Related reactions

15 records

Linked notes

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