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1-Chloro-1-propene

HCID 11536
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
590-21-6
Standard SMILES
CC=CCl
InChIKey
OWXJKYNZGFSVRC-UHFFFAOYSA-N
Molecular formula
C3H5Cl
Average molar mass
76.52 g/mol
Monoisotopic mass
76.0079779

Overview

1-chloropropylene is a colorless liquid with disagreeable odor.

Names & identifiers

Preferred name
1-Chloro-1-propene
IUPAC
1-chloroprop-1-ene
English name
1-Chloro-1-propene
Molecular formula
C3H5Cl
Molecular weight
76.52

Names & synonyms

590-21-61-Chloropropene1-Propene, 1-chloro-1-CHLORO-1-PROPENEPropenyl chlorideDTXSID5020318Propene, 1-chloro-0HXU981C24NSC-6155RefChem:431154DTXCID40809751209-675-8
Show more names
Nsc6155Wln: G1U2CH3CH=CHCl1-chloro-propen1-Chlor-1-propen1-chloro-1-propenE-1-CHLOROPROPENE
1-Chloropropylene1-chloroprop-1-eneChloropropene(Z)-Chloro-1-propeneC3H5Cl1-Propenyl Chloride3-chloro-2-propeneSCHEMBL2668

Database identifiers

CAS
590-21-6
PubChem CID
11536
DTXSID
DTXSID5020318
EC Number
209-675-8

Properties

Computed structural properties

XLogP
1.7
Topological polar surface area
0 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
0
Rotatable bonds
0
Heavy atoms
4
Formal charge
0
Complexity
22.5

Experimental & physicochemical properties

Chemical Classes · 2 items

Other Classes -> Halogenated Aliphatics, Unsaturated

Flammable agents - 4th degree

SpringerMaterials PropertiesDensity
Density0.9 (WATER= 1)
Color/FormLiquid /cis and trans isomers/
Solubility · 2 items

Sol in ether, acetone, sol in benzene, chloroform /cis and trans isomers/

Insol in water /cis and trans isomers/

Flash Point · 3 items

less than 21 °F (NFPA, 2010)

Flash point > -6 °C

greater than 21 °F (greater than -6 °C) (Closed cup)

Boiling Point35-36 °C
Vapor Pressure · 2 items

507.0 [mmHg]

507 mm Hg at 25 °C

Physical Description · 2 items

1-chloropropylene is a colorless liquid with disagreeable odor.

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Danger

H224 (17.6%): Extremely flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 17 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory InformationThe 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 LabelCombustible Liquid
Fire HazardsExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Health HazardsExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Hazards Summary · 1 item

Inhalation of low concentrations caused anesthetic effects in mice; Caused increase in stomach tumor frequency when administered to mice by gavage; [HSDB] Tumorigenic; Causes liver changes with TCLo = 168 gm/m3/30M; [RTECS] May polymerize; [CAMEO]

Reactive GroupHalogenated Organic Compounds
Reactivity AlertsHighly Flammable
Reactivity Profile

Chemistry & industry

Pharmacology

Mechanism of Action · 2 items

The transforming ability of six epoxides of structurally related chloroalkenes was /examined/ with a quantitative Syrian hamster embryo cell model. The epoxides used were cis-l-chloropropene oxide (c-CPO), trans-l-chloropropene oxide (t-CPO), cis-1,3-dichloropropene oxide, trans-1,3-dichloropropene oxide, trichloroethylene oxide (TCEO), and tetrachloroethylene oxide (PCEO). All six epoxides induced morphologic transformation of Syrian hamster embryo cells and caused cell lethality as reflected in the reduced cloning efficiency; in all instances, transformation was observed with less than 25% toxicity. The potency of the various epoxides was influenced by the difference in stability of the compounds. The results with c-CPO, t-CPO, TCEO, and PCEO were consistent with a linear dose response. The transformation results reflect the carcinogenicity of the parental chloroalkenes tested thus far. Furthermore, if the epoxides are metabolic intermediates of the chloropropene parent chloropropenes the epoxides are probably proximate carcinogens. /Chloropropene epoxides/

Six epoxides of structurally related chloroalkenes were /evaluated/ for their carcinogenicity by chronic testing in female ICR/Ha Swiss mice, 30/group. Repeated skin application three times weekly or sc injection once weekly were used for the life spans of the mice. The epoxides were: cis-l-chloropropene oxide, trans-l-chloropropene oxide, cis-1,3-dichloropropene oxide, trans-1,3-dichloropropene oxide, trichloroethylene oxide (TCEO), and tetrachloroethylene oxide (PCEO). In mouse skin, cis-l-chloropropene oxide, trans-l-chloropropene oxide, cis-1-,3-dichloropropene oxide, and trans-1,3-dichloropropene oxide induced statistically significant incidences of squamous carcinomas of the skin; TCEO did not cause any skin tumors; and PCEO resulted in three mice with benign skin tumors and one with a squamous carcinoma of the skin. Repeated sc injection of the four propene oxides induced statistically significant incidences of local tumors, mostly fibrosarcomas. This was not the case with TCEO and PCEO. The data are consistent with the carcinogenicity findings on the parent chloropropenes and suggest that the epoxides function as their activated carcinogenic intermediates. The essentially negative findings with TCEO and PCEO suggest further studies on the carcinogenicity of trichloroethylene and tetrachloroethylene.

Uses & manufacturing

Related reactions

4 records
New reaction record
HRID 697271 reaction equation
HRID 697271As reactantTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
HRID 2079927 reaction equation
HRID 2079927As reactantuspto-grants-2011_04
HRID 2079928 reaction equation
HRID 2079928As reactantuspto-grants-2011_04
HRID 2079929 reaction equation
HRID 2079929As reactantuspto-grants-2011_04

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes

Colorless liquid with a disagreeable odor; [CAMEO]

Other Experimental Properties · 2 items

MP: -134.8 °C; BP: 32.8 °C at 760 mm Hg; Density: 0.9347 at 20 °C/4 °C; Index of refraction: 1.4055 at 20 °C/D /cis-isomer/

MP: -99 °C; BP: 37.4 °C at 760 mm Hg; Density: 0.9349 at 20 °C/4 °C; Index of refraction: 1.4054 at 20 °C/D /trans-isomer/

Physicochemical properties

Melting point
-137.3 °C · -137.3°C
Boiling point
38 °C · 38 °C
Density
0.92 · 0.92
refractive index
1.4 · 1.40
Water Solubility
Insoluble in water
form
clear liquid
color
Colorless to Almost colorless
Henry's Law Constant
1.8 · 1.8×10-4 mol/(m3Pa) at 25℃, HSDB (2015)
CAS DataBase Reference
590 · 590-21-6(CAS DataBase Reference)
EWG's Food Scores
1 · 1
FDA UNII
0 HXU981C24 · 0HXU981C24
EPA Substance Registry System
1 · 1-Chloropropene (590-21-6)
Symbol(GHS)
2 · GHS02,GHS07
Signal word
Danger
Hazard statements
225 · H225-H302-H315-H319
Precautionary statements
210 · P210-P233-P240-P241+P242+P243-P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P370+P378-P403+P235-P501
Risk Statements
12 · 12-36/37/38
Safety Statements
16 · 16-26-36
RIDADR
1993 · 1993
RTECS
7175000 · UC7175000
TSCA
TSCA listed
HazardClass
3 · 3
PackingGroup
II
HS Code
2903290000 · 2903290000
Hazardous Substances Data
590 · 590-21-6(Hazardous Substances Data)
· 1 item

1-CHLOROPROPYLENE is a halogenated unsaturated aliphatic hydrocarbon. The unsaturated aliphatic hydrocarbons are generally much more reactive than the alkanes, which are saturated aliphatic hydrocarbons. Strong oxidizers may react vigorously with them. Reducing agents can react exothermically to release gaseous hydrogen. In the presence of various catalysts (such as acids) or initiators, compounds in this class can undergo very exothermic addition polymerization reactions.

Flammable LimitsLower flammable limit: 4.5% by volume; Upper flammable limit: 16% by volume
Air and Water ReactionsHighly flammable. Slightly soluble in water.
NFPA Hazard Classification · 3 items

1 - Materials that, under emergency conditions, can cause significant irritation.

4 - Materials that rapidly or completely vaporize at atmospheric pressure and normal ambient temperature or that are readily dispersed in air and burn readily.

1 - Materials that in themselves are normally stable but that can become unstable at elevated temperatures and pressures.

Hazard Classes and Categories · 2 items

Flam. Liq. 1 (17.6%)

Flammable agents - 4th degree, Reactive agents - 1st degree

Safety & protection

Fire FightingExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
First AidExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Nonfire Spill ResponseExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Disposal Methods · 1 item

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Preventive Measures · 1 item

SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

Isolation and EvacuationExcerpt from ERG Guide 128 [Flammable Liquids (Water-Immiscible)]:
Personal Protective Equipment (PPE)Excerpt 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 44(SRC), determined from a structure estimation method(2), indicates that 1-chloro-1-propene is expected to have very high mobility in soil(SRC). Volatilization of 1-chloro-1-propene from moist soil surfaces is expected to be an important fate process(SRC) given an estimated Henry's Law constant of 0.055 atm-cu m/mole(SRC), using a fragment constant estimation method(3). 1-Chloro-1-propene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 507 mm Hg(4). Biodegradation data were not available(SRC, 2007).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 44(SRC), determined from a structure estimation method(2), indicates that 1-chloro-1-propene is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 0.055 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 1 hour and 3.5 days, respectively(SRC). Measured volatilization half-lives in dilute aqueous solution (depth of 6.5 cm) range from 16 to 20.1 minutes(5,6). According to a classification scheme(7), an estimated BCF of 7(SRC), from an estimated log Kow of 2.9(8) and a regression-derived equation(9), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Biodegradation data were not available(SRC, 2007).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 1-chloro-1-propene, which has a vapor pressure of 507 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase 1-chloro-1-propene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); half-lives for this reaction in air are estimated to be 1.3 and 1.2 days(SRC) for cis- and trans-isomers, respectively, calculated from rate constants of 1.2X10-11 and 1.4X10-11 cu cm/molecule-sec at 25 °C(for cis- and trans-isomers, respectively)(SRC) that were derived using a structure estimation method(3). Vapor-phase 1-chloro-1-propene is also degraded in the atmosphere by reaction with ozone(SRC); half-lives for this reaction in air are estimated to be 14 and 7 days(SRC) for the cis- and trans-isomers, respectively, calculated from rate constants of 0.8X10-18 and 1.6X10-18 cu cm/molecule-sec at 25 °C (for cis- and trans-isomers, respectively)(SRC) that were derived using a structure estimation method(3). 1-Chloro-1-propene does not contain chromophores that absorb at wavelengths >290 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsNeurotoxin - Acute solvent syndrome
Soil Adsorption/Mobility · 1 item

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 1-chloro-1-propene can be estimated to be 44(SRC). According to a classification scheme(2), this estimated Koc value suggests that 1-chloro-1-propene is expected to have very high mobility in soil.

Human Toxicity Excerpts · 1 item

/SIGNS AND SYMPTOMS/ Symptomatology: 1. A. Inhalation, high vapor concentration: gasping, refusal to breathe, coughing, substernal pain, and extreme respiratory distress at ... concentrations over 1500 ppm. Irritation of eyes and upper respiratory mucosa appears promptly after exposure to concentrated vapors. Lacrimation and headache are prominent. Coma may occur rapidly. B. Inhalation, low vapor concentrations: central nervous depression and moderate irritation of respiratory system. 2. Dermal: severe skin irritation with marked inflammatory response of epidermis and underlying tissues. 3. Oral: acute GI distress with pulmonary congestion and edema. CNS depression, perhaps even in absence of impaired oxygen uptake. 4. By any route, possible injuries to liver, kidneys and heart. /Dichloropropenes/

Artificial Pollution Sources1-Chloro-1-propene's production during the manufacture of allyl chloride(1) may result in its release to the environment through various waste streams(SRC).
Environmental Bioconcentration · 1 item

An estimated BCF of 7 was calculated in fish for 1-chloro-1-propene(SRC), using an estimated log Kow of 2.0(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Volatilization from Water/Soil · 1 item

Measured half-lives for 1-chloro-1-propene in dilute (1 ppm, solution depth of 6.5 cm) aqueous solution ranged from 16 to 20.1 minutes(1). The time required for 50 and 90% evaporation of 1-chloro-1-propene from a dilute aqueous solution (depth of 6.5 cm) was 16 and 59 minutes, respectively(2). The Henry's Law constant for 1-chloro-1-propene is estimated as 0.055 atm-cu m/mole(SRC) using a fragment constant estimation method(3). This Henry's Law constant indicates that 1-chloro-1-propene is expected to volatilize rapidly from water surfaces(4). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(4) is estimated as 1 hour(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 3.5 days(SRC). 1-Chloro-1-propene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1-Chloro-1-propene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 507 mm Hg(5).

Non-Human Toxicity Excerpts · 2 items

/LABORATORY ANIMALS: Acute Exposure/ Toxicological investigation of 1-chloropropene, 1-chloro-2-methyl-propene, 3-chloropropene, and 3-chloro-2-methyl-propene has shown that the 1-chloro compounds are less irritating to mucous membranes than are the 3-chloro compounds. All four compounds are anesthetic to mice when inhaled in low concentrations ... . All compounds increase blood pressure in rabbits. The increase is more pronounced and more prolonged with the 3-chloro than with the 1-chloro compounds. At high concentrations all four compounds produce death in mice within a very few minutes. At lower concentrations, 3-chloropropene and 3-chloro-2-methyl-propene commonly cause death many hours after exposure, and 1-chloropropene and 1-chloro-2-methyl-propene either kill rapidly or not at all. ...

/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ A series of 15 halogenated hydrocarbons of industrial & environmental importance were tested for carcinogenicity by chronic administration by 1 or more routes in HA:ICR Swiss mice. By intragastric intubation, 1-chloropropene & 2-chloropropanal induced significant numbers of stomach tumors.

Environmental Abiotic Degradation · 1 item

Rate constants for the vapor-phase reaction of 1-chloro-1-propene with photochemically-produced hydroxyl radicals has been estimated as 1.2X10-11 and 1.4X10-11 cu cm/molecule-sec (for cis- and trans-isomers, respectively) at 25 °C(SRC) using a structure estimation method(1). These correspond to atmospheric half-lives of about 1.3 and 1.2 days, respectively, at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). The rate constant for the vapor-phase reaction of 1-chloro-1-propene with ozone has been estimated as 0.8X10-18 and 1.6X10-18 cu cm/molecule-sec (cis- and trans-isomers, respectively) at 25 °C(SRC) that was derived using a structure estimation method(1). These correspond to atmospheric half-lives of about 14 and 7 days, respectively at an atmospheric concentration of 7X10+11 ozone molecules per cu cm(2). 1-Chloro-1-propene is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(3). 1-Chloro-1-propene does not contain chromophores that absorb at wavelengths >290 nm(3) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).

Probable Routes of Human Exposure · 1 item

NIOSH (NOES Survey 1981-1983) has statistically estimated that 145 workers (3 of these are female) are potentially exposed to 1-chloro-1-propene in the USA(1). The general population may be exposed to 1-chloro-1-propene via ingestion of drinking water and dermal contact with vapors and products containing 1-chloro-1-propene(SRC). Occupational exposure may occur through inhalation or dermal contact at workplaces where 1-chloro-1-propene is produced or used(SRC).

Environmental Water ConcentrationsDRINKING WATER: 1-Chloro-1-propene was identified in drinking water at unreported concentrations and locations in the United States(1,2). 1-Chloro-1-propene was identified in drinking water samples collected in New Orleans, LA(3).
Environmental Fate/Exposure Summary · 1 item

1-Chloro-1-propene's production during the manufacture of allyl chloride may result in its release to the environment through various waste streams. If released to air, a vapor pressure of 507 mm Hg at 25 °C indicates 1-chloro-1-propene will exist solely as a vapor in the atmosphere. Vapor-phase 1-chloro-1-propene will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be approximately 1 day for both cis- and trans-isomers. Vapor-phase 1-chloro-1-propene will also be degraded in the atmosphere by reaction with ozone molecules; half-lives for this reaction in air are estimated to be 14 and 7 days for the cis- and trans-isomers, respectively. 1-Chloro-1-propene does not contain chromophores that absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight. If released to soil, 1-chloro-1-propene is expected to have very high mobility based upon an estimated Koc of 44. Volatilization from moist soil surfaces is expected to be an important fate process based upon an estimated Henry's Law constant of 0.055 atm-cu m/mole. 1-Chloro-1-propene may volatilize from dry soil surfaces based upon its vapor pressure. Biodegradation data were not available. If released into water, 1-chloro-1-propene is not expected to adsorb to suspended solids and sediment based upon the estimated Koc. Volatilization from water surfaces is expected to be an important fate process based upon this compound's estimated Henry's Law constant. Estimated volatilization half-lives for a model river and model lake are 1 hour and 3.5 days, respectively. Measured volatilization half-lives in dilute aqueous solution (average depth of 6.5 cm) ranged from 16-20.1 minutes. An estimated BCF of 7 suggests the potential for bioconcentration in aquatic organisms is low. Hydrolysis is not expected to be an important environmental fate process since this compound lacks functional groups that hydrolyze under environmental conditions. Occupational exposure may occur through inhalation or dermal contact at workplaces where 1-chloro-1-propene is produced. The general population may be exposed to 1-chloro-1-propene via ingestion of drinking water and dermal contact with vapors and products containing 1-chloro-1-propene. (SRC)

Regulatory information

DHS Chemicals of Interest (COI) · 4 items

1-Chloropropylene

1

10000

Flammable chemical that can be released at a facility.

Safety data

tsca
TSCA listed
rtecs
UC7175000
ridadr
1993
hs_code
2903290000
risk_code
12-36/37/38
Signal word
Danger
Symbol(GHS)
GHS02,GHS07
safety_code
16-26-36
hazard_class
3
packing_group
II
Hazard statements
H225-H302-H315-H319
Precautionary statements
P210-P233-P240-P241+P242+P243-P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P370+P378-P403+P235-P501
Hazardous Substances Data
590-21-6(Hazardous Substances Data)
Uses · 2 items

Used as a chemical intermediate for 1,3-Dichloropropene; Formed as byproduct in the production of allyl chloride; [HSDB]

CHEM INT FOR 1,3-DICHLOROPROPENE (PROBABLY UNISOLATED)

U.S. Production · 2 items

(1977) 4.5X10+8 G MIN-PROBABLY FOR CAPTIVE USE

Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5521]

Methods of Manufacturing · 3 items

1,2-Dichloropropane is stable at room temperature but is dehydrochlorinated by thermal or catalytic cracking to allyl chloride (107-05-1) and 1-chloro-1-propene (590-21-6).

High temperature vapor-phase chlorination of propylene ...leading to allyl chloride...leads to small amounts of 2-chloropropene and 1-chloropropene.

By treating propylene dichloride with alcoholic potassium hydroxide and fractionating from the simultaneously formed /2-chloro-1-propene/.

General Manufacturing Information · 2 items

1-Propene, 1-chloro-: ACTIVE

Produced as a by-product from the production of allyl chloride.

Applications

General DescriptionColorless liquid with disagreeable odor.

Upstream & downstream products

Downstream products

4-Acetylamino-2-(diallylamino)anisole2-Chloropropene

Suppliers24 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
上海迈瑞尔生化科技有限公司4006356688 18621169109 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
广东云星生物技术有限公司0751-18902340975/189023400307 18902340307 · [email protected]
玛雅试剂+86 (573) 82222445 (0)18006601000 452520369 · [email protected]
广东元丰化学试剂有限公司0751-2829979 13376591640 · [email protected]
TCI AMERICA800-4238616 · [email protected]
TOKYO CHEMICAL INDUSTRY CO., LTD.03-36680489 · [email protected]
TCI Europe320-37350700 · [email protected]
陕西麟邦实业有限公司17709134430 · [email protected]
北京奥秘佳得医药科技有限公司+86-13522808617 · [email protected]
上海麦克林生化科技股份有限公司15221275939 15221275939 · [email protected]
九鼎化学(上海)科技有限公司4009209199 · [email protected]
陕西缔都医药化工有限公司029-029-81120477 17792793610 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
上海贤鼎生物科技有限公司021-021-52271985 17721149837 · [email protected]
厦门盈融达化工有限公司+86-0592-6210733 · [email protected]
上海吉至生化科技有限公司021-4009004166/18616739031 18616739031 · [email protected]
TCI Chemicals (India) Pvt. Ltd.[email protected]
广东元丰化学试剂有限公司0751-2829979 13318584237 · [email protected]
广东翁江化学试剂有限公司0751-2815983 13927872582 · [email protected]
北京百灵威科技有限公司18210857532 18210857532 · [email protected]
郑州研德生物科技有限公司13298105281 · [email protected]